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Multiple Myeloma Presenting as Bilateral Posterior Optic Neuropathy

机译:多发性骨髓瘤表现为双侧后视神经病变

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We report a case of bilateral posterior optic neuropathy as the presenting sign of multiple myeloma. A 72-year-old woman experienced bilateral progressive visual loss leading to blindness in 1 week without optic disc swelling. Brain and orbit magnetic resonance imaging revealed thickening of both intracranial optic nerves with abnormal sheath enhancement in post-contrast sequences. Systemic work-up detected a monoclonal band in blood and urine, and skeletal survey showed lytic lesions in the skull bones and multiple collapsed vertebrae. Bone marrow biopsy revealed atypical plasma cells. On the basis of these findings the diagnosis of multiple myeloma was made even though there was neither hypercalcemia nor renal failure. The mechanism of visual loss is a presumed infiltration of the intracranial optic nerves and the adjacent meningeal coverings.
机译:我们报告一例双侧后视神经病变为多发性骨髓瘤的表现体征。一名72岁的妇女经历了双侧进行性视力丧失,导致1周内失明,无视盘肿胀。脑部和眶部磁共振成像显示,在对比后序列中,颅内视神经均增厚,鞘层异常增强。全身检查发现血液和尿液中有一条单克隆谱带,骨骼检查显示颅骨内有溶解性病变,多处椎骨塌陷。骨髓活检显示非典型浆细胞。基于这些发现,即使既没有高钙血症也没有肾衰竭,但仍诊断出多发性骨髓瘤。视力丧失的机制是推测的颅内视神经和邻近的脑膜覆盖物浸润。

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