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Priapism in a patient with sickle cell trait using marijuana
  1. Abhishek Matta1,2,
  2. Pavan Kumar Tandra3,4,
  3. Lyudmyla Berim5
  1. 1Department of Internal Medicine, Creighton University Medical Center, Omaha, Nebraska, USA
  2. 2Department of Internal Medicine, Veterans’ Affairs Medical Center, Omaha, Nebraska, USA
  3. 3Department of Hematology-Oncology, University of Nebraska Medical Center, Omaha, Nebraska, USA
  4. 4Department of Hematology-Oncology, Veterans’ Affairs Medical Center, Omaha, Nebraska, USA
  5. 5Department of Hematology-Oncology, Creighton University Medical Center, Omaha, Nebraska, USA
  1. Correspondence to Dr Abhishek Matta, mtarun2006{at}


A 22-year-old man with a history of multiple episodes of priapism presented to the emergency room with an erection lasting more than 48 h after conservative management failed at home. He had no known family history of sickle cell disease or trait. He was haemodynamically stable. Physical examination revealed an enlarged, tender penis. Laboratory data revealed a positive sickle solubility test. Haemoglobin electrophoresis revealed sickle cell trait and urine drug screen was positive for cannabinoids. Initial management was attempted with intracavernosal phenylephrine without any success. The patient underwent a limited El-Ghorab procedure on the right corpora cavernosa but the priapism did not resolve adequately. Two  days later, the patient had to undergo a bilateral El-Ghorab procedure and achieved complete resolution of the priapism.

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