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Type 2 transverse testicular ectopia: A case report.

F Bchini1, M Boughdir1, A Daib1

  • 1Pediatric Surgery Department, Hospital Habib Thameur, Tunis, Tunisia.

Urology Case Reports
|November 8, 2021
PubMed
Summary
This summary is machine-generated.

Transverse testicular ectopia (TTE) is a rare condition where both testes are found in one hemiscrotum. This case report details the surgical management of TTE in an infant, including addressing a persistent Mullerian duct.

Keywords:
Nonpalpable testisPersistent mullerian duct syndromeSurgeryTransverse testicular ectopia

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Area of Science:

  • Pediatric Surgery
  • Developmental Biology
  • Urology

Background:

  • Transverse testicular ectopia (TTE) is a rare congenital anomaly characterized by bilateral testes residing in a single hemiscrotum or inguinal canal.
  • Surgical intervention is the primary treatment modality for TTE.

Observation:

  • A case of type 2 TTE is presented in an 8-month-old male infant.
  • The patient presented with a right inguinal hernia and a non-palpable left testis.
  • Ultrasonography revealed both testes located in the right inguinal region.

Findings:

  • The patient's condition was associated with persistent Mullerian duct (PMD).
  • Surgical management involved the excision of the Mullerian duct remnant.
  • Bilateral orchiopexy was successfully performed to correct the testicular position.

Implications:

  • This case highlights the importance of thorough diagnostic evaluation in TTE cases, including assessment for associated anomalies like PMD.
  • Successful surgical correction of TTE and PMD in infants can lead to favorable outcomes.
  • Management strategies for TTE and associated Mullerian duct anomalies require specialized pediatric surgical expertise.