Evidence map›Paper›PMID 35434100›Full record

ArticleWorld journal of clinical cases2022

Bilateral ureteral reimplantation in a patient with an intraperitoneal ectopic bipenis: A case report.

Ya-Tao Jia, Bao-Lei Shi, Jie Zhang, Ying-Yi Li, Jiang Zhu

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In one paragraph

Article in World journal of clinical cases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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3 · Its place in the literature

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0 citing papers in PubMed, 0 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Ya-Tao JiaDepartment of Urology, Baoji People's Hospital, Baoji 721000, Shannxi Province, China.
Bao-Lei ShiDepartment of Urology, Baoji People's Hospital, Baoji 721000, Shannxi Province, China.
Jie ZhangDepartment of Urology, Baoji People's Hospital, Baoji 721000, Shannxi Province, China.
Ying-Yi LiDepartment of Urology, Baoji People's Hospital, Baoji 721000, Shannxi Province, China.
Jiang ZhuDepartment of Urology, Baoji People's Hospital, Baoji 721000, Shannxi Province, China. 104509560@qq.com.
Baoji City Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiphallia is a highly uncommon congenital urogenital abnormality and a few connected reports have been published. However, no case of intraabdominal heterotopic diphallus has been documented to date. In the present study, we present a rare case of intraperitoneal ectopic bipenis. CASE SUMMARY: A 49-year-old man was hospitalized with the chief complaint of hydronephrosis of both kidneys, which was discovered three days earlier through regular physical examination performed using urological ultrasound without significant lumbar or abdominal pain or bladder irritation. Physical examination showed normal external penile development, bilateral testes located on the left side of the scrotum, and a fused epididymis. Urological plain and enhanced computed tomography suggested bilateral hydronephrosis, bilateral ureters opened to the left side of the bladder wall; an intrapelvic soft tissue shadow on the left side of the bladder was considered a germline malformation called bipenis (hidden penis in the abdominal cavity). Based on the urological plain and enhanced computed tomography results, a 49-year-old man was diagnosed with bipenis (one hidden in the abdominal cavity). Ectopic penile compression produced bilateral ureteral dilatation and hydronephrosis. The ectopic penis was amputated and partially removed during surgery, and bilateral ureteral replantation was successfully performed. At a 2-mo follow-up, the patient was very satisfied with the operation, there was no significant hydronephrosis in both kidneys, and urination and erectile function were normal.

conclusionTo our knowledge, this is the first report of diphallia with an intraperitoneal ectopic penis. Computed tomography or magnetic resonance imaging can be used to assess the associated internal anomalies before surgery. Postoperative pathological findings are the gold standard for the diagnosis.

Indexed as

Case reportDiphalliaIntraperitoneal ectopic penisPenis duplicationUreteral reimplantation

Identifiers

PMID35434100
PMCPMC8968799
OpenAlexW4220743734

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