Zaidi Saba, Sattar Sidra, Asumal Khealani Bhojo
Department of Neurology, The Aga Khan University Hospital, Karachi.
Department of Community Health Sciences, Ziauddin University Hospital, Karachi.
J Coll Physicians Surg Pak. 2017 Oct;27(10):651-653.
POEMS (acronym for polyneuropathy, organomegaly, endocrinopathy, M protein myeloma and skin changes), is a rare disease which occurs in the setting of plasma cell dyscrasias. We describe a case of an adult lady who presented with gradual onset weakness of all four limbs and multisystem involvement characterized by pedal edema, ascites, hyperpigmentation and hypogonadism. Nerve conduction study showed severe sensorimotor polyneuropathy. Serum immunofixation showed lambda light chain restricted monoclonal gammopathy. Bone marrow biopsy consistent with plasma cell dyscrasia. Hormonal assay showed decreased FSH, LH and estradiol levels which led us to diagnosis of hypogonadotrophic hypogonadism. The patient responded well to combination therapy of thalidomide, melphalan and dexamethasone. Eight months after the therapy, she noted decreased paresthesias and increased strength. She had reduced edema and ascites.
POEMS综合征(多神经病、器官肿大、内分泌病、M蛋白血症和皮肤改变的首字母缩写)是一种发生于浆细胞发育异常情况下的罕见疾病。我们报告一例成年女性病例,该患者表现为四肢逐渐出现无力以及多系统受累,特征为足部水肿、腹水、色素沉着和性腺功能减退。神经传导检查显示严重的感觉运动性多神经病。血清免疫固定电泳显示λ轻链限制性单克隆丙种球蛋白病。骨髓活检结果符合浆细胞发育异常。激素检测显示促卵泡生成素、促黄体生成素和雌二醇水平降低,这使我们诊断为低促性腺激素性性腺功能减退。该患者对沙利度胺、美法仑和地塞米松联合治疗反应良好。治疗八个月后,她感觉感觉异常减轻,力量增强。水肿和腹水也有所减轻。