Journal
PEDIATRIC DERMATOLOGY
Volume 24, Issue 5, Pages 517-524Publisher
BLACKWELL PUBLISHING
DOI: 10.1111/j.1525-1470.2007.00508.x
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Funding
- NCI NIH HHS [T32-CA 09,140] Funding Source: Medline
- NIAMS NIH HHS [T32-AR 007,442] Funding Source: Medline
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Skin findings in childhood sarcoidosis vary greatly, but only a few occurrences have been published in which the histopathology has been characterized well. We describe a child with sarcoidosis in whom the cutaneous findings were atypical, resembling granuloma annulare. Histologic examination of these cutaneous lesions, however, revealed areas of sarcoid-like epithelioid cell granulomas, a palisading granulomatous process with features of granuloma annulare, as well as palisading neutrophilic and granulornatous dermatitis and interstitial granulornatous dermatitis. This underscores the variability of skin findings in childhood sarcoldosis-even within the same patient-and suggests that sarcoidosis should be considered in the differential diagnosis of children initially diagnosed with granulomatous skin lesions, such as granuloma annulare, palisading neutrophilic, and granulomatous dermatitis or interstitial granulornatous dermatitis, who demonstrate associated signs of systemic disease.
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