两名原发性抗磷脂综合征（PAPS）患者肾移植后复发性肾血栓性微血管病。
Recurrent renal thrombotic angiopathy after kidney transplantation in two patients with primary antiphospholipid syndrome (PAPS).
作者信息
Mondragón-Ramírez G, Bochicchio T, García-Torres R, Amigo M C, Martínez-Lavin M, Reyes P, Herrera-Acosta J
机构信息
Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
出版信息
Clin Transplant. 1994 Apr;8(2 Pt 1):93-6.
PMID:8019028
Abstract
Renal artery and venous thrombosis and thrombotic microangiopathy have been related to PAPS. This condition may lead to end-stage renal disease (ESRD). We present 2 patients with PAPS and ESRD who received a living unrelated kidney transplant. Despite intensive anticoagulant therapy, the disease recurred in the grafts.
摘要
肾动脉和静脉血栓形成以及血栓性微血管病与抗磷脂综合征（PAPS）有关。这种情况可能导致终末期肾病（ESRD）。我们报告了2例患有抗磷脂综合征和终末期肾病并接受了非亲属活体肾移植的患者。尽管进行了强化抗凝治疗，但疾病仍在移植肾中复发。
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