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[一例因巨大颅内占位性病变导致颅内高压的多发性骨髓瘤病例]

[A case of multiple myeloma showing intracranial hypertension due to large cranial mass lesions].

作者信息

Sugita K, Kayama T, Ohwada K, Ichinose M, Takasugi R, Ishizaki T

出版信息

No To Shinkei. 1986 Jul;38(7):625-9.

PMID:3756028
Abstract

It is well known that the case of multiple myeloma shows punched-out lesions of the cranium without intracranial hypertension. In this paper a case of multiple myeloma is reported showing intracranial hypertension due to a large tumor that developed in the left parietal bone. There are only 13 case reports about cranial mass lesion of multiple myeloma since 1928. A 52 year-old female was admitted to Iwate Prefectural Isawa Hospital suffering from headache, nausea and vomiting. She had been already diagnosed as multiple myeloma and treated with chemotherapy using Cyclophosphamide, Melphalan and Prednisolone for 2 years. On admission, a large subcutaneous mass was presented on the left parietal region. Craniogram revealed large osteolytic lesion of the left parietal bone and 3 punched-out lesions of the frontal bone. CT scan revealed a large mass lesion in the left epidural space, diploe and subcutaneous space. Angiography showed avascular area. Brain scintigram showed diffuse hot area. Other skeletal bones showed no abnormality. Laboratory examination revealed high concentration of gamma-globulin and high erythrocyte sedimentation rate. Electrophoresis showed high value of immunoglobulin G; immunoglobulin assay was as follows: IgG-6000 mg/dl, IgA-150 mg/dl, IgM-410 mg/dl, IgE-0 mg/dl. Serum electrolytes were within normal limits. Urine didn't include Bence-Jones protein. The patient was diagnosed as multiple myeloma suffering from intracranial hypertension caused by large tumor which developed in the left parietal bone. On the operation, large tumor was existed in the epidural and subcutaneous space invading into the diploe but without infiltration into the dura mater or cerebral cortex.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

众所周知,多发性骨髓瘤病例显示颅骨有筛孔状病变且无颅内高压。本文报告了一例多发性骨髓瘤病例,该病例因左顶骨出现的巨大肿瘤而导致颅内高压。自1928年以来,仅有13例关于多发性骨髓瘤颅骨肿块病变的病例报告。一名52岁女性因头痛、恶心和呕吐入住岩手县磐泽医院。她已被诊断为多发性骨髓瘤,并使用环磷酰胺、美法仑和泼尼松进行了2年的化疗。入院时,左顶区出现一个巨大的皮下肿块。颅骨X线片显示左顶骨有巨大溶骨性病变以及额骨有3个筛孔状病变。CT扫描显示左硬膜外间隙、板障和皮下间隙有一个巨大的肿块病变。血管造影显示无血管区。脑闪烁扫描显示弥漫性热区。其他骨骼未显示异常。实验室检查显示γ球蛋白浓度高和红细胞沉降率高。电泳显示免疫球蛋白G值高;免疫球蛋白检测结果如下:IgG - 6000mg/dl,IgA - 150mg/dl,IgM - 410mg/dl,IgE - 0mg/dl。血清电解质在正常范围内。尿液中未发现本-周蛋白。该患者被诊断为因左顶骨出现的巨大肿瘤导致颅内高压的多发性骨髓瘤。手术时,硬膜外和皮下间隙存在巨大肿瘤,侵入板障,但未浸润至硬脑膜或大脑皮层。(摘要截断于250字)

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