Mindermann Thomas
Neurosurgery, Klinik Im Park, Seestrasse 220, 8027 Zurich, Switzerland.
Surg Neurol Int. 2016 Dec 20;7:106. doi: 10.4103/2152-7806.196238. eCollection 2016.
There are only few reports on distant metastases of cranial meningiomas WHO I. In one-third of the cases, distant metastases seem to be clinically silent. This is the first case of distant metastases which may have manifested with a paraneoplastic syndrome.
A 52-year-old white male patient was diagnosed with distant metastases to the bones and liver 11 and 12 years following craniotomy and removal of a tentorial meningioma WHO I. At that time, the patient had developed paresthesia, unsteady gait, and a slight cognitive impairment, which in retrospect had no other explanation than that of a paraneoplastic syndrome. Eighteen years following craniotomy, a small intracranial tumor rest is under control following two single session radiosurgery treatments. At present, the patient has a multitude of bone and liver metastases, which seem to cause his paraneoplastic symptoms.
Screening for malignancies in patients with paraneoplastic symptoms and a history of cranial meningioma should include screening for distant metastases from the meningioma.
关于世界卫生组织I级颅脑膜瘤远处转移的报道较少。在三分之一的病例中,远处转移在临床上似乎没有症状。这是首例可能表现为副肿瘤综合征的远处转移病例。
一名52岁的白人男性患者在开颅切除世界卫生组织I级小脑幕脑膜瘤11年和12年后被诊断出骨骼和肝脏远处转移。当时,患者出现感觉异常、步态不稳和轻度认知障碍,回顾起来,除了副肿瘤综合征外没有其他解释。开颅术后18年,经过两次单次放射外科治疗,颅内残留的小肿瘤得到控制。目前,患者有多处骨骼和肝脏转移,似乎导致了他的副肿瘤症状。
对于有副肿瘤症状且有颅脑膜瘤病史的患者,恶性肿瘤筛查应包括对脑膜瘤远处转移的筛查。