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A case report of POEMS syndrome with renal involvement as immunotactoid glomerulopathy

机译:肾脏受累为免疫性类脂性肾小球病的POEMS综合征一例报告

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Rationale: POEMS syndrome is a rare multi-system disorder, which sometimes involves the kidney. Immunotactoid glomerulopathy (ITG) is an uncommon glomerular disease resulted from deposits of immunoglobulins and its derivatives. ITG caused by POEMS syndrome is rarely reported. Patient concerns: A 63-year-old man was presented with acute kidney injury. In addition, it's found that he had abnormal serum free κ /λ ratio, polyneuropathy, Castleman's disease, organomegaly, endocrinopathy and skin changes. Diagnoses: POEMS syndrome was diagnosed, Renal biopsy revealed an ITG. Interventions: Dexamethasone and thalidomide were given, as well as hemodialysis and other supportive treatments. Outcomes: The patient's extrarenal manifestations improved gradually and his renal function also showed slight improvement. Lessons: ITG caused by POEMS syndrome is rare, however, it makes sense that the monoclonal proteins produced by the plasma cells could cause ITG. Chemotherapy similar to that employed in multiple myeloma may be beneficial for these patients.
机译:理由:POEMS综合征是一种罕见的多系统疾病,有时涉及肾脏。免疫非球体性肾小球疾病(ITG)是由免疫球蛋白及其衍生物沉积导致的罕见肾小球疾病。由POEMS综合征引起的ITG报道很少。病人担忧:一名63岁的男子患有急性肾损伤。另外,发现他的血清游离κ/λ比,多发性神经病,Castleman病,器质性肿大,内分泌病和皮肤变化异常。诊断:诊断为POEMS综合征,肾活检显示为ITG。干预措施:给予地塞米松和沙利度胺,以及血液透析和其他支持治疗。结果:患者的肾外表现逐渐改善,肾脏功能也略有改善。经验教训:由POEMS综合征引起的ITG很少,但是,浆细胞产生的单克隆蛋白可能引起ITG是有道理的。与多发性骨髓瘤相似的化学疗法可能对这些患者有益。

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