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Surgical correction of buried penis: a review of 60 cases.

Identifieur interne : 000556 ( Ncbi/Curation ); précédent : 000555; suivant : 000557

Surgical correction of buried penis: a review of 60 cases.

Auteurs : J H Chuang [Taïwan] ; L Y Chen ; C S Shieh ; S Y Lee

Source :

RBID : pubmed:11226988

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English descriptors

Abstract

The authors reviewed 60 cases of buried penis, treated in a single institution with postoperative follow-up for at least 6 months. The review was aimed at providing information that might help to optimize the results in future surgical correction of this uncommon, but not rare, congenital disorder.

DOI: 10.1053/jpsu.2001.21606
PubMed: 11226988

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pubmed:11226988

Le document en format XML

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<nlm:affiliation>Department of Pediatric Surgery, Chang Gung Children's Hospital at Kaohsiung, Taiwan.</nlm:affiliation>
<country xml:lang="fr">Taïwan</country>
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<name sortKey="Chen, L Y" sort="Chen, L Y" uniqKey="Chen L" first="L Y" last="Chen">L Y Chen</name>
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<name sortKey="Shieh, C S" sort="Shieh, C S" uniqKey="Shieh C" first="C S" last="Shieh">C S Shieh</name>
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<name sortKey="Lee, S Y" sort="Lee, S Y" uniqKey="Lee S" first="S Y" last="Lee">S Y Lee</name>
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<term>Penile Diseases (complications)</term>
<term>Penile Diseases (congenital)</term>
<term>Penile Diseases (surgery)</term>
<term>Phimosis (etiology)</term>
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<term>Complications postopératoires</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
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<term>Maladies du pénis ()</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Phimosis ()</term>
<term>Phimosis (étiologie)</term>
<term>Procédures de chirurgie urologique masculine ()</term>
<term>Réintervention</term>
<term>Techniques de suture</term>
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<term>Penile Diseases</term>
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<term>Penile Diseases</term>
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<term>Phimosis</term>
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<term>Penile Diseases</term>
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<term>Phimosis</term>
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<term>Nourrisson</term>
<term>Phimosis</term>
<term>Procédures de chirurgie urologique masculine</term>
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<front>
<div type="abstract" xml:lang="en">The authors reviewed 60 cases of buried penis, treated in a single institution with postoperative follow-up for at least 6 months. The review was aimed at providing information that might help to optimize the results in future surgical correction of this uncommon, but not rare, congenital disorder.</div>
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