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Unusual presentation of more common disease/injury: Ophthalmic manifestations of atypical IgD multiple myeloma

机译:不常见的疾病/伤害表现:非典型IgD多发性骨髓瘤的眼科表现

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摘要

A previously healthy 32-year-old Caucasian female presented with sudden-onset horizontal diplopia following a paroxysm of coughing. She had recently sustained a pubic ramus fracture during an innocuous fall and had also noted a firm lump developing at the right side of her forehead. On examination, she had a right fronto-temporal mass. Visual acuities were 6/6 bilaterally. There was reduced abduction of the right eye, bilateral white, granular corneal opacities and evidence of bilateral optic disc swelling. Haematological investigations revealed normocytic anaemia, hypercalcaemia and raised erythrocyte sedimentation rate (ESR). CT showed lytic foci throughout the skull, ribs, scapulae, spine, pelvis and upper femora. Serum protein electrophoresis revealed immunoglobulin D (IgD)-kappa paraproteinaemia; urine electrophoresis showed free light chain kappa and bone marrow biopsy demonstrated 87% plasma cells. A diagnosis of IgD multiple myeloma was made, with subsequent chemotherapeutic treatment and eventual autologous stem cell transplant resulting in resolution of neuro-ophthalmic manifestations and prolonged disease remission.
机译:一名先前健康的32岁白人女性在咳嗽发作后出现突然发作的水平复视。最近,她在无痛的跌倒时发生了耻骨下支骨折,并且还注意到额头右侧出现坚硬的肿块。经检查,她的额颞部肿块正确。双侧视力为6/6。右眼外展减少,双侧白色,角膜颗粒状混浊,双侧视盘红肿的证据。血液学调查显示正常血性贫血,高钙血症和红细胞沉降率(ESR)升高。 CT显示在整个颅骨,肋骨,肩骨,脊柱,骨盆和股骨上段有溶解灶。血清蛋白电泳显示免疫球蛋白D(IgD)-κ副蛋白血症;尿电泳显示游离轻链κ,骨髓活检显示87%的浆细胞。诊断为IgD多发性骨髓瘤,随后进行化学疗法治疗并最终进行自体干细胞移植,从而导致神经眼病症状消退并延长了疾病的缓解期。

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