Doi E, Ozaki F, Yabumoto M, Moriwaki H, Hayashi S, Komai N
No Shinkei Geka. 1983 Jan;11(1):93-8.
Intracerebral schwannoma is very rare, and only nine cases of solitary intracerebral schwannoma have been reported since the first description by Gibson et al, in 1966. This report is the first case of multiple intracerebral schwannomas in Japan. Intracranial extracerebral schwannomas in von Recklinghausen's disease are sometimes encountered, but intracerebral ones have not been discovered. A case of multiple intracerebral schwannomas associated with von Recklinghausen's disease is reported in a 23-year-old male. He had been healthy until January 1979 when he was pointed out an abnormal shadow on chest roentgenogram. Although thoracic tumor revealed schwannoma in histological examination of surgical specimen, it transformed to malignant one during next 15 months. In July 1980, he complained of severe headache, vertigo, nausea and vomiting, and bilateral papilledema was proved. He was admitted to our clinic on August 8, 1980. Two large intracerebellar and four intracerebral tumors were revealed by computed tomography (CT). Angiography demonstrated avascular masses. The cerebellar tumors were totally extirpated on August 12, 1980. Histological diagnosis of the removed tumors approved malignant schwannoma, but their correlation to the chest tumor was unclear. Follow-up CT scans demonstrated that the supratentorial tumors increased in size during about three months. The chest tumor also increases in size. He died on November 12, 1980, but autopsy was not done. Pathogenesis of intracerebral schwannomas in this case is controversial, and we suggest that it is (1) multiple schwannomas in von Recklinghausen's disease with malignant transformation, or (2) metastasis from the chest tumor. But the conclusion remains unclear.
脑内神经鞘瘤非常罕见,自1966年吉布森等人首次描述以来,仅报告了9例孤立性脑内神经鞘瘤。本报告是日本首例多发性脑内神经鞘瘤病例。冯·雷克林豪森病中的颅内脑外神经鞘瘤有时可见,但脑内神经鞘瘤尚未被发现。本文报告了一名23岁男性患有与冯·雷克林豪森病相关的多发性脑内神经鞘瘤。1979年1月胸部X线片发现异常阴影之前他一直健康。虽然手术标本的组织学检查显示胸段肿瘤为神经鞘瘤,但在接下来的15个月内转变为恶性肿瘤。1980年7月,他出现严重头痛、眩晕、恶心和呕吐,并证实有双侧视乳头水肿。1980年8月8日入住我院。计算机断层扫描(CT)显示小脑有两个大肿瘤和四个脑内肿瘤。血管造影显示为无血管肿块。1980年8月12日将小脑肿瘤全部切除。切除肿瘤的组织学诊断为恶性神经鞘瘤,但其与胸段肿瘤的关系尚不清楚。随访CT扫描显示幕上肿瘤在大约三个月内增大。胸段肿瘤也增大。他于1980年11月12日死亡,但未进行尸检。该病例脑内神经鞘瘤的发病机制存在争议,我们认为可能是(1)冯·雷克林豪森病中的多发性神经鞘瘤发生恶性转化,或(2)胸段肿瘤转移。但结论仍不明确。