Mishkel M A, Cockshott W P, Nazir D J, Rosenthal D, Spaulding W P, Wynn-Williams A
Arch Dermatol. 1977 Aug;113(8):1094-1100. doi: 10.1001/archderm.113.8.1094.
A 55-year-old man with the classical mucocutaneous lesions of xanthoma disseminatum has been followed up for a period of 13 years. The special features of this case, which make it unique, are as follows: (1) the availability of histologic data on multiple lesions for more than a ten-year period; (2) the progressive nature of the multiple osseous lesions; (3) the metabolic studies that show no evidence for accumulation of abnormal sterols in a xanthoma, the blood, or intestinal aspirate; (4) the development of hypothyroidism and symptoms or signs, or both, of an intracerebral and an intraspinal lesion; (5) the partial regression of the cutanous symptoms and lesions while receiving clofibrate, in spite of progression of the mucous membrane and osseous lesions, and (6) the failure to develop diabetes insipidus to date.
一名患有播散性黄瘤典型黏膜皮肤损害的55岁男性已被随访13年。该病例的特殊之处使其独一无二,具体如下:(1)有超过十年的多个病变的组织学数据;(2)多个骨病变的进行性特点;(3)代谢研究表明在黄瘤、血液或肠道吸出物中没有异常固醇积累的证据;(4)出现甲状腺功能减退以及脑内和脊髓内病变的症状或体征,或两者皆有;(5)尽管黏膜和骨病变进展,但在接受氯贝丁酯治疗时皮肤症状和病变部分消退;(6)迄今为止未发生尿崩症。