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导致低钾性肾病和致命性肠穿孔的α链病。

alpha-Chain disease causing kaliopenic nephropathy and fatal intestinal perforations.

作者信息

Economidou J C, Manousos O N, Katsaros D

出版信息

Am J Dig Dis. 1976 Jul;21(7):577-85. doi: 10.1007/BF01464766.

Abstract

A case of alpha-chain disease (alpha-CD) is described presenting as a malabsorption syndrome complicated by severe kalipenic nephropathy. Antibiotics and cyclophosphamide were effective in controlling the malabsorption and thr renal dysfunction but did not affect the basic pathological lesion. Eventually the disease became generalized, affected lymph nodes, liver and bone marrow and caused multiple intestinal perforations. Detailed histological studies failed to demonstrate the development of reticulum-cell sarcoma as a terminal complication of the disease and are suggestive of a single malignant plasmacytic cell process.

摘要

本文描述了一例α链病(α-CD),其表现为吸收不良综合征并伴有严重低钾性肾病。抗生素和环磷酰胺可有效控制吸收不良和肾功能不全,但未影响基本病理病变。最终,疾病全身播散,累及淋巴结、肝脏和骨髓,并导致多处肠穿孔。详细的组织学研究未能证实网状细胞肉瘤作为该疾病的终末期并发症的发生,提示这是一个单一的恶性浆细胞过程。

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