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{{Short description|Type of tissue death by a lack of blood supply}} {{Short description|Type of tissue death by infection or lack of blood supply}}
{{Other uses}} {{Other uses}}


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| alt = | alt =
| caption = Dry gangrene affecting the toes as a result of ] | caption = Dry gangrene affecting the toes as a result of ]
| field = ], ] | field = ], ], ]
| symptoms = Change in skin color to red or black, numbness, pain, skin breakdown, coolness<ref name=NHS2015Sym/> | symptoms = Change in skin color to red or black, numbness, pain, skin breakdown, coolness<ref name=NHS2015Sym/>
| complications = ], ]<ref name=NHS2015Sym/><ref name=Pt2014/> | complications = ], ]<ref name=NHS2015Sym/><ref name=Pt2014/>
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| deaths = | deaths =
}} }}
<!-- Definition and symptoms --> ]<!-- Definition and symptoms -->
'''Gangrene''' is a type of ] caused by a ].<ref name=NHS2015Over>{{cite web|title=Gangrene|url=https://www.nhs.uk/conditions/gangrene/|website=NHS|access-date=12 December 2017|date=13 October 2015}}</ref> Symptoms may include a change in skin color to red or black, numbness, swelling, pain, skin breakdown, and coolness.<ref name=NHS2015Sym/> The feet and hands are most commonly affected.<ref name=NHS2015Sym>{{cite web|title=Gangrene Symptoms|url=https://www.nhs.uk/conditions/gangrene/symptoms/|website=NHS|access-date=12 December 2017|date=13 October 2015}}</ref> If the gangrene is caused by an infectious agent, it may present with a ] or ].<ref name=NHS2015Sym/> '''Gangrene''' is a type of ] caused by a ].<ref name=NHS2015Over>{{cite web|title=Gangrene|url=https://www.nhs.uk/conditions/gangrene/|website=NHS|access-date=12 December 2017|date=13 October 2015}}</ref> Symptoms may include a change in skin color to red or black, numbness, swelling, pain, skin breakdown, and coolness.<ref name=NHS2015Sym/> The feet and hands are most commonly affected.<ref name=NHS2015Sym>{{cite web|title=Gangrene Symptoms|url=https://www.nhs.uk/conditions/gangrene/symptoms/|website=NHS|access-date=12 December 2017|date=13 October 2015}}</ref> If the gangrene is caused by an infectious agent, it may present with a ] or ].<ref name=NHS2015Sym/>


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<!-- Treatment --> <!-- Treatment -->
Treatment may involve surgery to remove the dead tissue, ] to treat any infection, and efforts to address the underlying cause.<ref name=NHS2015Tx/> Surgical efforts may include ], ], or the use of ].<ref name=NHS2015Tx/> Efforts to treat the underlying cause may include ] or ].<ref name=NHS2015Tx>{{cite web|title=Gangrene Treatment|url=https://www.nhs.uk/conditions/gangrene/treatment/|website=NHS|access-date=12 December 2017}}</ref> In certain cases, ] may be useful.<ref name=NHS2015Tx/> How commonly the condition occurs is unknown.<ref name=Pt2014>{{cite web|title=Gangrene|url=https://patient.info/doctor/gangrene|website=patient.info|access-date=12 December 2017|date=12 March 2014}}</ref> Treatment may involve surgery to remove the dead tissue, ] to treat any infection, and efforts to address the underlying cause.<ref name=NHS2015Tx/> Surgical efforts may include ], ], or the use of ].<ref name=NHS2015Tx/> Efforts to treat the underlying cause may include ] or ].<ref name=NHS2015Tx>{{cite web|title=Gangrene Treatment|url=https://www.nhs.uk/conditions/gangrene/treatment/|website=NHS|access-date=12 December 2017}}</ref> In certain cases, ] may be useful.<ref name=NHS2015Tx/> How commonly the condition occurs is unknown.<ref name=Pt2014>{{cite web|title=Gangrene|url=https://patient.info/doctor/gangrene|website=patient.info|access-date=12 December 2017|date=12 March 2014}}</ref>

== Etymology ==
The ] of gangrene derives from the ] word {{lang|la|gangraena}} and from the ] {{transl|grc|gangraina}} (γάγγραινα), which means "] of tissues".<ref>Liddell & Scott's Lexicon, Oxford University Press, 1963 edition</ref>


==Signs and symptoms== ==Signs and symptoms==
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===Dry gangrene=== ===Dry gangrene===
Dry gangrene is a form of ] that develops in ] ], where the blood supply is inadequate to keep tissue viable. It is not a disease itself, but a symptom of other diseases.<ref>{{cite book|last1=Smith|first1=Tyler|title=Gangrene Management: Today and Tomorrow|date=2015|publisher=Hayle Medical|isbn=978-1632412232}}{{page needed|date=March 2019}}</ref> The term ''dry'' is used only when referring to a limb or to the gut (in other locations, this same type of necrosis is called an infarction, such as ]).<ref>{{cite book |last1=Cross |first1=Simon |title=Underwood's Pathology: A Clinical Approach |date=2018 |publisher=Elsevier Health Sciences |isbn=9780702072109 |page=124 |edition=7th |url=https://books.google.com/books?id=1jtRDwAAQBAJ |access-date=8 April 2020}}</ref> Dry gangrene is often due to ], but can be due to ]. As a result, people with arteriosclerosis, high cholesterol, diabetes and smokers commonly have dry gangrene.<ref name=":0" /> The limited oxygen in the ischemic limb limits ] and bacteria fail to survive. The affected part is dry, shrunken, and dark reddish-black. The line of separation usually brings about complete separation, with eventual falling off of the gangrenous tissue if it is not removed surgically, a process called ].<ref name=":0">{{Cite journal|last=Al Wahbi|first=Abdullah|date=2018-06-01|title=Autoamputation of diabetic toe with dry gangrene: a myth or a fact?|journal=Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy|volume=11|pages=255–264|doi=10.2147/DMSO.S164199|issn=1178-7007|pmc=5987754|pmid=29910628}}</ref> Dry gangrene is a form of ] that develops in ] ], where the blood supply is inadequate to keep tissue viable. It is not a disease itself, but a symptom of other diseases.<ref>{{cite book|last1=Smith|first1=Tyler|title=Gangrene Management: Today and Tomorrow|date=2015|publisher=Hayle Medical|isbn=978-1632412232}}{{page needed|date=March 2019}}</ref> The term ''dry'' is used only when referring to a limb or to the gut (in other locations, this same type of necrosis is called an infarction, such as ]).<ref>{{cite book |last1=Cross |first1=Simon |title=Underwood's Pathology: A Clinical Approach |date=2018 |publisher=Elsevier Health Sciences |isbn=9780702072109 |page=124 |edition=7th |url=https://books.google.com/books?id=1jtRDwAAQBAJ |access-date=8 April 2020}}</ref> Dry gangrene is often due to ], but can be due to ]. As a result, people with atherosclerosis, high cholesterol, diabetes and smokers commonly have dry gangrene.<ref name=":0" /> The limited oxygen in the ischemic limb limits ] and bacteria fail to survive. The affected part is dry, shrunken, and dark reddish-black. The line of separation usually brings about complete separation, with eventual falling off of the gangrenous tissue if it is not removed surgically, a process called ].<ref name=":0">{{Cite journal|last=Al Wahbi|first=Abdullah|date=2018-06-01|title=Autoamputation of diabetic toe with dry gangrene: a myth or a fact?|journal=Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy|volume=11|pages=255–264|doi=10.2147/DMSO.S164199|issn=1178-7007|pmc=5987754|pmid=29910628 |doi-access=free }}</ref>


