Congenital bilateral scrotal agenesis with bilateral cryptorchidism: a case report

Authors

  • Ram Jeewan Singh Department of Pediatric Surgery, All India Institute of Medical Sciences, Patna, Bihar, India
  • Bijay Kumar Suman Department of Pediatric Surgery, All India Institute of Medical Sciences, Patna, Bihar, India
  • Keerthana Bachala Department of Pediatric Surgery, All India Institute of Medical Sciences, Patna, Bihar, India
  • Amit Kumar Sinha Department of Pediatric Surgery, All India Institute of Medical Sciences, Patna, Bihar, India
  • Bindey Kumar Department of Pediatric Surgery, All India Institute of Medical Sciences, Patna, Bihar, India

DOI:

https://doi.org/10.18203/2349-3291.ijcp20231155

Keywords:

Cryptorchidism, Dihydrotestosterone, Scrotal agenesis, Testosterone

Abstract

Congenital bilateral scrotal agenesis is very rare anomaly and characterized by the absence of scrotal rugae. It may be associated with other extra-genital anomalies as a part of a syndrome. Etiology is unknown but may be due to primary failure of labioscrotal folds development or secondary to localized 5-alpha-reductase type 2 deficiency. Various surgical techniques used for neoscrotum construction with different types of complications. In index case, we performed bilateral orchidopexy without creating neoscrotum.

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Published

2023-04-27

Issue

Section

Case Reports