Benign Cephalic Histiocytosis: A Case Report
Küçük Resim Yok
Tarih
2011
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
KOREAN DERMATOLOGICAL ASSOC
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
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. (Ann Dermatol 23(4) 508 similar to 511, 2011)
Açıklama
Anahtar Kelimeler
Benign cephalic histiocytosis, Generalized eruptive histiocytoma, Infant, juvenile xanthogranuloma, Non-Langerhans-Cell
Kaynak
ANNALS OF DERMATOLOGY
WoS Q Değeri
Q4
Scopus Q Değeri
Q3
Cilt
23
Sayı
4