Dry gangrene is the result of chronic ] without ]. If ischemia is detected early, when ]s rather than gangrene are present, the process can be treated by ] (via vascular bypass or angioplasty).<ref>{{cite journal |vauthors=Aiello A, Anichini R, Brocco E, Caravaggi C, Chiavetta A, Cioni R, Da Ros R, De Feo ME, Ferraresi R, Florio F, Gargiulo M, Galzerano G, Gandini R, Giurato L, Graziani L, Mancini L, Manzi M, Modugno P, Setacci C, Uccioli L |title=Treatment of peripheral arterial disease in diabetes: a consensus of the Italian Societies of Diabetes (SID, AMD), Radiology (SIRM) and Vascular Endovascular Surgery (SICVE) |journal=Nutr Metab Cardiovasc Dis |volume=24 |issue=4 |pages=355–69 |year=2014 |pmid=24486336 |doi=10.1016/j.numecd.2013.12.007 |doi-access=free }}</ref> However, once gangrene has developed, the affected tissues are not salvageable.<ref>{{cite journal|last1=Gerhard-Herman|first1=MD|last2=Gornik|first2=HL|last3=Barrett|first3=C|last4=Barshes|first4=NR|last5=Corriere|first5=MA|last6=Drachman|first6=DE|last7=Fleisher|first7=LA|last8=Fowkes|first8=FG|last9=Hamburg|first9=NM|last10=Kinlay|first10=S|last11=Lookstein|first11=R|last12=Misra|first12=S|last13=Mureebe|first13=L|last14=Olin|first14=JW|last15=Patel|first15=RA|last16=Regensteiner|first16=JG|last17=Schanzer|first17=A|last18=Shishehbor|first18=MH|last19=Stewart|first19=KJ|last20=Treat-Jacobson|first20=D|last21=Walsh|first21=ME|title=2016 AHA/ACC Guideline on the Management of Patients With Lower Extremity Peripheral Artery Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines.|journal=Circulation|date=2017|volume=135|issue=12|pages=e726–79|doi=10.1161/CIR.0000000000000471|pmid=27840333|pmc=5477786}}</ref> Because dry gangrene is not accompanied by infection, it is not as ] as gas gangrene or wet gangrene, both of which have a risk of sepsis. Over time, dry gangrene may develop into wet gangrene if an infection develops in the dead tissues.<ref>{{cite book|last1=Nather|first1=Aziz|title=The diabetic foot|date=2013|isbn=978-9814417006}}</ref> Dry gangrene is the result of chronic ] without ]. If ischemia is detected early, when ]s rather than gangrene are present, the process can be treated by ] (via vascular bypass or angioplasty).<ref>{{cite journal |vauthors=Aiello A, Anichini R, Brocco E, Caravaggi C, Chiavetta A, Cioni R, Da Ros R, De Feo ME, Ferraresi R, Florio F, Gargiulo M, Galzerano G, Gandini R, Giurato L, Graziani L, Mancini L, Manzi M, Modugno P, Setacci C, Uccioli L |title=Treatment of peripheral arterial disease in diabetes: a consensus of the Italian Societies of Diabetes (SID, AMD), Radiology (SIRM) and Vascular Endovascular Surgery (SICVE) |journal=Nutr Metab Cardiovasc Dis |volume=24 |issue=4 |pages=355–69 |year=2014 |pmid=24486336 |doi=10.1016/j.numecd.2013.12.007 |doi-access=free }}</ref> However, once gangrene has developed, the affected tissues are not salvageable.<ref>{{cite journal|last1=Gerhard-Herman|first1=MD|last2=Gornik|first2=HL|last3=Barrett|first3=C|last4=Barshes|first4=NR|last5=Corriere|first5=MA|last6=Drachman|first6=DE|last7=Fleisher|first7=LA|last8=Fowkes|first8=FG|last9=Hamburg|first9=NM|last10=Kinlay|first10=S|last11=Lookstein|first11=R|last12=Misra|first12=S|last13=Mureebe|first13=L|last14=Olin|first14=JW|last15=Patel|first15=RA|last16=Regensteiner|first16=JG|last17=Schanzer|first17=A|last18=Shishehbor|first18=MH|last19=Stewart|first19=KJ|last20=Treat-Jacobson|first20=D|last21=Walsh|first21=ME|title=2016 AHA/ACC Guideline on the Management of Patients With Lower Extremity Peripheral Artery Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines.|journal=Circulation|date=2017|volume=135|issue=12|pages=e726–79|doi=10.1161/CIR.0000000000000471|pmid=27840333|pmc=5477786}}</ref> Because dry gangrene is not accompanied by infection, it is not as ] as gas gangrene or wet gangrene, both of which have a risk of sepsis. Over time, dry gangrene may develop into wet gangrene if an infection develops in the dead tissues.<ref>{{cite book|last1=Nather|first1=Aziz|title=The diabetic foot|date=2013|publisher=World Scientific |isbn=978-9814417006}}</ref>


] is a risk factor for peripheral vascular disease, thus for dry gangrene, but also a risk factor for wet gangrene, particularly in patients with poorly controlled blood sugar levels, as elevated serum glucose creates a favorable environment for bacterial infection.<ref>{{cite journal|last1=Vayvada|first1=H|last2=Demirdover|first2=C|last3=Menderes|first3=A|last4=Karaca|first4=C|title=Necrotising fasciitis in the central part of the body: diagnosis, management and review of the literature.|journal=International Wound Journal|date=August 2013|volume=10|issue=4|pages=466–72|pmid=22694053|doi=10.1111/j.1742-481x.2012.01006.x|s2cid=5693425|pmc=7950796}}</ref> ] is a risk factor for peripheral vascular disease, thus for dry gangrene, but also a risk factor for wet gangrene, particularly in patients with poorly controlled blood sugar levels, as elevated serum glucose creates a favorable environment for bacterial infection.<ref>{{cite journal|last1=Vayvada|first1=H|last2=Demirdover|first2=C|last3=Menderes|first3=A|last4=Karaca|first4=C|title=Necrotising fasciitis in the central part of the body: diagnosis, management and review of the literature.|journal=International Wound Journal|date=August 2013|volume=10|issue=4|pages=466–72|pmid=22694053|doi=10.1111/j.1742-481x.2012.01006.x|s2cid=5693425|pmc=7950796}}</ref>
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Wet, or infected, gangrene is characterized by thriving bacteria and has a poor ] (compared to dry gangrene) due to sepsis resulting from the free communication between infected fluid and circulatory fluid. In wet gangrene, the tissue is infected by ] microorganisms ('']'' or '']'', for example), which cause tissue to swell and emit a foul odor. Wet gangrene usually develops rapidly due to blockage of venous (mainly) or arterial blood flow.<ref name=":0" /> The affected part is saturated with stagnant blood, which promotes the rapid growth of bacteria. The toxic products formed by bacteria are absorbed, causing systemic manifestation of sepsis and finally death. The affected part is edematous, soft, putrid, rotten, and dark.{{citation needed|date=February 2021}} Wet, or infected, gangrene is characterized by thriving bacteria and has a poor ] (compared to dry gangrene) due to sepsis resulting from the free communication between infected fluid and circulatory fluid. In wet gangrene, the tissue is infected by ] microorganisms ('']'' or '']'', for example), which cause tissue to swell and emit a foul odor. Wet gangrene usually develops rapidly due to blockage of venous (mainly) or arterial blood flow.<ref name=":0" /> The affected part is saturated with stagnant blood, which promotes the rapid growth of bacteria. The toxic products formed by bacteria are absorbed, causing systemic manifestation of sepsis and finally death. The affected part is edematous, soft, putrid, rotten, and dark.{{citation needed|date=February 2021}}


