@article{ajmsm20221032,
author={{Leon, Madeleidis Lopez and Abdelmoneim, Sahar S. and Leon, Milenis Lopez and Hernandez, Sandy Espinosa and Idrees, Mohsin M. and Bermudez, Francisco Lopez and Ross, Lazaro U. Suarez and Dua, Rishbha and Frontela, Odalys},
title={Recurrent Hematuria in a Patient with Autosomal Dominant Polycystic Kidney Disease (ADPKD) and Renal Transplantation: A Case Report},
journal={American Journal of Medical Sciences and Medicine},
volume={10},
number={3},
pages={78--81},
year={2022},
url={http://pubs.sciepub.com/ajmsm/10/3/2},
issn={2327-6657},
abstract={Hematuria occurrence in autosomal dominant polycystic kidney disease (ADPKD) is common and can be a manifestation of cyst bleeding. Patients with ADPKD who receive kidney transplantation can present with recurrent hematuria. Malignancy, urinary tract infections, calculus obstruction or any recent diagnostic or interventional procedures can all manifest with hematuria. Knowledge of the precipitating factors and clinical presentation in those patients will help practicing internists in performing an appropriate evaluation and management of these entities and their complications, as well as execute a timely referral to subspecialists for native kidney nephrectomies when indicated. We herein, present a case of 72-years-old female, with APKD who received kidney transplantation 14 years ago, presenting with repeated hospital admissions with flank pain and recurrent hematuria. She had experienced multiple admissions with hematuria, most likely caused by native kidney recurrent cyst bleedings.},
doi={10.12691/ajmsm-10-3-2}
publisher={Science and Education Publishing}
}