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先天性盆腔动静脉畸形伴大量前列腺出血:一例报告

Congenital pelvic arteriovenous malformation with massive prostatic hemorrhage: a case report.

作者信息

Siegelbaum M H, Samaha A M, Gerber W L, White J V, Friedman A C, Seidmon E J, Kendall A R

机构信息

Department of Urology, Temple University Health Sciences Center, Philadelphia, Pennsylvania.

出版信息

J Urol. 1989 Feb;141(2):382-4. doi: 10.1016/s0022-5347(17)40777-4.

Abstract

Congenital arteriovenous malformations in the true pelvis are extremely rare: only 7 cases have been described in male patients. We report on a patient who presented with massive hemorrhage after transrectal prostatic biopsy and transurethral resection of the prostate. Diagnosis was established by means of magnetic resonance imaging and confirmed by arteriography. Our attempt at management by embolization and subsequent surgical ligation is described. A literature review and discussion of arteriovenous anomalies are presented.

摘要

真性骨盆内的先天性动静脉畸形极为罕见

仅7例男性患者的病例被报道过。我们报告了1例经直肠前列腺活检和经尿道前列腺切除术后出现大出血的患者。通过磁共振成像确诊,并经动脉造影证实。描述了我们通过栓塞及随后的手术结扎进行治疗的尝试。并对动静脉畸形进行了文献综述和讨论。

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