Because of the high mortality associated with infected gangrene (about 80% without treatment and 20% with treatment), an emergency salvage amputation, such as a ], is often needed to limit systemic effects of the infection.<ref name=CochAmp/> Such an amputation can be converted to a formal amputation, such as a ].<ref name=CochAmp>{{cite journal|last1=Tisi|first1=PV|last2=Than|first2=MM|title=Type of incision for below knee amputation.|journal=The Cochrane Database of Systematic Reviews|date=8 April 2014|volume=4|issue=4|pages=CD003749|pmid=24715679|doi=10.1002/14651858.CD003749.pub3|pmc=7154343}}</ref> Because of the high mortality associated with infected gangrene (about 80% without treatment and 20% with treatment), an emergency salvage amputation, such as a ], is often needed to limit systemic effects of the infection.<ref name=CochAmp/> Such an amputation can be converted to a formal amputation, such as a ].<ref name=CochAmp>{{cite journal|last1=Tisi|first1=PV|last2=Than|first2=MM|title=Type of incision for below knee amputation.|journal=The Cochrane Database of Systematic Reviews|date=8 April 2014|volume=2014|issue=4|pages=CD003749|pmid=24715679|doi=10.1002/14651858.CD003749.pub3|pmc=7154343}}</ref>


===Gas gangrene=== ===Gas gangrene===
{{Main|Gas gangrene}} {{Main|Gas gangrene}}
Gas gangrene is a bacterial infection that produces gas within tissues. It can be caused by '']'', most commonly ]-producing ''C. perfringens'', or various nonclostridial species.<ref name=Yang2015 /><ref name="Sakurai">{{cite journal|last1=Sakurai|first1=J.|last2=Nagahama|first2=M.|last3=Oda|first3=M.|s2cid=12940936|title=''Clostridium perfringens'' alpha-toxin: characterization and mode of action|journal=Journal of Biochemistry|date=November 2004|volume=136|issue=5|pages=569–74|doi=10.1093/jb/mvh161|pmid=15632295}}</ref> Infection spreads rapidly as the gases produced by the bacteria expand and infiltrate healthy tissue in the vicinity. Because of its ability to quickly spread to surrounding tissues, gas gangrene should be treated as a ]. This is the most fatal form of gangrene, highly so, even with treatment (50%), and can be 100% fatal if left untreated.{{citation needed|date=February 2021}} Gas gangrene is a bacterial infection that produces gas within tissues. It can be caused by '']'', most commonly ]-producing ''C. perfringens'', or various nonclostridial species.<ref name=Yang2015 /><ref name="Sakurai">{{cite journal|last1=Sakurai|first1=J.|last2=Nagahama|first2=M.|last3=Oda|first3=M.|s2cid=12940936|title=''Clostridium perfringens'' alpha-toxin: characterization and mode of action|journal=]|date=November 2004|volume=136|issue=5|pages=569–74|doi=10.1093/jb/mvh161|pmid=15632295}}</ref> Infection spreads rapidly as the gases produced by the bacteria expand and infiltrate healthy tissue in the vicinity. Because of its ability to quickly spread to surrounding tissues, gas gangrene should be treated as a ].


