Udongwo Ndausung, Douedi Steven, Odak Mihir, Alshami Abbas, Patel Swapnil V, Farooq Taliya
Internal Medicine, Jersey Shore University Medical Center, Neptune City, USA.
Pathology, Jersey Shore University Medical Center, Neptune City, USA.
Cureus. 2021 Jul 2;13(7):e16106. doi: 10.7759/cureus.16106. eCollection 2021 Jul.
Multiple myeloma (MM) is a rare plasma cell neoplasm characterized by monoclonal cell infiltration in the bone marrow, which can cause anemia, bone pain, and recurrent infections. Extramedullary myeloma (EM) is a rare clinical presentation with a poor prognosis. It involves the accumulation of clonal plasma cells in soft tissues with a tumor-like appearance, either presenting as a primary (initial) or secondary (relapse) malignancy. We present a case of a 65-year-old male who experienced an abrupt onset of chest pain associated with a localized sternal mass while exercising the day prior to arrival. Chest computed tomography (CT) scan with contrast revealed an expansile lytic lesion around the sternal area. Due to high suspicion for malignancy, a CT-guided core needle biopsy was done, which showed plasma cells with rare Dutcher bodies consistent with MM. Bone marrow smear showed the presence of 70% plasma cells confirming a diagnosis of MM. Early detection of this devastating disease may help improve survival. Therefore, physicians should have a high index of suspicion for MM in older patients with similar clinical presentations.
多发性骨髓瘤(MM)是一种罕见的浆细胞肿瘤,其特征是骨髓中出现单克隆细胞浸润,可导致贫血、骨痛和反复感染。髓外骨髓瘤(EM)是一种罕见的临床表现,预后较差。它表现为克隆性浆细胞在软组织中积聚,呈肿瘤样外观,可表现为原发性(初始)或继发性(复发)恶性肿瘤。我们报告一例65岁男性病例,该患者在入院前一天锻炼时突然出现胸痛,并伴有局部胸骨肿块。胸部增强计算机断层扫描(CT)显示胸骨区域周围有一个膨胀性溶骨性病变。由于高度怀疑为恶性肿瘤,遂进行了CT引导下的粗针活检,结果显示浆细胞伴有罕见的杜氏小体,符合多发性骨髓瘤。骨髓涂片显示70%为浆细胞,确诊为多发性骨髓瘤。早期发现这种毁灭性疾病可能有助于提高生存率。因此,医生对具有类似临床表现的老年患者应高度怀疑多发性骨髓瘤。