Results 151 to 160 of about 824 (195)

Transverse testicular ectopia: a rare presentation with persistent Müllerian duct syndrome. [PDF]

open access: yesJ Clin Res Pediatr Endocrinol, 2014
Telli O   +4 more
europepmc   +1 more source
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Transverse testicular ectopia

Journal of Pediatric Surgery, 1982
In transverse or crossed testicular ectopia, the affected gonad lies in the same canal as the normally descended testis. During a 5-yr span, three children with this form of ectopia were seen. All presented with a symptomatic right inguinal hernia and an empty scrotum on the left side. The ages at operation were 1, 3, and 5 mo.
M W, Gauderer   +4 more
exaly   +6 more sources

Transverse testicular ectopia with persistent müllerian duct syndrome

Journal of Pediatric Surgery, 1997
Transverse testicular ectopia is rarely associated with persistent müllerian duct syndrome. The ninth pediatric case of transverse testicular ectopia with persistent müllerian duct syndrome is reported. The clinical and operative findings and treatment are discussed.
I, Karnak   +3 more
openaire   +4 more sources

Transverse testicular ectopia

Pediatrics International, 2014
AbstractDescribed herein are six cases of transverse testicular ectopia. All patients who underwent orchidopexy at the one pediatric surgical unit between October 2001 and January 2008 were evaluated. The medical records of all patients diagnosed with transverse testicular ectopia were evaluated retrospectively. Five patients (84%) were admitted with a
Oral, Akgün   +3 more
openaire   +3 more sources

Infantile scrotal hemangioma with transverse testicular ectopia

Pediatric Dermatology, 2021
AbstractTransverse testicular ectopia is a rare structural anomaly of abnormal testicular descent. We report a case of a 3‐month‐old boy with hemiscrotal infantile hemangioma and contralateral transverse testicular ectopia.
Haley Sherburne   +4 more
openaire   +2 more sources

Transverse testicular ectopia

Journal of Pediatric Surgery, 1989
In transverse testicular ectopia, both testes are present in the same hemiscrotum. We report such a case and review the possible mechanism of this anomaly, the differential diagnosis, recognition, and management.
openaire   +2 more sources

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