Doucas and Kapetanakis pigmented purpura

Doucas and Kapetanakis pigmented purpura
Classification and external resources
DiseasesDB	30753

Doucas and Kapetanakis pigmented purpura is a skin condition characterized by scaly and eczematous patches, which also have petechiae and hemosiderin staining.^[1]^:830

It is also known as "eczematoid purpura"^[2] or "eczematoid-like purpura".^[3]

It was characterized in 1953.^[4]

References

↑ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.
↑ 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.
↑ C. Doucas and J Kapetanakis (1953). "Eczematid-like purpura". Dermatologica 106 (2): 86–95. doi:10.1159/000256830. PMID 13060054.

Pigmentation disorders/Dyschromia (L80–L81, 709.0)

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

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 Tattoo Tar melanosis

Dyschromatoses

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Doucas and Kapetanakis pigmented purpura

See also

References