Gas gangrene is caused by bacterial ]-producing clostridial species, which are mostly found in soil, and other anaerobes such as '']'' and anaerobic ]. These environmental bacteria may enter the muscle through a wound and subsequently proliferate in necrotic tissue and secrete powerful toxins that destroy nearby tissue, generating gas at the same time. A gas composition of 5.9% hydrogen, 3.4% carbon dioxide, 74.5% nitrogen, and 16.1% oxygen was reported in one clinical case.<ref>{{cite journal |vauthors=Chi CH, Chen KW, Huang JJ, Chuang YC, Wu MH |author-link4=Chuang Yin-ching |title=Gas composition in ''Clostridium'' septicum gas gangrene |journal=Journal of the Formosan Medical Association |volume=94 |issue=12 |pages=757–59 |date=December 1995 |pmid=8541740 }}</ref> Gas gangrene is caused by bacterial ]-producing clostridial species, which are mostly found in soil, and other anaerobes such as '']'' and anaerobic ]. These environmental bacteria may enter the muscle through a wound and subsequently proliferate in necrotic tissue and secrete powerful toxins that destroy nearby tissue, generating gas at the same time. A gas composition of 5.9% hydrogen, 3.4% carbon dioxide, 74.5% nitrogen, and 16.1% oxygen was reported in one clinical case.<ref>{{cite journal |vauthors=Chi CH, Chen KW, Huang JJ, Chuang YC, Wu MH |author-link4=Chuang Yin-ching |title=Gas composition in ''Clostridium'' septicum gas gangrene |journal=Journal of the Formosan Medical Association |volume=94 |issue=12 |pages=757–59 |date=December 1995 |pmid=8541740 }}</ref>
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===Other types=== ===Other types===
* ], also known as hemolytic streptococcal gangrene, is a very rare infection that spreads deep into the body along tissue planes. It is characterized by infection with ''S.pyogenes'', a gram-positive cocci bacteria.<ref>{{Cite web|url=https://www.cdc.gov/groupastrep/diseases-hcp/necrotizing-fasciitis.html|title=For Clinicians: Type II Necrotizing Fasciitis {{!}} CDC|date=2019-02-21|website=www.cdc.gov|language=en-us|access-date=2019-08-05}}</ref> * ] is a rare infection that spreads deep into the body along tissue planes. It is categorized into four subtypes, with the first two being the most common. Type 1 requires an infection with an anaerobe and a species in the Enterobacteriaceae family, while type 2 is characterized by infection with '']'', a Gram-positive cocci bacteria, and thus is also known as hemolytic streptococcal gangrene.<ref>{{Cite web|url=https://www.cdc.gov/groupastrep/diseases-hcp/necrotizing-fasciitis.html|title=For Clinicians: Type II Necrotizing Fasciitis |date=2019-02-21|website=www.cdc.gov|language=en-us|access-date=2019-08-05}}</ref><ref>{{cite journal |first1=Rukshini |last1=Puvanendran |first2=Jason |last2=Chan Meng Huey |first3=Shanker |last3=Pasupathy |title=Necrotizing fasciitis |journal=Canadian Family Physician Medecin de Famille Canadien |date=2009 |volume=55 |issue=10 |pages=981–987 |publisher=cfpmfc |pmid=19826154 |pmc=2762295 }}</ref>
* ] is a gangrene of the face common in Africa and Asia, with 99% of cases occurring there, whereas the disease is practically non-existent in other continents.{{citation needed|date=February 2021}} * ] is a gangrene of the face most often found in Africa, Southeast Asia and South America.<ref>{{cite book |last1=Sivapathasundharam |first1=B. |last2=Rajendran |first2=Arya |title=Shafer's Textbook of Oral Pathology |date=30 June 2012 |publisher=Elsevier Health Sciences |isbn=978-81-312-3800-4 |page=333 |url=https://books.google.com/books?id=WnhtAwAAQBAJ&pg=PA333 |language=en}}</ref>
* ] is a type of necrotizing fasciitis that usually affects the genitals and groin.<ref>{{cite journal |last1= Levenson| first1=RB|last2=Singh|first2=AK|last3=Novelline|first3=RA|title=Fournier gangrene: role of imaging |journal=Radiographics |volume= 28 |issue=2 |pages=519–28 |date=March–April 2008 |pmid=18349455|doi=10.1148/rg.282075048 |doi-access=free}}</ref> * ] is a type of necrotizing fasciitis that usually affects the genitals and groin.<ref>{{cite journal |last1= Levenson| first1=RB|last2=Singh|first2=AK|last3=Novelline|first3=RA|title=Fournier gangrene: role of imaging |journal=Radiographics |volume= 28 |issue=2 |pages=519–28 |date=March–April 2008 |pmid=18349455|doi=10.1148/rg.282075048 | s2cid=2930176|doi-access=}}</ref>
* Venous limb gangrene may be caused by ].<ref>{{cite journal |last1=Warkentin|first1=TE|title=Agents for the treatment of heparin-induced thrombocytopenia |journal= Hematology/Oncology Clinics of North America |volume=24 |issue=4 |pages=755–75|date=August 2010 |pmid= 20659659 |doi= 10.1016/j.hoc.2010.05.009 }}</ref> * Venous limb gangrene may be caused by ] and ].<ref>{{cite journal |last1=Warkentin|first1=TE|title=Agents for the treatment of heparin-induced thrombocytopenia |journal= Hematology/Oncology Clinics of North America |volume=24 |issue=4 |pages=755–75|date=August 2010 |pmid= 20659659 |doi= 10.1016/j.hoc.2010.05.009 }}</ref>
* Severe ] may result in gangrene of the ].{{citation needed|date=February 2021}} * Severe ] may result in gangrene of the ].{{citation needed|date=February 2021}}
* Severe ] may result in gangrene of the ].{{citation needed|date=February 2021}} * Severe ] may result in gangrene of the ].{{citation needed|date=February 2021}}
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==History== ==History==
] Private Milton E. Wallen lies in bed with a gangrenous amputated arm]] ] Private Milton E. Wallen lies in bed with a gangrenous amputated arm]]
As early as 1028, ] and ]s were commonly used to treat chronic wounds or ] to prevent or arrest necrotic spread,<ref name="Shi">{{Cite journal | doi=10.12968/bjcn.2014.19.Sup12.S6| pmid=25478859|title = Maggot debridement therapy: A systematic review| journal=British Journal of Community Nursing| volume=19| pages=S6–S13|year = 2014|last1 = Shi|first1 = Eric| last2=Shofler| first2=David}}</ref> as some species of maggots consume only dead flesh, leaving nearby living tissue unaffected. This practice largely died out after the introduction of antibiotics, ],{{Citation needed| date=February 2009}} and ] to the range of treatments for wounds. In recent times, however, ] has regained some credibility and is sometimes employed with great ] in cases of chronic tissue necrosis.<ref>{{cite web |title=Product Classification: Maggots, Medical |url=https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?id=5983 |website= fda.gov| publisher= ]| place= US}}</ref><ref></ref><ref>{{cite journal |pages=32–7 |doi=10.1016/j.ijid.2014.03.1397|pmid=24841930|title=A systematic review of maggot debridement therapy for chronically infected wounds and ulcers|journal= ] |volume= 25| year= 2014| last1= Sun| first1= Xinjuan |last2= Jiang| first2=Kechun|last3=Chen|first3=Jingan|last4=Wu|first4=Liang|last5=Lu|first5=Hui|last6=Wang|first6=Aiping|last7=Wang|first7=Jianming| display-authors= 3| doi-access=free}}</ref> As early as 1028, ] and ]s were commonly used to treat chronic wounds or ] to prevent or arrest necrotic spread,<ref name="Shi">{{Cite journal | doi=10.12968/bjcn.2014.19.Sup12.S6| pmid=25478859|title = Maggot debridement therapy: A systematic review| journal=British Journal of Community Nursing| volume=19| pages=S6–S13|year = 2014|last1 = Shi|first1 = Eric| last2=Shofler| first2=David}}</ref> as some species of maggots consume only dead flesh, leaving nearby living tissue unaffected. This practice largely died out after the introduction of antibiotics to the range of treatments for wounds. In recent times, however, ] has regained some credibility and is sometimes employed with great ] in cases of chronic tissue necrosis.<ref>{{cite web |title=Product Classification: Maggots, Medical |url=https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?id=6212 |website= fda.gov| publisher= ]| place= US}}</ref><ref>{{Cite web|url=http://www.accessdata.fda.gov/cdrh_docs/pdf7/K072438.pdf|title=FDA CDRH 510(k) summary}}</ref><ref>{{cite journal |pages=32–7 |doi=10.1016/j.ijid.2014.03.1397|pmid=24841930|title=A systematic review of maggot debridement therapy for chronically infected wounds and ulcers|journal= ] |volume= 25| year= 2014| last1= Sun| first1= Xinjuan |last2= Jiang| first2=Kechun|last3=Chen|first3=Jingan|last4=Wu|first4=Liang|last5=Lu|first5=Hui|last6=Wang|first6=Aiping|last7=Wang|first7=Jianming| display-authors= 3| doi-access=free}}</ref>


