Granulomatous pigmented purpuric dermatosis: report of a Latin-American case with blaschkoid distribution.

Abstract:

:Granulomatous pigmented purpuric dermatosis clinically manifests as hyperpigmented maculae and petechiae, predominantly on the lower extremities. Histopathologically, it is characterized by a lymphocytic infiltrate in the upper dermis, extravasated erythrocytes, and hemosiderin deposits. There is an infrequent variant called granulomatous pigmented purpuric dermatosis, which histologically is characterized by the presence of non-necrotizing granulomas associated with the classic findings of other pigmented purpuric dermatoses. It more frequently affects middle-aged women of Asian origin, and predominantly on the lower extremities. The authors present the case of a female patient with granulomatous pigmented purpuric dermatosis on the lower extremities with blaschkoid distribution.

journal_name

An Bras Dermatol

authors

Carvajal D,Quiroz C,Morales C,Fernández J

doi

10.1016/j.abd.2019.09.002

subject

Has Abstract

pub_date

2019-01-01 00:00:00

pages

582-585

issue

5

eissn

0365-0596

issn

1806-4841

pii

S0365-0596(19)30033-9

journal_volume

94

pub_type

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