Doucas and Kapetanakis pigmented purpura

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]

See also

References

  1. ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0. 
  2. ^ Wolfram Sterry; Ralf Paus; Walter H. C. Burgdorf (8 March 2006). Dermatology. Thieme. pp. 246–. ISBN 9781588902580. http://books.google.com/books?id=c2IJFZqWtmwC&pg=PA246. Retrieved 22 May 2010. 
  3. ^ 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 9780781768450. http://books.google.com/books?id=-uqJzY08OqUC&pg=PA127. Retrieved 22 May 2010. 
  4. ^ DOUCAS C, KAPETANAKIS J (1953). "Eczematid-like purpura". Dermatologica 106 (2): 86–95. PMID 13060054. 
Hyper-
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
Other/ungrouped
Acanthosis nigricans (Acral acanthotic anomaly) · 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
Dyschromatoses
Dyschromatosis symmetrica hereditaria · Dyschromatosis universalis hereditaria

M: INT, SF, LCT

anat/phys/devp

noco(i/b/d/q/u/r/p/m/k/v/f)/cong/tumr(n/e/d), sysi/epon

proc, drug (D2/3/4/5/8/11)

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