Limaiem Faten, Gharbi Mohamed Amine, Bouzidi Ramzi
University of Tunis El Manar, Faculty of Medicine of Tunis, Tunisia; Pathology Department, Hospital Mongi Slim, La Marsa, Tunisia.
University of Tunis El Manar, Faculty of Medicine of Tunis, Tunisia; Department of Orthopedic Surgery, Hospital Mongi Slim, La Marsa, Tunisia.
Int J Surg Case Rep. 2025 Aug 16;135:111829. doi: 10.1016/j.ijscr.2025.111829.
Extramedullary multiple myeloma is a rare condition, occurring in 7 % to 18 % of cases, where malignant plasma cells spread beyond the bone marrow to various organs and soft tissues. This report presents a case of secondary extramedullary multiple myeloma with an unusual soft tissue mass, highlighting diagnostic challenges, management considerations, and the importance of early detection.
A 78-year-old woman with a history of multiple myeloma and AL amyloidosis presented with a rapidly enlarging, non-tender gluteal mass over the past two months. Physical examination disclosed a firm, non-tender mass palpable in the left buttock, measuring approximately 23 cm. Imaging revealed osteolytic lesions in the left hip and a large mass invading surrounding tissues. A surgical biopsy was performed. Histological examination revealed a highly cellular malignant proliferation composed of atypical plasma cells arranged in sheets, surrounded by a thick fibrous capsule. Immunohistochemistry showed strong CD138 positivity, confirming the diagnosis of extramedullary plasmacytoma. The patient was scheduled for adjuvant radiotherapy but passed away due to severe pneumonia shortly after the first session of treatment.
The case underscores the diagnostic challenges and importance of a comprehensive evaluation in extramedullary multiple myeloma. Early detection and appropriate management are crucial for optimal patient care.
This case highlights the significance of recognizing and managing extramedullary multiple myeloma, particularly in patients with uncommon soft tissue presentations. Comprehensive evaluation and timely intervention are essential for enhancing patient outcomes in such cases.
髓外多发性骨髓瘤是一种罕见疾病,发生率为7%至18%,恶性浆细胞扩散至骨髓以外的各种器官和软组织。本报告介绍了一例继发性髓外多发性骨髓瘤病例,该病例伴有不寻常的软组织肿块,强调了诊断挑战、管理考量以及早期检测的重要性。
一名78岁女性,有多发性骨髓瘤和AL淀粉样变性病史,在过去两个月中出现一个迅速增大、无压痛的臀部肿块。体格检查发现左侧臀部可触及一个质地坚硬、无压痛的肿块,大小约为23厘米。影像学检查显示左髋部有溶骨性病变,以及一个侵犯周围组织的大肿块。进行了手术活检。组织学检查显示高度细胞性的恶性增殖,由成片排列的非典型浆细胞组成,周围有一层厚厚的纤维包膜。免疫组织化学显示CD138强阳性,确诊为髓外浆细胞瘤。患者原定接受辅助放疗,但在第一次治疗后不久因严重肺炎去世。
该病例强调了髓外多发性骨髓瘤诊断的挑战以及全面评估的重要性。早期检测和适当管理对于优化患者护理至关重要。
本病例突出了认识和管理髓外多发性骨髓瘤的重要性,特别是在具有不常见软组织表现的患者中。全面评估和及时干预对于改善此类病例的患者预后至关重要。