Aikawa S, Morimoto K, Kumagai T, Saitoh T, Tsuboi I, Sawada U, Horie T
First Department of Internal Medicine, Nihon University School of Medicine.
Rinsho Ketsueki. 1998 Jul;39(7):506-11.
A 30-year-old man who had been given a diagnosis of IgG-kappa multiple myeloma by another hospital and treated with melphalan, prednisone, and cyclophosphamide 6 months earlier, was admitted to our hospitaly in July 1994 because of progressively impaired hearing in both ears, vertigo, and worsening fatigue. Peripheral blood examination showed a white blood cell count 25,000/microliter, with 77.5% atypical plasma cells. Examination at the time of hospitalization also revealed retinal hemorrhages and serum hyperviscosity. The diagnosis was plasma cell leukemia with hyperviscosity syndrome. Subsequent treatment consisted of vincristine, doxorubicine, and prednisone and repeated plasmapheresis. This resulted in a partial response and a reduction of serum viscosity but no reversal of hearing loss. One month after admission, left sixth cranial nerve plasy was demonstrated. Cranial computed tomography studies disclosed a tumoral mass in the sphenoid sinus. The patient received local radiotherapy and intensive chemotherapy, but exhibited no notable alleviation of his cranial nerve palsy. He died of septicemia and progressive disease in August 1994. This case was rare in that it involved plasma cell leukemia and bilateral neurosensory hearing loss associated with serum hyperviscosity and sixth cranial nerve plasy due to plasmacytoma within the sphenoid sinus.
一名30岁男性,6个月前被另一家医院诊断为IgG-κ型多发性骨髓瘤,并接受了美法仑、泼尼松和环磷酰胺治疗。1994年7月因双耳听力逐渐受损、眩晕和疲劳加重入住我院。外周血检查显示白细胞计数为25,000/微升,非典型浆细胞占77.5%。住院时检查还发现视网膜出血和血清高粘滞度。诊断为浆细胞白血病伴高粘滞综合征。随后的治疗包括长春新碱、阿霉素和泼尼松,并反复进行血浆置换。这导致了部分缓解和血清粘度降低,但听力损失没有逆转。入院1个月后,发现左侧第六颅神经麻痹。头颅计算机断层扫描研究显示蝶窦有肿瘤肿块。患者接受了局部放疗和强化化疗,但颅神经麻痹没有明显缓解。他于1994年8月死于败血症和疾病进展。该病例罕见之处在于它涉及浆细胞白血病以及与血清高粘滞度相关的双侧神经性听力损失,还有蝶窦内浆细胞瘤导致的第六颅神经麻痹。