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成人范科尼综合征与多发性骨髓瘤

Adult Fanconi syndrome and multiple myelomatosis.

作者信息

Horn M E, Knapp M S, Page F T, Walker W H

出版信息

J Clin Pathol. 1969 Jul;22(4):414-6. doi: 10.1136/jcp.22.4.414.

Abstract

A case is described of a 59-year-old woman presenting with multiple renal tubular defects. The aminoaciduria was of a generalized type. When investigated initially the only feature of myelomatosis was urinary Bence-Jones protein. Two years later radiologically classical multiple myelomatosis developed and rapidly progressed to the patient's death nine months later.

摘要

本文描述了一例59岁女性,其表现为多种肾小管缺陷。氨基酸尿为全身性类型。最初检查时,骨髓瘤病的唯一特征是尿本-周蛋白。两年后,影像学显示典型的多发性骨髓瘤病,九个月后病情迅速进展导致患者死亡。

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Adult Fanconi syndrome and multiple myelomatosis.成人范科尼综合征与多发性骨髓瘤
J Clin Pathol. 1969 Jul;22(4):414-6. doi: 10.1136/jcp.22.4.414.

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