Suspected Pulmonary Embolism Postcesarean Section in a Patient with Autosomal Dominant Polycystic Kidney Disease.

Olusegun O Badejoko, Olufunke F Dada, Akaninyene E Ubom, Olumuyiwa T Ajayeoba
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Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetically inherited kidney disease worldwide. It is however relatively underdiagnosed in Africans because its diagnosis is often incidental. During pregnancy, ADPKD is associated with increased risk of preeclampsia and venous thromboembolism. The case of a 33-year-old lady incidentally diagnosed with ADPKD during pregnancy is presented. She developed preeclampsia at term and had cesarean delivery of twins. She however suffered cardiopulmonary arrest postoperatively and this created a treatment dilemma because therapeutic anticoagulation which was the primary treatment for her suspected pulmonary embolism was absolutely contraindicated if the actual cause of her collapse was ruptured cerebral aneurysm which was also a feature of ADPKD. We decided to resuscitate aggressively and perform an urgent cranial computed tomography which ruled out intracranial hemorrhage. We then commenced anticoagulation and she made an excellent recovery. This case illustrates the importance of a timely multidisciplinary approach to patient management.

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常染色体显性多囊肾病患者剖宫产术后疑似肺栓塞1例。
常染色体显性多囊肾病(ADPKD)是世界上最常见的遗传性肾病。然而,非洲人对该病的诊断相对较少,因为其诊断往往是偶然的。在怀孕期间,ADPKD与子痫前期和静脉血栓栓塞的风险增加有关。病例33岁的妇女偶然诊断为ADPKD在怀孕期间提出。她在足月时患上了先兆子痫,并剖宫产了一对双胞胎。然而,她术后出现了心肺骤停,这造成了治疗困境,因为治疗抗凝治疗是她疑似肺栓塞的主要治疗方法,如果她崩溃的实际原因是脑动脉瘤破裂,这也是ADPKD的一个特征,这是绝对禁忌的。我们决定积极抢救,并进行紧急颅脑电脑断层扫描,排除颅内出血的可能。然后我们开始抗凝治疗,她恢复得很好。这个病例说明了及时的多学科方法对患者管理的重要性。
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