The French ] ] contracted gangrene in January 1687 when, while conducting a performance of his '']'', he stabbed his own toe with his pointed staff (which was used as a ]). The disease spread to his leg, but the composer refused to have his toe ], which eventually led to his death in March of that year.<ref>{{cite web|title=Music Trivia – The Death of Lully|url=http://www.utahsymphony.org/blog/2010/08/music-trivia-the-death-of-lully/|website=The Musician's Lounge|publisher=Utah Symphony Orchestra|access-date=March 7, 2017|date=August 2010}}</ref> The French ] ] contracted gangrene in January 1687 when, while conducting a performance of his '']'', he stabbed his own toe with his pointed staff (which was used as a ]). The disease spread to his leg, but the composer refused to have his toe ], which eventually led to his death in March of that year.<ref>{{cite web|title=Music Trivia – The Death of Lully|url=http://www.utahsymphony.org/blog/2010/08/music-trivia-the-death-of-lully/|website=The Musician's Lounge|publisher=Utah Symphony Orchestra|access-date=March 7, 2017|date=August 2010}}</ref>
Line 105: Line 108:
French King ] died of gangrene in his leg on 1 September 1715, four days prior to his 77th birthday.<ref>{{cite web|last1=Laurenson|first1=John|title=The strange death of Louis XIV|url=http://www.spectator.co.uk/2015/11/the-strange-death-of-louis-xiv/|website=The Spectator|access-date=12 March 2017|date=21 November 2015}}</ref> French King ] died of gangrene in his leg on 1 September 1715, four days prior to his 77th birthday.<ref>{{cite web|last1=Laurenson|first1=John|title=The strange death of Louis XIV|url=http://www.spectator.co.uk/2015/11/the-strange-death-of-louis-xiv/|website=The Spectator|access-date=12 March 2017|date=21 November 2015}}</ref>


], Professor at ], from 1795 on Director of the Medical Bureau of the Batavian Republic, and inspector-general of the French Imperial Military Health-Service in 1811, became a leading expert in the fight against hospital-gangrene and its prevention. He wrote a treatise on gangrene in 1814 in which he meticulously analyzed and explained the causes of this dreadful disease, which he was convinced was contagious. He completed his entry with a thorough evaluation of all possible and well experienced sanitary regulations. His work was very well received and was instrumental in convincing most later authors that gangrene was a contagious disease.<ref>Teun van Heiningen, "Sebald Justinus Brugmans' strijd tegen de hospitaalversterving", Leiden University, URN:NBN:NL:UI:10-1-112565</ref><ref></ref> ], Professor at ], from 1795 on Director of the Medical Bureau of the Batavian Republic, and inspector-general of the French Imperial Military Health-Service in 1811, became a leading expert in the fight against hospital-gangrene and its prevention. He wrote a treatise on gangrene in 1814 in which he meticulously analyzed and explained the causes of this dreadful disease, which he was convinced was contagious. He completed his entry with a thorough evaluation of all possible and well experienced sanitary regulations. His work was very well received and was instrumental in convincing most later authors that gangrene was a contagious disease.<ref>Teun van Heiningen, "Sebald Justinus Brugmans' strijd tegen de hospitaalversterving", Leiden University, URN:NBN:NL:UI:10-1-112565</ref><ref>{{Cite web|url=https://books.google.com/books?id=bliOuPEr9QIC&pg=PA1|title=Verhandeling ter beantwoording der vrage: Kan de gesteldheid en zamenstelling van den dampkring, welke onmiddelijk tot de Hospitaal-versterving (Gangraena NosocomialisZ) aanleiding geeft, door Natuur- of Scheikundige middelen worden ontdekt?|first=Sebald Justinus|last=Brugmans|date=May 24, 1814|publisher=J. van der Heij|via=Google Books}}</ref>


John M. Trombold wrote: "Middleton Goldsmith, a surgeon in the ] during the American Civil War, meticulously studied hospital gangrene and developed a revolutionary treatment regimen. The cumulative Civil War hospital gangrene ] was 45%. Goldsmith's method, which he applied to over 330 cases, yielded a mortality under 3%."<ref>{{cite journal | pmid = 21944621 | volume=77 | issue=9 | title=Gangrene therapy and antisepsis before lister: the civil war contributions of Middleton Goldsmith of Louisville | author=Trombold JM | journal=Am Surg | pages=1138–43 | year=2011| doi=10.1177/000313481107700924 | s2cid=26732207 }}</ref> Goldsmith advocated the use of debridement and topical and injected ] solutions on infected wounds to reduce the incidence and virulence of "poisoned miasma". Copies of his book<ref>. 1863</ref> were issued to Union surgeons to encourage the use of his methods.<ref>{{cite web|last=Watson|first=Dr. Scott|title=Hospital Gangrene During The Civil War – Civil War Medicine|url=http://www.civilwarmedicalbooks.com/hospital_gangrene_civil_war.html|access-date=2014-04-15}}</ref> John M. Trombold wrote: "Middleton Goldsmith, a surgeon in the ] during the American Civil War, meticulously studied hospital gangrene and developed a revolutionary treatment regimen. The cumulative Civil War hospital gangrene ] was 45%. Goldsmith's method, which he applied to over 330 cases, yielded a mortality under 3%."<ref>{{cite journal | pmid = 21944621 | volume=77 | issue=9 | title=Gangrene therapy and antisepsis before lister: the civil war contributions of Middleton Goldsmith of Louisville | author=Trombold JM | journal=Am Surg | pages=1138–43 | year=2011| doi=10.1177/000313481107700924 | s2cid=26732207 | doi-access=free }}</ref> Goldsmith advocated the use of debridement and topical and injected ] solutions on infected wounds to reduce the incidence and virulence of "poisoned miasma". Copies of his book<ref>. 1863</ref> were issued to Union surgeons to encourage the use of his methods.<ref>{{cite web|last=Watson|first=Dr. Scott|title=Hospital Gangrene During The Civil War – Civil War Medicine|url=http://www.civilwarmedicalbooks.com/hospital_gangrene_civil_war.html|access-date=2014-04-15}}</ref>

] also died of gangrene on 17 August 1982.{{cn|date=October 2021}}

== Etymology ==
The ] of gangrene derives from the ] word {{lang|la|gangraena}} and from the ] {{transl|grc|gangraina}} (γάγγραινα), which means "] of tissues".<ref>Liddell & Scott's Lexicon, Oxford University Press, 1963 edition</ref> It has no etymological connection with the word ], despite the affected areas turning black, green, or yellowish brown.{{citation needed|date=February 2021}}


==References== ==References==
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== External links == == External links ==
{{Wiktionary|gangrene|festering}}
* {{Commons category-inline|Gangrene}}

{{Medical condition classification and resources {{Medical condition classification and resources
| DiseasesDB = 19273 | DiseasesDB = 19273
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| MeshID = D005734 | MeshID = D005734
| SNOMED CT = 372070002 | SNOMED CT = 372070002
|ICD11={{ICD11|MC85}}
}} }}
* {{Commons category-inline|Gangrene}}
{{Wiktionary|gangrene|festering}}

{{Ischaemia and infarction}} {{Ischaemia and infarction}}
{{pathology}} {{pathology}}
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] ]
] ]
]
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Latest revision as of 06:39, 26 December 2024

