Claudy A L, Misery L, Serre D, Boucheron S
Department of Dermatology, University Hospital, Hôpital Nord, St Priest en Jarez, France.
Pediatr Dermatol. 1993 Mar;10(1):61-3. doi: 10.1111/j.1525-1470.1993.tb00017.x.
A 4-month-old boy had numerous nodular lesions. Microscopic findings revealed a histiocytic proliferation without foam cells and giant cells. Immunohistochemical studies showed that the histiocytes belonged to the monocyte-macrophage system and not to the Langerhans cell system. This case is an unusual variant of juvenile xanthogranuloma that, when congenital, may be difficult to differentiate from Hashimoto-Pritzker disease.
一名4个月大的男婴有许多结节性病变。显微镜检查结果显示为组织细胞增殖，无泡沫细胞和巨细胞。免疫组织化学研究表明，这些组织细胞属于单核巨噬细胞系统，而非朗格汉斯细胞系统。该病例是幼年黄色肉芽肿的一种不寻常变体，先天性时可能难以与桥本-普里茨克病相鉴别。
