原发性多灶性骨淋巴瘤:病例报告和文献综述

IF 0.1 Q4 ONCOLOGY
Christoper A. Alarcon-Ruiz , Dayanne Benites-Gamboa , Ramon Flores-Valdeiglesias , Brady E. Beltran
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引用次数: 0

摘要

原发性骨淋巴瘤(PBL)是一种罕见的起源于髓腔的疾病。病例报告为74岁女性,临床表现为b型症状和双胫骨病理性骨折。核磁共振发现双侧胫骨近端有低信号异质浸润,软组织肿瘤高度摄取,以左腿为主。活检显示弥漫性大b细胞淋巴瘤。患者被诊断为多灶性原发性骨淋巴瘤。据我们所知,这是秘鲁报告的首例病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Linfoma primario óseo multifocal: reporte de caso y revisión de la literatura

Primary bone lymphoma (PBL) is rare disease that originates from the medullary cavity. The case is reported of a 74 year-old woman with a clinical picture characterised by B-symptoms and pathological fracture of both tibias. Nuclear magnetic resonance found a hypointense heterogeneous infiltration in both proximal tibia with high uptake by a soft tissue tumour with predominance in the left leg. The biopsy showed diffuse large B-cell lymphoma. The patient was diagnosed with a multifocal primary bone lymphoma. To our knowledge, it is the first case reported in Peru.

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