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与单克隆丙种球蛋白病相关的肾脏病理表现。

Renal pathologic findings associated with monoclonal gammopathies.

作者信息

Zlotnick A, Rosenmann E

出版信息

Arch Intern Med. 1975 Jan;135(1):40-5.

PMID:803364
Abstract

The myeloma kidney is characterized by casts in the distal and collecting tubules. The glomeruli are hardly affected unless amyloidosis is present. When the glomeruli are involved, the proteinuria is nonselective and, in some cases, the whole paraprotein is excreted in the urine. Nephrocalcinosis may be present and focal myeloma cell infiltration in the interstitium is a characteristic, but inconstant, finding. The nephrotic syndrome is extremely rare; if it exists, amyloidosis should be suspected. In contrast to multiple myeloma, the glomeruli are frequently involved in macroglobulinemia of Waldenstrom. Hyaline intracapillary deposits consisting of pure IgM are a characteristic finding as is infiltration of the kidney with lymphoid cells. No characteristic lesion of the kidney has been described in the heavy-chain diseases. Mixed cryoglobulinemia associated with an IgM paraprotein can produce glomerulonephritis that is due to the deposition in the glomeruli of an immune complex consisting of IgG, IgM, and complement.

摘要

骨髓瘤肾病的特征是远端小管和集合管中有管型。除非存在淀粉样变性,肾小球很少受到影响。当肾小球受累时,蛋白尿是非选择性的,在某些情况下,整个副蛋白会从尿液中排出。可能存在肾钙质沉着症,间质中有局灶性骨髓瘤细胞浸润是其特征性表现,但并不常见。肾病综合征极为罕见;如果存在,应怀疑淀粉样变性。与多发性骨髓瘤不同,华氏巨球蛋白血症时肾小球常受累。由纯IgM组成的透明毛细血管内沉积物是其特征性表现,肾脏有淋巴细胞浸润也是如此。在重链病中尚未描述肾脏的特征性病变。与IgM副蛋白相关的混合性冷球蛋白血症可导致肾小球肾炎,这是由于由IgG、IgM和补体组成的免疫复合物沉积在肾小球所致。

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