Congenital absence of the testis in human fetuses and in cryptorchid patients

Int J Urol. 2004 Dec;11(12):1110-3. doi: 10.1111/j.1442-2042.2004.00952.x.

Abstract

Background: The aim of the present study is to make a comparative study in human fetuses and in patients with cryptorchidism, analyzing the incidence of a number anomalies of the testes for both populations.

Methods: We studied 326 testes from 163 human fetuses ranging in age from 10 to 35 weeks postconception (WPC) and 133 testes from 101 cryptorchid patients aged from 1 to 15 years old (mean, 6.4 years). The Fisher's exact test was used for comparison.

Results: Among 326 fetal testes, 224 (68.7%) were abdominal, 45 (13.8%) were inguinal and 55 (16.8%) were scrotal. In one fetus at 23 WPC, both testes (0.6%) were absent. Of the 133 cryptorchid testes, 17 (12.78%) were abdominal, 92 (69.1%) were inguinal and 24 (18%) were high scrotal. Of the 17 abdominal testes, three (17.6%) were atrophic and two were vanished (11.7%). Of the 92 inguinal testes, one (1.08%) was vanished. Twenty-eight (21%) of the cryptorchid testes were impalpable and among these, 17 were located in the abdomen (60.7%) and 11 (38.2%) in the inguinal region (internal ring).

Conclusions: Testicular agenesis is a very rare anomaly, both in fetuses and patients with cryptorchidism.

Publication types

  • Comparative Study

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Cryptorchidism / complications
  • Cryptorchidism / embryology
  • Cryptorchidism / pathology*
  • Fetus
  • Gestational Age
  • Humans
  • Incidence
  • Infant
  • Inguinal Canal / pathology
  • Male
  • Scrotum / pathology
  • Testis / abnormalities*
  • Testis / embryology