多发性骨髓瘤表现为蝶骨浆细胞瘤:1例报告及文献复习

S. Kadiri
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引用次数: 1

摘要

浆细胞瘤可以表现为单个或多个浆细胞瘤,并可能与多发性骨髓瘤(MM)相关或进展。颅内浆细胞瘤显示多发性骨髓瘤是非常罕见的,只有少数病例在文献报道。我们报告的病例蝶浆细胞瘤显示多发性骨髓瘤在一个56岁的妇女3个月的颞部头痛和复视的历史。磁共振成像(MRI)和计算机断层扫描(CT)显示蝶骨肿块。内镜下蝶窦活检,组织病理学检查显示CD138染色阳性浆细胞瘤。进一步的生物学研究证实了多发性骨髓瘤的诊断,免疫球蛋白(Ig) a的单克隆γ峰。患者开始全身化疗并接受蝶窦减压放疗。患者病情持续缓解8个月后死于肾功能不全。虽然蝶骨浆细胞瘤是一种非常罕见的多发性骨髓瘤的表现,但应考虑有效的患者管理和预后改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiple myeloma revealed by a sphenoid plasmocytoma: case report and literature review
Plasma cell neoplasms can manifest as a solitary or multiple plasmocytomas and may be associated with or progressing to multiple myeloma (MM). Cranial and intracranial plasmocytomas revealing multiple myeloma are very rare and only few cases are reported in the literature. We report the case of a sphenoid plasmocytoma that revealed a multiple myeloma in a 56 year-old woman with 3 months history of temporal headache and diplopia. Magnetic resonance imaging (MRI) and computed tomography (CT) showed a sphenoid mass. An endoscopic sphenoidal biopsy was performed and the histopathological exams showed a plasmocytoma with a positive staining for CD138. Further biological studies confirmed the diagnosis of multiple myeloma with a monoclonal gamma peak of immunoglobulin (Ig) A. The patient started systemic chemotherapy and received decompressive radiation therapy on the sphenoidal sinus. She remained in remission for 8 months and died from renal dysfunction. Although the sphenoid plasmocytoma is a very rare presentation of multiple myeloma it should be considered for effective patient management and prognosis improvement.
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