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具有不同免疫表型的淋巴结边缘区B细胞淋巴瘤和浆细胞骨髓瘤的共同克隆起源:一例复合淋巴瘤病例报告

A common clonal origin of nodal marginal zone B-cell lymphoma and plasma cell myeloma demonstrating different immunophenotypes: a case report of composite lymphoma.

作者信息

Saito Hajime, Oka Kuniyuki, Nakamura Naoya, Nagayama Reizo, Hakozaki Hando, Mori Naoyoshi

机构信息

Department of Hematology, Mito Saiseikai General Hospital, Mito, Ibaraki, Japan.

出版信息

Diagn Mol Pathol. 2004 Jun;13(2):75-80. doi: 10.1097/00019606-200406000-00003.

Abstract

We demonstrated an 83-year-old male case of composite lymphoma. Before 18 years, he was diagnosed with nodal marginal zone B-cell lymphoma in the cervical lymph node. Peripheral blood showed anemia and IgA (kappa)-type monoclonal gammopathy (IgA; 3,625 mg/dL). Bone marrow aspiration biopsy exhibited plasma cell myeloma, in which atypical plasma cells were positive for cytoplasmic IgA (kappa) and atypical lymphoid cells intermingled were positive for CD20. In contrast, cervical lymph node biopsy revealed nodal marginal zone B-cell lymphoma, in which lymphoma cells were positive for cytoplasmic IgG (lambda). Southern blotting analysis of the IgH gene showed same clonal rearrangement band in both lymph node and bone marrow samples and additional band in the bone marrow. Sequence analyses of the IgH gene showed an identical sequence of CDR3 in both samples. Thus, we demonstrated a common clonal origin of composite lymphoma comprising nodal marginal zone B-cell lymphoma and plasma cell myeloma. Nodal marginal zone B-cell lymphoma recurred in cervical lymph node and involved into the bone marrow, differentiating into plasma cell myeloma in which Ig isotype switched and monoclonal gammopathy developed. Sequence analysis of the IgH gene was a powerful tool for determination of clonal origin.

摘要

我们报告了一例83岁男性复合性淋巴瘤病例。18年前,他被诊断为颈部淋巴结边缘区B细胞淋巴瘤。外周血显示贫血和IgA(κ)型单克隆丙种球蛋白病(IgA;3625mg/dL)。骨髓穿刺活检显示为浆细胞骨髓瘤,其中非典型浆细胞胞质IgA(κ)呈阳性,混杂的非典型淋巴细胞CD20呈阳性。相比之下,颈部淋巴结活检显示为淋巴结边缘区B细胞淋巴瘤,其中淋巴瘤细胞胞质IgG(λ)呈阳性。IgH基因的Southern印迹分析显示,淋巴结和骨髓样本中出现相同的克隆重排条带,骨髓中还有额外条带。IgH基因的序列分析显示,两个样本中CDR3序列相同。因此,我们证实了由淋巴结边缘区B细胞淋巴瘤和浆细胞骨髓瘤组成的复合性淋巴瘤具有共同的克隆起源。淋巴结边缘区B细胞淋巴瘤在颈部淋巴结复发并累及骨髓,分化为Ig同种型转换且出现单克隆丙种球蛋白病的浆细胞骨髓瘤。IgH基因的序列分析是确定克隆起源的有力工具。

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