Type of tissue death by infection or lack of blood supply For other uses, see Gangrene (disambiguation). Medical condition
Gangrene
Other namesGangrenous necrosis
Dry gangrene affecting the toes as a result of peripheral artery disease
SpecialtyInfectious disease, surgery, podiatry
SymptomsChange in skin color to red or black, numbness, pain, skin breakdown, coolness
ComplicationsSepsis, amputation
TypesDry, wet, gas, internal, necrotizing fasciitis
Risk factorsDiabetes, peripheral arterial disease, smoking, major trauma, alcoholism, plague, HIV/AIDS, frostbite, Raynaud's syndrome
Diagnostic methodBased on symptom, With medical imaging used to identify the underlying cause.
TreatmentDepends on underlying cause
PrognosisVariable
FrequencyUnknown
Gangrene toes in a diabetic

Gangrene is a type of tissue death caused by a lack of blood supply. Symptoms may include a change in skin color to red or black, numbness, swelling, pain, skin breakdown, and coolness. The feet and hands are most commonly affected. If the gangrene is caused by an infectious agent, it may present with a fever or sepsis.

Risk factors include diabetes, peripheral arterial disease, smoking, major trauma, alcoholism, HIV/AIDS, frostbite, influenza, dengue fever, malaria, chickenpox, plague, hypernatremia, radiation injuries, meningococcal disease, Group B streptococcal infection and Raynaud's syndrome. It can be classified as dry gangrene, wet gangrene, gas gangrene, internal gangrene, and necrotizing fasciitis. The diagnosis of gangrene is based on symptoms and supported by tests such as medical imaging.

Treatment may involve surgery to remove the dead tissue, antibiotics to treat any infection, and efforts to address the underlying cause. Surgical efforts may include debridement, amputation, or the use of maggot therapy. Efforts to treat the underlying cause may include bypass surgery or angioplasty. In certain cases, hyperbaric oxygen therapy may be useful. How commonly the condition occurs is unknown.

Etymology

The etymology of gangrene derives from the Latin word gangraena and from the Greek gangraina (γάγγραινα), which means "putrefaction of tissues".

Signs and symptoms

Four drawn illustrations on a page, including (top left) a foot with black toes, (top right) a limb with holes in the skin showing yellowed matter beneath, (centre right) the end of a foot with blackened stubs where the toes once were, and (bottom) a foot that is wrinkled and dark, with prominent veins and purple toes.
An illustration showing four different stages of gangrene, including one (Fig. 4 top right) caused by an obstacle to the return of the venous blood due to heart disease.

Symptoms may include a change in skin color to red or black, numbness, pain, skin breakdown, and coolness. The feet and hands are most commonly involved.

Causes

Gangrene is caused by a critically insufficient blood supply (e.g., peripheral vascular disease) or infection. It is associated with diabetes and long-term tobacco smoking.

Dry gangrene

Dry gangrene is a form of coagulative necrosis that develops in ischemic tissue, where the blood supply is inadequate to keep tissue viable. It is not a disease itself, but a symptom of other diseases. The term dry is used only when referring to a limb or to the gut (in other locations, this same type of necrosis is called an infarction, such as myocardial infarction). Dry gangrene is often due to peripheral artery disease, but can be due to acute limb ischemia. As a result, people with atherosclerosis, high cholesterol, diabetes and smokers commonly have dry gangrene. The limited oxygen in the ischemic limb limits putrefaction and bacteria fail to survive. The affected part is dry, shrunken, and dark reddish-black. The line of separation usually brings about complete separation, with eventual falling off of the gangrenous tissue if it is not removed surgically, a process called autoamputation.

Dry gangrene is the result of chronic ischemia without infection. If ischemia is detected early, when ischemic wounds rather than gangrene are present, the process can be treated by revascularization (via vascular bypass or angioplasty). However, once gangrene has developed, the affected tissues are not salvageable. Because dry gangrene is not accompanied by infection, it is not as emergent as gas gangrene or wet gangrene, both of which have a risk of sepsis. Over time, dry gangrene may develop into wet gangrene if an infection develops in the dead tissues.

Diabetes mellitus is a risk factor for peripheral vascular disease, thus for dry gangrene, but also a risk factor for wet gangrene, particularly in patients with poorly controlled blood sugar levels, as elevated serum glucose creates a favorable environment for bacterial infection.

Wet gangrene

Wet gangrene of the foot.

Wet, or infected, gangrene is characterized by thriving bacteria and has a poor prognosis (compared to dry gangrene) due to sepsis resulting from the free communication between infected fluid and circulatory fluid. In wet gangrene, the tissue is infected by saprogenic microorganisms (Clostridium perfringens or Bacillus fusiformis, for example), which cause tissue to swell and emit a foul odor. Wet gangrene usually develops rapidly due to blockage of venous (mainly) or arterial blood flow. The affected part is saturated with stagnant blood, which promotes the rapid growth of bacteria. The toxic products formed by bacteria are absorbed, causing systemic manifestation of sepsis and finally death. The affected part is edematous, soft, putrid, rotten, and dark.

Because of the high mortality associated with infected gangrene (about 80% without treatment and 20% with treatment), an emergency salvage amputation, such as a guillotine amputation, is often needed to limit systemic effects of the infection. Such an amputation can be converted to a formal amputation, such as a below- or above-knee amputation.

Gas gangrene

Main article: Gas gangrene

Gas gangrene is a bacterial infection that produces gas within tissues. It can be caused by Clostridium, most commonly alpha toxin-producing C. perfringens, or various nonclostridial species. Infection spreads rapidly as the gases produced by the bacteria expand and infiltrate healthy tissue in the vicinity. Because of its ability to quickly spread to surrounding tissues, gas gangrene should be treated as a medical emergency.

Gas gangrene is caused by bacterial exotoxin-producing clostridial species, which are mostly found in soil, and other anaerobes such as Bacteroides and anaerobic streptococci. These environmental bacteria may enter the muscle through a wound and subsequently proliferate in necrotic tissue and secrete powerful toxins that destroy nearby tissue, generating gas at the same time. A gas composition of 5.9% hydrogen, 3.4% carbon dioxide, 74.5% nitrogen, and 16.1% oxygen was reported in one clinical case.

Gas gangrene can cause necrosis, gas production, and sepsis. Progression to toxemia and shock is often very rapid.

Other types

  • Necrotizing fasciitis is a rare infection that spreads deep into the body along tissue planes. It is categorized into four subtypes, with the first two being the most common. Type 1 requires an infection with an anaerobe and a species in the Enterobacteriaceae family, while type 2 is characterized by infection with Streptococcus pyogenes, a Gram-positive cocci bacteria, and thus is also known as hemolytic streptococcal gangrene.
  • Noma is a gangrene of the face most often found in Africa, Southeast Asia and South America.
  • Fournier gangrene is a type of necrotizing fasciitis that usually affects the genitals and groin.
  • Venous limb gangrene may be caused by Heparin-induced thrombocytopenia and thrombosis.
  • Severe mesenteric ischemia may result in gangrene of the small intestine.
  • Severe ischemic colitis may result in gangrene of the large intestine.

