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伴有高球蛋白血症的蛋白质性淋巴结病。

Proteinaceous lymphadenopathy with hypergammaglobulinemia.

作者信息

Osborne B M, Butler J J, Mackay B

出版信息

Am J Surg Pathol. 1979 Apr;3(2):137-45. doi: 10.1097/00000478-197904000-00004.

DOI:10.1097/00000478-197904000-00004
PMID:532845
Abstract

Three cases of a morphologically distinctive "sclerosis" of lymph nodes are presented. Two patients experienced recurring lymph node enlargement with associated mild malaise over an extended period. The first patient had unilateral axillary lymph node enlargement, but was asymptomatic and died of chronic obstructive pulmonary disease 17 years later with no evidence of lymph node enlargement at autopsy. Each patient had at least transient hypergammaglobulinemia, one with elevated IgM and IgA, one with elevated IgM, and one (from 1958) not further analyzed. Lymph node biopsies revealed extensive deposition of eosinophilic material in all three patients. Identical changes in lymph nodes have been described in chronic diseases. The eosinophilic material may be related to amyloid, but differs from it histochemically and ultrastructurally. The relationship of this lesion to the few cases reported as amyloidosis presenting as lymph node enlargement is discussed. Malignant lymphoma with sclerosis is the most important consideration in the differential diagnosis.

摘要

本文报告了3例形态学上具有独特表现的淋巴结“硬化”病例。2例患者在较长时间内反复出现淋巴结肿大,并伴有轻度不适。首例患者为单侧腋窝淋巴结肿大,但无症状,17年后死于慢性阻塞性肺疾病,尸检时未发现淋巴结肿大迹象。每位患者均至少有过短暂的高球蛋白血症,其中1例IgM和IgA升高,1例IgM升高,另1例(1958年病例)未作进一步分析。3例患者的淋巴结活检均显示有大量嗜酸性物质沉积。慢性疾病中也曾描述过淋巴结的类似改变。这种嗜酸性物质可能与淀粉样蛋白有关,但在组织化学和超微结构上与之不同。本文还讨论了该病变与少数报道为以淋巴结肿大形式出现的淀粉样变性病例之间的关系。鉴别诊断时最重要的考虑因素是伴有硬化的恶性淋巴瘤。

相似文献

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Proteinaceous lymphadenopathy with hypergammaglobulinemia.伴有高球蛋白血症的蛋白质性淋巴结病。
Am J Surg Pathol. 1979 Apr;3(2):137-45. doi: 10.1097/00000478-197904000-00004.
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Immunoblastic lymphadenopathy. A report of two cases.
Arch Pathol Lab Med. 1976 Sep;100(9):465-8.
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Multicentric giant lymph node hyperplasia. A hyperimmune syndrome with a rapidly progressive course.多中心巨大淋巴结增生症。一种病程快速进展的高免疫综合征。
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Angioimmunoblastic lymphadenopathy: a case study.血管免疫母细胞性淋巴结病:病例报告
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Systemic amyloidosis with a mesenteric mass which had the appearance of proteinaceous lymphadenopathy.系统性淀粉样变性伴肠系膜肿块,该肿块表现为蛋白性淋巴结病。
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Lymphadenopathy as a manifestation of amyloidosis: a case series.淋巴结病作为淀粉样变性的一种表现:病例系列
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[Systemic plasmacytosis--syndrome of multiple peculiar skin eruptions, lymphadenopathy and polyclonal hypergammaglobulinemia].[系统性浆细胞增多症——多种特殊皮肤疹、淋巴结病和多克隆高丙种球蛋白血症综合征]
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Ribosome-lamella complex of the lymphocytes in a case of plasmacytic lymphadenopathy with polyclonal hypergammaglobulinemia.一例伴有多克隆高丙种球蛋白血症的浆细胞性淋巴结病中淋巴细胞的核糖体-板层复合体
Ultrastruct Pathol. 1984;6(2-3):161-6. doi: 10.3109/01913128409018570.

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