Biess B, Gartmann H
Z Hautkr. 1985 Jan;60(1-2):219-28.
We report on a 19-year-old girl suffering from cutaneous manifestation of sinus histiocytosis associated with massive lymphadenopathy (SHML) (Rosai-Dorfman syndrome); as SHML had first appeared at her 7th month of life, the disease had taken an uncommonly long period of time. At the age of 15, cutaneous manifestations developed on cheeks and left upper arm which histologically showed the same infiltrate as affected lymph nodes usually do in SHML. So far, participation of the cutaneous system in SHML has been observed in only 12 cases.
我们报告了一名19岁女孩，患有伴有巨大淋巴结病的窦性组织细胞增生症（SHML）（罗萨伊-多夫曼综合征）的皮肤表现；由于SHML在她7个月大时首次出现，病程持续了异常长的时间。15岁时，脸颊和左上臂出现皮肤表现，组织学检查显示与SHML中受影响淋巴结通常所见的浸润相同。迄今为止，仅在12例病例中观察到皮肤系统参与SHML。
