镰状细胞病中的阴茎异常勃起。

Priapism in sickle cell disease.

作者信息

Gradisek R E

出版信息

Ann Emerg Med. 1983 Aug;12(8):510-2. doi: 10.1016/s0196-0644(83)80651-9.

Abstract

An 18-year-old black man with known history of homozygous (SS) sickle cell disease presented with sudden onset of priapism awakening him from sleep. Priapism as an isolated manifestation, without other signs or symptoms of sickle cell crisis, is thought to be more prevalent than previously reported. The patient was taken to surgery, where 14-gauge intercaths were used to aspirate blood from his corpora cavernosa bilaterally. Complete detumescence was achieved. At a five-month follow-up visit, normal erectile capacity was reported.

摘要

一名18岁的黑人男性，已知患有纯合子（SS）镰状细胞病，因阴茎异常勃起突然发作而从睡眠中惊醒前来就诊。阴茎异常勃起作为一种孤立的表现，没有镰状细胞危象的其他体征或症状，被认为比之前报道的更为普遍。该患者接受了手术，术中使用14号静脉内导管从双侧海绵体抽血。阴茎完全消肿。在五个月的随访中，报告显示勃起功能正常。