Persistent Abdominal Pain with an Uncommon Presentation of Multiple Myeloma: A Case Study

Bounouar Ibtissam, Boumaazi Hiba, ElManjra Chama, Nacir Oussama, Lairani Fatima Ezzahra, AitErrami Adil, Sayagh Sanae, Oubaha Sophia, Samlani Zouhour, Krati Khadija
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Abstract

Multiple myeloma (MM) is a widespread malignant condition characterized by the proliferation of transformed plasma cells in the bone marrow, disrupting its normal functions and infiltrating adjacent bone tissues. While typically confined to the bone marrow, in rare instances, patients may develop extramedullary disease. In these uncommon scenarios, the involvement of lymph nodes poses a diagnostic challenge for practitioners in their daily routines. This report details the case of a 49-year-old male experiencing chronic abdominal pain. A computed tomography (CT) scan revealed enlargement of retroperitoneal and mesenteric lymph nodes. Biopsies confirmed a plasma cell infiltrate positive for CD138 and kappa light chain, leading to the diagnosis of multiple myeloma with extramedullary localization in lymph nodes. Our case underscores the rare presentation of extramedullary involvement in multiple myeloma, characterized by an atypical clinical manifestation.
多发性骨髓瘤罕见表现的持续性腹痛:病例研究
多发性骨髓瘤(MM)是一种广泛存在的恶性疾病,其特点是转化的浆细胞在骨髓中增殖,破坏骨髓的正常功能并浸润邻近的骨组织。虽然骨髓瘤通常局限于骨髓,但在极少数情况下,患者可能会出现髓外疾病。在这些不常见的情况下,淋巴结受累会给医生的日常诊断带来挑战。本报告详述了一名 49 岁男性的慢性腹痛病例。计算机断层扫描(CT)显示腹膜后和肠系膜淋巴结肿大。活检证实浆细胞浸润,CD138 和 kappa 轻链阳性,诊断为淋巴结髓外定位的多发性骨髓瘤。我们的病例强调了多发性骨髓瘤髓外受累的罕见表现,其特点是临床表现不典型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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