Jaeger P, Bonafe A, Fraysse B, Manelfe C
Service de Neuroradiologie, Hôpital Purpan, Toulouse.
J Radiol. 1993 May;74(5):283-90.
Two cases are reported of histiocytosis X in young adults, both confined to the petrous bone. In one case the clinical signs were those of a progressive facial palsy, developing over 3 years; the other case had pulsatile tinnitus with clear otorrhoea and symptoms of vestibular deficiency. Computed tomography showed extensive bone destruction by a soft-tissue density process which enhanced strongly after iodinated contrast injection. Magnetic resonance imaging (T1 weighted sequences before and after intravenous gadolinium injection) confirmed the presence of a mass lesion in the petrous bone with contrast medium uptake which showed cystic areas within it: it also showed the absence of extension through the dura mater by the intracranial component which remained extradural. It confirmed the patency of arteries and veins, so enabling a differentiation to be made between histiocytosis X and advanced glomus tumours.
报告了两例发生在青年成人中的组织细胞增多症X,病变均局限于岩骨。一例临床症状为进行性面神经麻痹,病程3年;另一例有搏动性耳鸣、清亮耳漏及前庭功能减退症状。计算机断层扫描显示软组织密度影广泛破坏骨质,注射碘化造影剂后强化明显。磁共振成像(静脉注射钆前后的T1加权序列)证实岩骨有一肿块性病变,摄取造影剂,内部可见囊性区域;还显示颅内部分未穿过硬脑膜,仍位于硬膜外。它证实了动静脉通畅,从而能够区分组织细胞增多症X和晚期颈静脉球瘤。