Saatci I, Baskan O, Haliloglu M, Aydingoz U
Department of Radiology, Hacettepe University Hospital, Ankara, Turkey.
Neuroradiology. 1999 Jun;41(6):443-6. doi: 10.1007/s002340050781.
Langerhans cell histiocytosis (LCH) is a disease of unknown cause characterised by proliferation of histiocytic granulomas in tissues; the primary cerebral manifestation is diabetes insipidus caused by hypothalamic infiltration. We present a patient in whom, except for the absence of high signal on T1 weighting in the posterior pituitary, consistent with central diabetes insipidus, MRI showed no evidence of hypothalamic involvement by histiocytosis, despite the long duration of the disease. However, there was bilateral, symmetrical involvement of the cerebellum and globus pallidus in addition to a calvarial lesion. High signal in the cerebellar white matter on T2-weighted images may represent demyelination, gliosis and cell loss, as previously reported on pathologic examination.
朗格汉斯细胞组织细胞增多症(LCH)是一种病因不明的疾病,其特征是组织中组织细胞肉芽肿增殖;主要的脑部表现是下丘脑浸润导致的尿崩症。我们报告一名患者,除了垂体后叶在T1加权像上无高信号,符合中枢性尿崩症外,尽管病程较长,但MRI未显示组织细胞增多症累及下丘脑的证据。然而,除颅骨病变外,小脑和苍白球出现双侧对称性受累。T2加权像上小脑白质高信号可能代表脱髓鞘、胶质增生和细胞丢失,正如先前病理检查所报道的那样。