Forrest E, Gallacher S J, Hadley D, Soukop M, Boyle I T
University Department of Medicine, Glasgow Royal Infirmary.
Scott Med J. 1993 Oct;38(5):148-9. doi: 10.1177/003693309303800507.
Histiocytosis X is the term first coined by Lichtenstein in 1953 to describe a heterogeneous group of disorders which is considered now to include Hand-Schuller-Christian disease, Letterer-Siwe disease and Eosinophilic Granuloma of bone. Gagel, in 1941, first described involvement of the central nervous system (CNS) in Histiocytosis X--in this case the hypothalamus and posterior pituitary were the areas principally affected. CNS involvement outwith these areas is rare, generally difficult to diagnose, and little information on treatment is available. In this case we describe a man with cranial histiocytosis X who was treated with intrathecal and systemic chemotherapy and cranial irradiation, and we comment upon the value of magnetic resonance imaging (MRI) in this condition.
组织细胞增多症X是1953年利希滕斯坦首次提出的术语,用于描述一组异质性疾病,现在认为包括汉-许-克病、勒-雪病和骨嗜酸性肉芽肿。1941年,加格尔首次描述了组织细胞增多症X累及中枢神经系统(CNS)的情况——在该病例中,下丘脑和垂体后叶是主要受累部位。中枢神经系统在这些区域之外的受累情况罕见,通常难以诊断,且关于治疗的信息很少。在本病例中,我们描述了一名患有颅骨组织细胞增多症X的男性患者,他接受了鞘内和全身化疗以及颅骨照射,并对磁共振成像(MRI)在这种疾病中的价值进行了评论。