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一名因卵巢癌接受卡铂治疗的女性发生硬皮病伴血栓性微血管病导致的肾衰竭。

Renal failure due to scleroderma with thrombotic microangiopathy developing in a woman treated with carboplatin for ovarian cancer.

作者信息

Karim M, Vaux E, Davies D R, Mason P D

机构信息

Oxford Kidney Unit, Churchill Hospital, UK.

出版信息

Clin Nephrol. 2002 Nov;58(5):384-8. doi: 10.5414/cnp58384.

Abstract

Acute renal failure in association with microangiopathic hemolytic anemia and the pathological finding of thrombotic microangiopathy may occur in a number of conditions including hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, and systemic sclerosis. Distinguishing between these conditions on clinical grounds may be difficult, and further investigations, including serological tests, are normally helpful. We present a patient who was treated with 5 doses of monthly carboplatin chemotherapy for stage IIb ovarian carcinoma and who subsequently developed acute renal failure and microangiopathic hemolysis together with some cutaneous features of systemic sclerosis. Initial serological tests, including anti-nuclear antibody titers measured using rat hepatocytes, were normal, and renal biopsy showed features of microangiopathic hemolysis, fibrinoid change, patchy tubular atrophy, and concentric intimal proliferation. A clinical diagnosis of diarrhea-negative hemolytic uremic syndrome was made and she was treated with plasma exchange and fresh frozen plasma infusion. However, she remained dialysis-dependent. Several weeks later she died following a cardiac arrest. Post-mortem examination revealed medial hypertrophy, concentric intimal proliferation, and thrombi within the small arteries of the kidneys and lungs. Subsequent results from tests taken at the time of her presentation with acute renal failure revealed a normal von Willebrand factor qualitative distribution, and a positive anti-nuclear antibody titer (using a human cell line) in association with positive autoantibodies to RNA polymerase types I, II, and III. Taken together, the clinical, laboratory, and post-mortem findings were suggestive of a diagnosis of systemic sclerosis. We discuss the differential diagnoses, and the associations between these and malignancy and chemotherapy. Finally, we consider the serological tests used for the diagnosis of systemic sclerosis that were, in this case, initially misleading.

摘要

急性肾衰竭伴微血管病性溶血性贫血以及血栓性微血管病的病理表现可能出现在多种病症中,包括溶血性尿毒症综合征、血栓性血小板减少性紫癜和系统性硬化症。基于临床依据区分这些病症可能很困难,进一步的检查,包括血清学检测,通常会有所帮助。我们报告一名患者,她因IIb期卵巢癌接受了5个周期的每月一次卡铂化疗,随后出现急性肾衰竭、微血管病性溶血以及一些系统性硬化症的皮肤特征。初始血清学检测,包括使用大鼠肝细胞检测的抗核抗体滴度,均正常,肾活检显示微血管病性溶血、纤维蛋白样改变、斑片状肾小管萎缩和同心性内膜增生的特征。临床诊断为腹泻阴性的溶血性尿毒症综合征,她接受了血浆置换和新鲜冰冻血浆输注治疗。然而,她仍依赖透析。几周后,她因心脏骤停死亡。尸检显示肾脏和肺部小动脉有中层肥厚、同心性内膜增生和血栓形成。她出现急性肾衰竭时的后续检测结果显示血管性血友病因子定性分布正常,抗核抗体滴度呈阳性(使用人细胞系),同时针对I、II和III型RNA聚合酶的自身抗体呈阳性。综合临床、实验室和尸检结果,提示诊断为系统性硬化症。我们讨论了鉴别诊断,以及这些病症与恶性肿瘤和化疗之间的关联。最后,我们考虑了用于诊断系统性硬化症的血清学检测,在本例中,这些检测最初产生了误导。

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