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BSMMU 肾内科收治的一位发生灾难性抗磷脂综合征的中年女性

A Middle-Aged Woman Presented with Catastrophic Anti-phospholipid Syndrome in Nephrology Department of BSMMU.

机构信息

Dr Md Omar Faroque, Associate Professor, Department of Nephrology, Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka, Bangladesh; E-mail:

出版信息

Mymensingh Med J. 2022 Jan;31(1):267-271.

Abstract

A life threatening rare condition called catastrophic antiphospholipid syndrome leading to multiple organ failure is characterized by vascular thrombosis in the presence of anti-phospholipid antibody which often appear as a medical emergency. Antiphospholipid antibody syndrome whether primary or secondary cause thromboembolic manifestation resulting recurrent fetal loss, but catastrophic antiphospholipid antibody syndrome may not present in such a way, rather multi-system involvement occurs within a short period of time. We would like to present a case of 50 years old female who is hypertensive, non-diabetic, a known case of hypothyroidism for two years, who was admitted to our hospital after developing fever for 7 days and black discoloration of lateral three fingers of left hand for short period of time. The patient had no medical problems and had been in her usual state of health until 7 days before admission. Patient is anaemic and found to have severe renal failure. She was found high titer antiphospholipid antibody both IgM and IgG positive and anti-cardiolipin antibody positive. Her routine investigations revealed very high neutrophilic leukocytosis, high acute phase reactant, urinary findings revealed no active sediment; we thought that our patient might have sepsis that may trigger catastrophic antiphospholipid syndrome. Multi-disciplinary consultation gave us valuable opinion. Considering her septicemia, she was given broad spectrum antibiotic. Anticoagulation was given with unfractionated heparin followed by warfarin and as an immunosuppressive protocol methylprednisolone followed by prednisolone along with pulse cyclophosphamide was given. Treatment option with plasma pheresis and monoclonal antibody was not attempted, but she was given several session of hemodialysis, within a few days her biochemical parameters improved. Severe renal failure in this patient may be explained by septicemia or thrombotic micro-angiopathy that was reversed with anti-coagulation or proper antibiotic. Amputation of three digit of left hand was done by orthopedic surgeon but unfortunately two weeks after admission the patient expired due to sudden stroke.

摘要

一种危及生命的罕见疾病称为灾难性抗磷脂综合征,可导致多器官衰竭,其特征是存在抗磷脂抗体的血管血栓形成,这种情况通常表现为医疗紧急情况。抗磷脂抗体综合征无论是原发性还是继发性,都会导致血栓栓塞表现,从而导致反复流产,但灾难性抗磷脂抗体综合征可能不会以这种方式出现,而是在短时间内多系统受累。我们想介绍一位 50 岁的女性患者,她患有高血压,非糖尿病,患有甲状腺功能减退症已有两年,在出现发热 7 天和左手外侧三个手指变黑后被收入我院。患者没有任何医疗问题,一直处于通常的健康状态,直到入院前 7 天。患者贫血,发现存在严重的肾衰竭。她被发现存在高滴度抗磷脂抗体,IgM 和 IgG 均为阳性,抗心磷脂抗体阳性。她的常规检查显示中性粒细胞白细胞增多症非常高,急性相反应物高,尿液检查无活跃沉淀物;我们认为患者可能患有败血症,可能引发灾难性抗磷脂综合征。多学科咨询为我们提供了宝贵的意见。考虑到她的败血症,给予了广谱抗生素。给予未分馏肝素抗凝治疗,随后给予华法林,作为免疫抑制方案,给予甲泼尼龙随后给予泼尼松,并给予环磷酰胺脉冲治疗。未尝试血浆置换和单克隆抗体治疗,但给予了几次血液透析,在几天内她的生化参数得到了改善。该患者的严重肾衰竭可能是由败血症或血栓性微血管病引起的,抗凝或适当的抗生素治疗可逆转。整形外科医生对左手三个手指进行了截肢,但不幸的是,入院两周后患者因突发性中风去世。

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