KMID : 0032220110230040508
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Annals of Dermatology 2011 Volume.23 No. 4 p.508 ~ p.511
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Benign Cephalic Histiocytosis: A Case Report
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Koca Rafet
Bektas Sibel Altinyazar H. Cevdet Sezer Tuna
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Abstract
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Histiocytic skin disorders are usually classified as either Langerhans¡¯ cell histiocytosis (LCH) or non LCH, based on the pathology. Benign cephalic histiocytosis (BCH) is a rare type of non-Langerhans histiocytitic disorder and is characterized by self-healing multiple small eruptions of yellow to red-brown papules on the face and upper trunk. Histologic features of this disorder show dermal proliferation of histiocytes that have intracytoplasmic comma-shaped bodies, coated vesicles and desmosome-like structures. In this study, we report on a 7-month-old boy who contained small yellow-red papules on his face that spread to his upper trunk. The clinical and histologic features in this patient were consistent with BCH.
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KEYWORD
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Benign cephalic histiocytosis, Generalized eruptive histiocytoma, Infant, Juvenile xanthogranuloma, Non-Langerhans- Cell
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