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Plasmacytoma of the Clivus Presenting as Bilateral Sixth Nerve Palsy

机译:表现为双侧第六神经麻痹的Cl肌浆细胞瘤

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>Background and Importance Plasmacytomas are monoclonal proliferations of plasma cells that may arise within soft tissue or bone. The skull base is a rare site for plasmacytomas to occur, and few cases have been reported in the literature. When present in the skull base, plasmacytomas may result in cranial neuropathies and often progress to multiple myeloma more rapidly than other intracranial or skeletal plasmacytomas. >Clinical Presentation A 69-year-old man presented with a primary complaint of diplopia and an examination consistent with bilateral abducens nerve palsy. No other deficits were noted. Magnetic resonance imaging of the skull base demonstrated a large T1 isointense moderately enhancing lesion centered within the clivus. Endoscopic biopsy of the mass revealed sheets and aggregates of mature monoclonal plasma cells. The patient's initial systemic work-up revealed that this was a solitary lesion, and he was treated with radiation therapy to the skull base with a durable local effect at 18-month follow-up. Unfortunately he progressed to multiple myeloma with peripheral osteolytic lesions but has been stabilized on chemotherapeutics. >Conclusion The clivus is an unusual site for intracranial plasmacytomas, and enhancing lesions must be differentiated from chordoma. Characteristic findings on histopathology include an immunoglobulin light-chain restricted clonal proliferation of plasma cells. Treatment is most commonly radiotherapy with surgery reserved for biopsy and palliation. Clinicians should be aware of the increased risk of progression to multiple myeloma in skull base plasmacytomas.
机译:>背景和重要性浆细胞瘤是浆细胞的单克隆增殖,可能在软组织或骨骼内产生。颅底是浆细胞瘤发生的罕见部位,文献报道的病例很少。当存在于颅底时,浆细胞瘤可导致颅神经病,并且通常比其他颅内或骨骼浆细胞瘤更快地发展为多发性骨髓瘤。 >临床表现一名69岁的男性患者,其主要表现为复视并接受了与双侧外展神经麻痹相符的检查。没有发现其他缺陷。颅底的磁共振成像显示,大的T1等强度适度增强了以锁骨为中心的病变。肿块的内窥镜活检显示出成熟的单克隆浆细胞的薄片和聚集体。患者最初的全身检查表明这是一个孤立的病灶,在18个月的随访中对他的颅底进行了放射治疗,并产生了持久的局部作用。不幸的是,他发展为多发性骨髓瘤并伴有周围溶骨性病变,但已在化疗药物上稳定下来。 >结论 cl骨是颅内浆细胞瘤的异常部位,必须将增强病变与脊索瘤区分开。组织病理学的特征发现包括浆细胞的免疫球蛋白轻链限制的克隆增殖。最常见的治疗方法是放疗,保留活检和姑息术。临床医生应意识到颅底浆细胞瘤进展为多发性骨髓瘤的风险增加。

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