Polycystic Kidney Disease Accompanied by Unilateral Renal Agenesis and Ulcerative Colitis: Case Report

2012 ◽  
Vol 32 (6) ◽  
pp. 1770-1772
Author(s):  
Mahir CENGİZ ◽  
Alper DÖVENTAŞ ◽  
Aslı ÇURGUNLU ◽  
Erkan YILDIRIM ◽  
Deniz Suna ERDİNÇLER ◽  
...  
Keyword(s):  
Ulcerative Colitis ◽  
Case Report ◽  
Kidney Disease ◽  
Polycystic Kidney Disease ◽  
Renal Agenesis ◽  
Polycystic Kidney ◽  
Unilateral Renal Agenesis

scholarly journals Unilateral Autosomal Dominant Polycystic Kidney Disease with Contralateral Renal Agenesis: A Case Report

2003 ◽  
Vol 18 (2) ◽  
pp. 284 ◽  
Author(s):  
Gyun Ho Jeong ◽  
Byoung Seok Park ◽  
Taek Kyun Jeong ◽  
Seong Kwon Ma ◽  
Chung Ho Yeum ◽  
...  
Keyword(s):  
Case Report ◽  
Kidney Disease ◽  
Polycystic Kidney Disease ◽  
Autosomal Dominant ◽  
Renal Agenesis ◽  
Polycystic Kidney ◽  
Autosomal Dominant Polycystic Kidney

scholarly journals Use of Eculizumab in Transplant-Associated Thrombotic Microangiopathy in a Patient With Polycystic Kidney Disease Immediately Post–Kidney Transplant: A Case Report

2020 ◽  
Vol 2 (5) ◽  
pp. 652-656 ◽  
Author(s):  
Amandeep Godara ◽  
Daniel R. Migliozzi ◽  
Monika Pilichowska ◽  
Nitender Goyal ◽  
Cindy Varga ◽  
...  
Keyword(s):  
Case Report ◽  
Kidney Disease ◽  
Kidney Transplant ◽  
Polycystic Kidney Disease ◽  
Thrombotic Microangiopathy ◽  
Polycystic Kidney

scholarly journals Spontaneous coronary artery dissection in a patient with hereditary polycystic kidney disease and a recent liver transplant: a case report

2019 ◽  
Vol 3 (4) ◽  
pp. 1-5 ◽  
Author(s):  
Ezther Verlaeckt ◽  
Laurens Van de Bruaene ◽  
Mathieu Coeman ◽  
Sofie Gevaert
Keyword(s):  
Case Report ◽  
Coronary Artery ◽  
Kidney Disease ◽  
Liver Transplant ◽  
Polycystic Kidney Disease ◽  
Artery Dissection ◽  
High Dose ◽  
Spontaneous Coronary Artery Dissection ◽  
Polycystic Kidney ◽  
Coronary Artery Dissection

Abstract Background Spontaneous coronary artery dissection (SCAD) is an underestimated cause of acute coronary syndromes. A predisposing arteriopathy is often present and a stressor can sometimes be identified. Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disorder; its associated arteriopathy has been described as a predisposing condition for SCAD. Case summary A 44-year-old woman with ADPKD presented in the emergency room with recent onset thoracic pain radiating to the left arm at rest. She had undergone a recent liver transplant, for which she had received high-dose corticosteroids during 1 month. She was still taking tacrolimus and mycophenolate mofetil. She had no traditional risk factors but had experienced stress postoperatively. She was known with moderate chronic kidney disease. The initial electrocardiogram (ECG) was normal but high-sensitive troponin T was significantly elevated. Coronary angiography demonstrated diffuse narrowing of the distal left anterior descending artery with preserved flow, compatible with a SCAD Type 2 that was treated conservatively. However, under dual antiplatelet therapy (DAPT) with clopidogrel, the coronary dissection was progressive with new ischaemic ECG changes, further rise of troponins and development of apicoseptal hypokinesia. Because of the small vessel diameter and the preserved distal flow, conservative treatment was maintained. Clopidogrel was interrupted and the patient remained stable. Discussion As SCAD remains an underestimated cause of myocardial infarction, clinicians should be aware of the possibility of SCAD in ADPKD patients with chest pain. This case report illustrates that the decision DAPT vs. aspirin should be individualized in these patients.

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