IgG-k/IgG-λ副骨浆细胞瘤复发为具有 IgA-k 免疫表型的软组织浆细胞瘤:病例报告及相关生化方面的文献综述。

IF 1.1 Q4 HEMATOLOGY
Manlio Fazio, Chiara Maria Catena Sorbello, Vittorio Del Fabro, Alessandra Romano, Maria Teresa Cannizzaro, Nunziatina Laura Parrinello, Benedetta Esposito, Sara Frazzetto, Federica Elia, Francesco Di Raimondo, Concetta Conticello
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引用次数: 0

摘要

髓外多发性骨髓瘤(EMD)是指肿瘤性浆细胞(PCs)在骨髓(BM)脱位的解剖部位增殖,或从破坏骨皮质的骨质病变处毗连生长。从治疗和生物学角度来看,髓外多发性骨髓瘤仍具有挑战性。其发病机制尚未完全明确,通常与高危细胞遗传学(HRCA)有关。为了强调这种疾病在临床和生化方面的复杂性,我们决定描述一例复发-难治性(RR)EMD 患者的病例,该患者表现为具有双表型免疫球蛋白(Ig)成分的骨旁浆细胞瘤,最近复发为具有完全免疫表型转换的软组织浆细胞瘤。我们还假设了 Ig 模式与预后之间的相关性,并建议将这些生化特征纳入一般风险评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
IgG-k/IgG-λ Para-Osseous Plasmacytoma Relapsed as Soft-Tissue Plasmacytoma with IgA-k Immunophenotype: A Case Report and Review of the Literature on Related Biochemical Aspects.

Neoplastic plasma cells (PCs) proliferation at anatomic sites dislocated from the bone marrow (BM) or their contiguous growth from osseous lesions that disrupt the cortical bone is termed extramedullary multiple myeloma (EMD). EMD still remains challenging from a therapeutic and biological perspective. Pathogenesis has not been completely clarified, and it is generally associated with high-risk cytogenetics (HRCAs). In order to emphasize the clinical and biochemical complexity of this disease, we have decided to describe the case of a patient affected by relapsed-refractory (RR) EMD, which presented as para-osseous plasmacytoma with a bi-phenotypical immunoglobulin (Ig) component and lately relapsed as soft-tissue plasmacytoma with a total immunophenotype switch. We have also hypothesized a correlation between Ig patterns and prognosis and suggested the possible inclusion of these biochemical features in the general risk assessment.

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来源期刊
Hematology Reports
Hematology Reports HEMATOLOGY-
CiteScore
0.90
自引率
0.00%
发文量
47
审稿时长
10 weeks
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