<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11</volume><submitter>Huang H</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Ectopic scrotum (ES) is an extremely rare congenital scrotal malformation. Ectopic scrotum with VATER/VACTERL [vertebral defects (V), anal atresia or anorectal malformations (A), cardiac defects (C), tracheoesophageal fistula with or without esophageal atresia (TE), cardiac defects, renal malformations (R), and limb defects (L)] association is even rarer. There are no uniform guidelines for diagnosis and treatment.&lt;h4>Clinical case&lt;/h4>We described a 2-year-5-month-old boy who has ectopic scrotum and penoscrotal transposition and reviewed relevant literature in this report. We performed laparoscopy exploration, rotation flap scrotoplasty, and orchiopexy and achieved a great result during the postoperative follow-up.&lt;h4>Conclusions&lt;/h4>Combined with the previous literatur</pubmed_abstract><journal>Frontiers in pediatrics</journal><pagination>1015384</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9989158</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Ectopic scrotum and penoscrotal transposition: Case report and literature review.</pubmed_title><pmcid>PMC9989158</pmcid><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Yang H</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Huang H</pubmed_authors><pubmed_authors>Lin J</pubmed_authors><pubmed_authors>Xu Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ectopic scrotum and penoscrotal transposition: Case report and literature review.</name><description>&lt;h4>Background&lt;/h4>Ectopic scrotum (ES) is an extremely rare congenital scrotal malformation. Ectopic scrotum with VATER/VACTERL [vertebral defects (V), anal atresia or anorectal malformations (A), cardiac defects (C), tracheoesophageal fistula with or without esophageal atresia (TE), cardiac defects, renal malformations (R), and limb defects (L)] association is even rarer. There are no uniform guidelines for diagnosis and treatment.&lt;h4>Clinical case&lt;/h4>We described a 2-year-5-month-old boy who has ectopic scrotum and penoscrotal transposition and reviewed relevant literature in this report. We performed laparoscopy exploration, rotation flap scrotoplasty, and orchiopexy and achieved a great result during the postoperative follow-up.&lt;h4>Conclusions&lt;/h4>Combined with the previous literatur</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-05T14:16:44.841Z</modification><creation>2025-02-19T04:44:04.809Z</creation></dates><accession>S-EPMC9989158</accession><cross_references><pubmed>36896407</pubmed><doi>10.3389/fped.2023.1015384</doi></cross_references></HashMap>