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[以鞍旁综合征和颅神经麻痹为表现的多发性骨髓瘤]

[Multiple myeloma presenting as parasellar syndrome and cranial nerve palsies].

作者信息

Kanoh T, Okuda T, Hayashi M, Yumoto Y

机构信息

Department of Internal Medicine, Kyoto University, Japan.

出版信息

Rinsho Ketsueki. 1996 Mar;37(3):260-4.

PMID:8727353
Abstract

Cranial and intracranial locations have been rarely reported in multiple myeloma. Their occurrence as a harbinger of multiple myeloma seems to have a particular significance. In this report, we discuss a case of multiple myeloma presenting as parasellar syndrome and cranial nerve palsies. A 75-year-old woman was admitted to the hospital in June, 1994, with a 3-month history of headache and a 3-week history of diplopia and photophobia. Physical examination revealed right third, fourth and sixth cranial nerve palsies. MRI scan demonstrated a homogeneous, voluminous mass, isointense in T1-weighted images with the cerebral parenchyma and hyperintense in T2-weighted images, occupying the sphenoid sinus and extending within the sella turcica and right cavernous sinus. Lying above the mass and apparently separated from it by a thin rim of hypointensity was a normal pituitary gland. X rays revealed destructive changes of the sella turcica. A minimal disturbance of endocrine function together with a radiologically abnormal pituitary fossa indicated that the primary lesion might lie outside the pituitary fossa. A diagnosis of IgG-kappa type multiple myeloma was made by pertinent laboratory studies. She received local radiation to the intracranial mass (50 Gy) and conventional chemotherapy. Sixteen months after the therapy she is in good health.

摘要

多发性骨髓瘤累及颅骨及颅内的情况鲜有报道。其作为多发性骨髓瘤的先兆出现似乎具有特殊意义。在本报告中,我们讨论一例以鞍旁综合征及颅神经麻痹为表现的多发性骨髓瘤病例。一名75岁女性于1994年6月入院,有3个月头痛病史及3周复视和畏光病史。体格检查发现右侧动眼神经、滑车神经及展神经麻痹。MRI扫描显示一均匀、巨大肿块,在T1加权像上与脑实质等信号,在T2加权像上呈高信号,占据蝶窦并延伸至蝶鞍及右侧海绵窦内。肿块上方有一正常垂体,二者之间可见一薄层低信号影将其分隔。X线显示蝶鞍骨质破坏。内分泌功能轻度紊乱及放射学上垂体窝异常提示原发病变可能位于垂体窝外。通过相关实验室检查确诊为IgG-κ型多发性骨髓瘤。她接受了颅内肿块局部放疗(50 Gy)及常规化疗。治疗16个月后,她身体健康。

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