[遗传性球形红细胞增多症合并本-周蛋白型多发性骨髓瘤：一例报告] - Suppr | 超能文献

[Hereditary spherocytosis associated with Bence Jones type multiple myeloma: a case report].

作者信息

Hattori Y, Harada K

出版信息

Rinsho Ketsueki. 1988 Feb;29(2):254-7.

Abstract

摘要

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[Hereditary spherocytosis associated with Bence Jones type multiple myeloma: a case report].[遗传性球形红细胞增多症合并本-周蛋白型多发性骨髓瘤：一例报告]

Rinsho Ketsueki. 1988 Feb;29(2):254-7.

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[Clinical importance of paraprotein of the type kappa and lambda in Bence-Jones myeloma].[κ型和λ型副蛋白在本斯-琼斯骨髓瘤中的临床重要性]

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[Primary amyloidosis and thrombophlebitis as complications of Bence-Jones plasmacytoma (lambda type)].[原发性淀粉样变性和血栓性静脉炎作为本斯-琼斯浆细胞瘤（λ型）的并发症]

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Polymeric (presumed tetrameric) lambda Bence Jones proteinemia without proteinuria in a patient with multiple myeloma.一名多发性骨髓瘤患者出现聚合性（推测为四聚体）λ本-周蛋白血症但无蛋白尿。

Am J Clin Pathol. 1984 Nov;82(5):627-9.

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Challenges of Managing Multiple Myeloma Patients with Sickle Cell Disease: A Case Report and Review of Literature.多发性骨髓瘤伴镰状细胞病患者的管理挑战：病例报告及文献复习。

Am J Case Rep. 2021 Dec 29;22:e933470. doi: 10.12659/AJCR.933470.