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Acral pseudolymphomatous angiokeratoma of children (APACHE)
Author(s) -
Kim Youngjin,
DawesHiggs Elizabeth,
Mann Stephen,
Cook David K
Publication year - 2005
Publication title -
australasian journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.67
H-Index - 53
eISSN - 1440-0960
pISSN - 0004-8380
DOI - 10.1111/j.1440-0960.2005.00174.x
Subject(s) - medicine , angiokeratoma , dermatology , histopathology , lesion , hyperplasia , pathology
SUMMARY A 13‐year‐old girl presented with a 10‐year history of multiple discrete red firm papules situated on her right upper arm. The histopathology examination revealed a massive subepidermal lymphohistiocytic infiltrate, consistent with acral pseudolymphomatous angiokeratoma of children. Treatment with topical application of mometasone furoate 0.1% cream once daily for 6 months improved the lesions partially. However, these papules returned to their pretreatment appearance and consistency within 6 months after the cessation of the topical corticosteroid. The authors prefer the term ‘papular angiolymphoid hyperplasia’ for this entity, based on the absence of histological angiokeratomatous features, the benign nature of the lesion and the previously reported cases from adults and non‐acral sites.