Doucas and Kapetanakis pigmented purpura

(Redirected from Eczematid-like purpura of Doucas and Kapetanakis) Medical condition

Doucas and Kapetanakis pigmented purpura
Other names	Eczematoid purpura, eczematoid-like purpura.
Specialty	Dermatology

Doucas and Kapetanakis pigmented purpura, also known as eczematoid purpura, or eczematoid-like purpura, is a skin condition characterized by scaly and eczematous patches, which also have petechiae and hemosiderin staining.

It is a lymphocytic capillaritis of unknown cause. Lesions consist of erythematous and purpuric macules which usually begin around the ankles, coalesce, and spread to involve the whole legs, and sometimes the trunk and upper extremities. The lesions are extremely pruritic (itchy) and occasionally lichenified after prolonged scratching.

It was characterized in 1953.

References

Wolfram Sterry; Ralf Paus; Walter H. C. Burgdorf (8 March 2006). Dermatology. Thieme. pp. 246–. ISBN 978-1-58890-258-0. Retrieved 22 May 2010.
David E. Elder; Rosalie Elenitsas; Michael D. Ioffreda; Bernett L. Johnson Jr. (2007). Atlas and synopsis of Lever's histopathology of the skin. Lippincott Williams & Wilkins. pp. 127–. ISBN 978-0-7817-6845-0. Retrieved 22 May 2010.
James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.
C. Doucas; J Kapetanakis (1953). "Eczematid-like purpura". Dermatologica. 106 (2): 86–95. doi:10.1159/000256830. PMID 13060054.

External links

Classification	D DiseasesDB: 30753

Pigmentation disorders/Dyschromia

Hypo-/
leucism

Loss of
melanocytes

Vitiligo	Quadrichrome vitiligo Vitiligo ponctué
Syndromic	Alezzandrini syndrome Vogt–Koyanagi–Harada syndrome
Melanocyte development	Piebaldism Waardenburg syndrome Tietz syndrome

Loss of melanin/
amelanism

Albinism	Oculocutaneous albinism Ocular albinism in humans
Melanosome transfer	Hermansky–Pudlak syndrome Chédiak–Higashi syndrome Griscelli syndrome Elejalde syndrome Griscelli syndrome type 2 Griscelli syndrome type 3
Other	Cross syndrome ABCD syndrome Albinism–deafness syndrome Idiopathic guttate hypomelanosis Phylloid hypomelanosis Progressive macular hypomelanosis

Leukoderma w/o
hypomelanosis

Ungrouped

Hyper-

Melanin/
Melanosis/
Melanism

Reticulated	Dermatopathia pigmentosa reticularis Pigmentatio reticularis faciei et colli Reticulate acropigmentation of Kitamura Reticular pigmented anomaly of the flexures Naegeli–Franceschetti–Jadassohn syndrome Dyskeratosis congenita X-linked reticulate pigmentary disorder Galli–Galli disease Revesz syndrome
Diffuse/ circumscribed	Lentigo/Lentiginosis: Lentigo simplex Liver spot Centrofacial lentiginosis Generalized lentiginosis Inherited patterned lentiginosis in black persons Ink spot lentigo Lentigo maligna Mucosal lentigines Partial unilateral lentiginosis PUVA lentigines Melasma Erythema dyschromicum perstans Lichen planus pigmentosus Café au lait spot Poikiloderma (Poikiloderma of Civatte Poikiloderma vasculare atrophicans) Riehl melanosis
Linear	Incontinentia pigmenti Scratch dermatitis Shiitake mushroom dermatitis
Other/ ungrouped	Acanthosis nigricans Freckle Familial progressive hyperpigmentation Pallister–Killian syndrome Periorbital hyperpigmentation Photoleukomelanodermatitis of Kobori Postinflammatory hyperpigmentation Transient neonatal pustular melanosis

Other
pigments

Iron	Hemochromatosis Iron metallic discoloration Pigmented purpuric dermatosis Schamberg disease Majocchi's disease Gougerot–Blum syndrome Doucas and Kapetanakis pigmented purpura/Eczematid-like purpura of Doucas and Kapetanakis Lichen aureus Angioma serpiginosum Hemosiderin hyperpigmentation
Other metals	Argyria Chrysiasis Arsenic poisoning Lead poisoning Titanium metallic discoloration
Other	Carotenosis Tar melanosis

Dyschromia

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