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 Dermatoljournal_title
Anais brasileiros de dermatologiaauthors
Carvajal D,Quiroz C,Morales C,Fernández Jdoi
10.1016/j.abd.2019.09.002subject
Has Abstractpub_date
2019-01-01 00:00:00pages
582-585issue
5eissn
0365-0596issn
1806-4841pii
S0365-0596(19)30033-9journal_volume
94pub_type
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