Treatment

Treatment varies based on the severity and type of gangrene.

Lifestyle

Exercises such as walking and massage therapy may be tried.

Medication

Medications may include pain management, medications that promote circulation in the circulatory system and antibiotics. Since gangrene is associated with periodic pain caused by too little blood flow, pain management is important so patients can continue doing exercises that promote circulation. Pain management medications can include opioids and opioid-like analgesics. Since gangrene is a result of ischemia, circulatory system management is important. These medications can include antiplatelet drug, anticoagulant, and fibrinolytics. As infection is often associated with gangrene, antibiotics are often a critical component of its treatment. The life-threatening nature of gangrene requires treatment with intravenous antibiotics in an inpatient setting. Antibiotics alone are not effective because they may not penetrate infected tissues sufficiently.

Surgery

Surgical removal of all dead tissue, however, is the mainstay of treatment for gangrene. Often, gangrene is associated with underlying infection, thus the gangrenous tissue must be debrided to hinder the spread of the associated infection. The extent of surgical debridement needed depends on the extent of the gangrene and may be limited to the removal of a finger, toe, or ear, but in severe cases may involve a limb amputation.

Dead tissue alone does not require debridement, and in some cases, such as dry gangrene, the affected part falls off (autoamputates), making surgical removal unnecessary. Waiting for autoamputation, however, may cause health complications as well as decreased quality of life.

After the gangrene is treated with debridement and antibiotics, the underlying cause can be treated. In the case of gangrene due to critical limb ischemia, revascularization can be performed to treat the underlying peripheral underlateral artery disease.

Ischemic disease of the legs is the most common reason for amputations. In about a quarter of these cases, the other side requires amputation in the next three years.

Angioplasty should be considered if severe blockage in lower leg vessels (tibial and peroneal artery) leads to gangrene.

Other

Hyperbaric oxygen therapy treatment is used to treat gas gangrene. It increases pressure and oxygen content to allow blood to carry more oxygen to inhibit anaerobic organism growth and reproduction.

Regenerative medical treatments and stem-cell therapies have successfully altered gangrene and ulcer prognosis.

History

Union Army Private Milton E. Wallen lies in bed with a gangrenous amputated arm

As early as 1028, flies and maggots were commonly used to treat chronic wounds or ulcers to prevent or arrest necrotic spread, as some species of maggots consume only dead flesh, leaving nearby living tissue unaffected. This practice largely died out after the introduction of antibiotics to the range of treatments for wounds. In recent times, however, maggot therapy has regained some credibility and is sometimes employed with great efficacy in cases of chronic tissue necrosis.

The French Baroque composer Jean-Baptiste Lully contracted gangrene in January 1687 when, while conducting a performance of his Te Deum, he stabbed his own toe with his pointed staff (which was used as a baton). The disease spread to his leg, but the composer refused to have his toe amputated, which eventually led to his death in March of that year.

French King Louis XIV died of gangrene in his leg on 1 September 1715, four days prior to his 77th birthday.

Sebald Justinus Brugmans, Professor at Leyden University, from 1795 on Director of the Medical Bureau of the Batavian Republic, and inspector-general of the French Imperial Military Health-Service in 1811, became a leading expert in the fight against hospital-gangrene and its prevention. He wrote a treatise on gangrene in 1814 in which he meticulously analyzed and explained the causes of this dreadful disease, which he was convinced was contagious. He completed his entry with a thorough evaluation of all possible and well experienced sanitary regulations. His work was very well received and was instrumental in convincing most later authors that gangrene was a contagious disease.

John M. Trombold wrote: "Middleton Goldsmith, a surgeon in the Union Army during the American Civil War, meticulously studied hospital gangrene and developed a revolutionary treatment regimen. The cumulative Civil War hospital gangrene mortality was 45%. Goldsmith's method, which he applied to over 330 cases, yielded a mortality under 3%." Goldsmith advocated the use of debridement and topical and injected bromide solutions on infected wounds to reduce the incidence and virulence of "poisoned miasma". Copies of his book were issued to Union surgeons to encourage the use of his methods.

