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多发性骨髓瘤的一种不寻常表现:一名71岁女性,其四肢骨骼有单个溶骨性病变。

An Unusual Presentation of Multiple Myeloma: A 71-Year-Old Female With a Single Lytic Lesion of Her Appendicular Skeleton.

作者信息

Khalyfa Ahamed, Carrillo Alessandra C, Chavis Yhana

机构信息

Internal Medicine, Franciscan Health, Olympia Fields, USA.

出版信息

Cureus. 2022 May 4;14(5):e24725. doi: 10.7759/cureus.24725. eCollection 2022 May.

Abstract

Multiple myeloma is a devastating illness with a hallmark of end-organ damage. The clinical presentation of multiple myeloma often includes the involvement of CRAB (hypercalcemia, renal failure, anemia, bone lesions) symptoms. We present a case of a patient who did not exhibit the typical presentation of multiple myeloma making her case unique and her diagnosis more difficult. In addition to the CRAB criteria, typical symptomatology includes constipation, pain, fatigue, and peripheral sensory issues. The purpose of this case report is to bring awareness to both multiple myeloma and this particular presentation. The patient is a 71-year-old female with a past medical history of hypertension, hypothyroidism, and rheumatoid arthritis who presented with a chief complaint of right shoulder pain. The patient's initial labs were significant for a total protein of 9.3, albumin of 3.4, corrected calcium of 9.3, hemoglobin 10.6 (with baseline near 11-12), and creatinine of 1.0 (baseline of 1.0). The patient's right upper extremity X-rays were significant for a right humeral fracture. The patient had a serum kappa/lambda ratio of 15.94. Bone marrow biopsy revealed 50% kappa-restricted cells, consistent with a diagnosis of multiple myeloma. The patient's subsequent bone survey and CT scan were negative for any additional lesions. The patient had subsequent radiation therapy followed by maintenance therapy with bortezomib, lenalidomide, and dexamethasone with improvement in her symptoms. MM is a complex pathophysiological disease and equally as complex in diagnosis as the presentation is varied and sometimes obscure as noted in the case presented here. Although bone lytic lesions are part of the CRAB criteria, it is rare for them to present in patients with MM in an isolated manner with no corresponding lab abnormalities. With this case, we aim to shed light upon an atypical presentation of MM, notably one that solely involves a pathological fracture in a non-axial distribution.

摘要

多发性骨髓瘤是一种具有终末器官损害特征的毁灭性疾病。多发性骨髓瘤的临床表现通常包括CRAB(高钙血症、肾衰竭、贫血、骨病变)症状。我们报告一例未表现出多发性骨髓瘤典型症状的患者,这使得她的病例较为独特且诊断更加困难。除了CRAB标准外,典型症状还包括便秘、疼痛、疲劳和周围感觉问题。本病例报告的目的是提高对多发性骨髓瘤及其这种特殊表现的认识。该患者为71岁女性,既往有高血压、甲状腺功能减退和类风湿关节炎病史,主要主诉为右肩疼痛。患者最初的实验室检查结果显示总蛋白为9.3,白蛋白为3.4,校正钙为9.3,血红蛋白10.6(基线接近11 - 12),肌酐为1.0(基线为1.0)。患者右上肢X线检查显示右肱骨骨折。患者血清κ/λ比值为15.94。骨髓活检显示50%的κ限制性细胞,符合多发性骨髓瘤的诊断。患者随后的骨扫描和CT扫描未发现其他病变。患者随后接受了放射治疗,之后接受硼替佐米、来那度胺和地塞米松维持治疗,症状有所改善。多发性骨髓瘤是一种复杂的病理生理疾病,其诊断同样复杂,因为临床表现多样,有时如本病例所示较为隐匿。虽然溶骨性病变是CRAB标准的一部分,但在多发性骨髓瘤患者中单独出现且无相应实验室异常的情况很少见。通过这个病例,我们旨在揭示多发性骨髓瘤的一种非典型表现,特别是仅涉及非轴向分布的病理性骨折的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/850a/9165616/afa6dda4f762/cureus-0014-00000024725-i01.jpg

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