References

  1. ^ "Gangrene Symptoms". NHS. 13 October 2015. Retrieved 12 December 2017.
  2. ^ "Gangrene". patient.info. 12 March 2014. Retrieved 12 December 2017.
  3. ^ "Gangrene Causes". NHS. 13 October 2015. Retrieved 12 December 2017.
  4. ^ "Gangrene". NHS. 13 October 2015. Retrieved 12 December 2017.
  5. ^ "Gangrene Treatment". NHS. Retrieved 12 December 2017.
  6. "Gangrene Diagnosis". NHS. 13 October 2015. Retrieved 12 December 2017.
  7. Liddell & Scott's Lexicon, Oxford University Press, 1963 edition
  8. Gardner, AW; Afaq, A (November–December 2008). "Management of lower extremity peripheral arterial disease". Journal of Cardiopulmonary Rehabilitation and Prevention. 28 (6): 349–57. doi:10.1097/HCR.0b013e31818c3b96. PMC 2743684. PMID 19008688.
  9. ^ Yang, Z; Hu, J; Qu, Y; Sun, F; Leng, X; Li, H; Zhan, S (3 December 2015). "Interventions for treating gas gangrene". The Cochrane Database of Systematic Reviews. 2015 (12): CD010577. doi:10.1002/14651858.CD010577.pub2. PMC 8652263. PMID 26631369.
  10. Korzon-Burakowska, A; Dziemidok, P (December 2011). "Diabetic foot-the need for comprehensive multidisciplinary approach". Annals of Agricultural and Environmental Medicine. 18 (2): 314–17. PMID 22216805.
  11. Smith, Tyler (2015). Gangrene Management: Today and Tomorrow. Hayle Medical. ISBN 978-1632412232.
  12. Cross, Simon (2018). Underwood's Pathology: A Clinical Approach (7th ed.). Elsevier Health Sciences. p. 124. ISBN 9780702072109. Retrieved 8 April 2020.
  13. ^ Al Wahbi, Abdullah (2018-06-01). "Autoamputation of diabetic toe with dry gangrene: a myth or a fact?". Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy. 11: 255–264. doi:10.2147/DMSO.S164199. ISSN 1178-7007. PMC 5987754. PMID 29910628.
  14. Aiello A, Anichini R, Brocco E, Caravaggi C, Chiavetta A, Cioni R, Da Ros R, De Feo ME, Ferraresi R, Florio F, Gargiulo M, Galzerano G, Gandini R, Giurato L, Graziani L, Mancini L, Manzi M, Modugno P, Setacci C, Uccioli L (2014). "Treatment of peripheral arterial disease in diabetes: a consensus of the Italian Societies of Diabetes (SID, AMD), Radiology (SIRM) and Vascular Endovascular Surgery (SICVE)". Nutr Metab Cardiovasc Dis. 24 (4): 355–69. doi:10.1016/j.numecd.2013.12.007. PMID 24486336.
  15. Gerhard-Herman, MD; Gornik, HL; Barrett, C; Barshes, NR; Corriere, MA; Drachman, DE; Fleisher, LA; Fowkes, FG; Hamburg, NM; Kinlay, S; Lookstein, R; Misra, S; Mureebe, L; Olin, JW; Patel, RA; Regensteiner, JG; Schanzer, A; Shishehbor, MH; Stewart, KJ; Treat-Jacobson, D; Walsh, ME (2017). "2016 AHA/ACC Guideline on the Management of Patients With Lower Extremity Peripheral Artery Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines". Circulation. 135 (12): e726–79. doi:10.1161/CIR.0000000000000471. PMC 5477786. PMID 27840333.
  16. Nather, Aziz (2013). The diabetic foot. World Scientific. ISBN 978-9814417006.
  17. Vayvada, H; Demirdover, C; Menderes, A; Karaca, C (August 2013). "Necrotising fasciitis in the central part of the body: diagnosis, management and review of the literature". International Wound Journal. 10 (4): 466–72. doi:10.1111/j.1742-481x.2012.01006.x. PMC 7950796. PMID 22694053. S2CID 5693425.
  18. ^ Tisi, PV; Than, MM (8 April 2014). "Type of incision for below knee amputation". The Cochrane Database of Systematic Reviews. 2014 (4): CD003749. doi:10.1002/14651858.CD003749.pub3. PMC 7154343. PMID 24715679.
  19. Sakurai, J.; Nagahama, M.; Oda, M. (November 2004). "Clostridium perfringens alpha-toxin: characterization and mode of action". Journal of Biochemistry. 136 (5): 569–74. doi:10.1093/jb/mvh161. PMID 15632295. S2CID 12940936.
  20. Chi CH, Chen KW, Huang JJ, Chuang YC, Wu MH (December 1995). "Gas composition in Clostridium septicum gas gangrene". Journal of the Formosan Medical Association. 94 (12): 757–59. PMID 8541740.
  21. "Gas Gangrene". The Lecturio Medical Concept Library. Retrieved 22 July 2021.
  22. "For Clinicians: Type II Necrotizing Fasciitis". www.cdc.gov. 2019-02-21. Retrieved 2019-08-05.
  23. Puvanendran, Rukshini; Chan Meng Huey, Jason; Pasupathy, Shanker (2009). "Necrotizing fasciitis". Canadian Family Physician Medecin de Famille Canadien. 55 (10). cfpmfc: 981–987. PMC 2762295. PMID 19826154.
  24. Sivapathasundharam, B.; Rajendran, Arya (30 June 2012). Shafer's Textbook of Oral Pathology. Elsevier Health Sciences. p. 333. ISBN 978-81-312-3800-4.
  25. Levenson, RB; Singh, AK; Novelline, RA (March–April 2008). "Fournier gangrene: role of imaging". Radiographics. 28 (2): 519–28. doi:10.1148/rg.282075048. PMID 18349455. S2CID 2930176.
  26. Warkentin, TE (August 2010). "Agents for the treatment of heparin-induced thrombocytopenia". Hematology/Oncology Clinics of North America. 24 (4): 755–75. doi:10.1016/j.hoc.2010.05.009. PMID 20659659.
  27. Lipsky BA (December 1999). "Evidence-based antibiotic therapy of diabetic foot infections". FEMS Immunol. Med. Microbiol. 26 (3–4): 267–76. doi:10.1016/s0928-8244(99)00143-1. PMID 10575138.
  28. Amputations of the Lower Extremity at eMedicine
  29. "Angioplasty and stent placement – peripheral arteries". Retrieved July 24, 2013.
  30. Liu R, Li L, Yang M, Boden G, Yang G (2013). "Systematic review of the effectiveness of hyperbaric oxygenation therapy in the management of chronic diabetic foot ulcers". Mayo Clin. Proc. 88 (2): 166–75. doi:10.1016/j.mayocp.2012.10.021. PMID 23374620.
  31. Shi, Eric; Shofler, David (2014). "Maggot debridement therapy: A systematic review". British Journal of Community Nursing. 19: S6 – S13. doi:10.12968/bjcn.2014.19.Sup12.S6. PMID 25478859.
  32. "Product Classification: Maggots, Medical". fda.gov. US: Food and Drug Administration.
  33. "FDA CDRH 510(k) summary" (PDF).
  34. Sun, Xinjuan; Jiang, Kechun; Chen, Jingan; et al. (2014). "A systematic review of maggot debridement therapy for chronically infected wounds and ulcers". International Journal of Infectious Diseases. 25: 32–7. doi:10.1016/j.ijid.2014.03.1397. PMID 24841930.
  35. "Music Trivia – The Death of Lully". The Musician's Lounge. Utah Symphony Orchestra. August 2010. Retrieved March 7, 2017.
  36. Laurenson, John (21 November 2015). "The strange death of Louis XIV". The Spectator. Retrieved 12 March 2017.
  37. Teun van Heiningen, "Sebald Justinus Brugmans' strijd tegen de hospitaalversterving", Leiden University, URN:NBN:NL:UI:10-1-112565
  38. Brugmans, Sebald Justinus (May 24, 1814). "Verhandeling ter beantwoording der vrage: Kan de gesteldheid en zamenstelling van den dampkring, welke onmiddelijk tot de Hospitaal-versterving (Gangraena NosocomialisZ) aanleiding geeft, door Natuur- of Scheikundige middelen worden ontdekt?". J. van der Heij – via Google Books.
  39. Trombold JM (2011). "Gangrene therapy and antisepsis before lister: the civil war contributions of Middleton Goldsmith of Louisville". Am Surg. 77 (9): 1138–43. doi:10.1177/000313481107700924. PMID 21944621. S2CID 26732207.
  40. A report on hospital gangrene, erysipelas and pyaemia. 1863
  41. Watson, Dr. Scott. "Hospital Gangrene During The Civil War – Civil War Medicine". Retrieved 2014-04-15.

External links

  • Media related to Gangrene at Wikimedia Commons
ClassificationD
External resources
Ischaemia and infarction
Ischemia
Infarction
Pathology
Principles of pathology
Cellular adaptation
Atrophy
Hypertrophy
Hyperplasia
Dysplasia
Metaplasia
Squamous
Glandular
Cell death
Necrosis
Coagulative necrosis
Liquefactive necrosis
Gangrenous necrosis
Caseous necrosis
Fat necrosis
Fibrinoid necrosis
Myocytolysis
Programmed cell death
Apoptosis
Pyknosis
Karyorrhexis
Karyolysis
Accumulations
pigment
Hemosiderin
Lipochrome/Lipofuscin
Melanin
Steatosis
Anatomical pathology
Clinical pathology
Bacterial skin disease
Gram +ve
Bacillota
Staphylococcus
Streptococcus
CorynebacteriumErythrasma
Clostridium
Others
Actinomycetota
Mycobacterium-
related
Others
Gram -ve
Pseudomonadota
Alpha
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Gamma
Campylobacterota
Other
Unspecified
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