Persistent Mullerian duct syndrome

D. E.E. Rizk; M. Ezimokhai; A. S. Hussein; S. Gerami; P. Deb

doi:10.1007/s004040050208

Persistent Mullerian duct syndrome

D. E.E. Rizk, M. Ezimokhai, A. S. Hussein, S. Gerami, P. Deb

Research output: Contribution to journal › Article › peer-review

9 Citations (Scopus)

Abstract

We report an 18-month old male presenting with a right-sided inguinal hernia and undescended testes. At herniotomy, a uterus and two fallopian tubes were found in the pelvic peritoneum adjacent to the two gonads which received their blood supply paltry along the Mullerian duct remnants. The gonads were testes by histological examination. Bilateial orchiopexy was performed without removal of the Mullerian structures for fear of jeopardizing the testicular blood supply. The diagnosis of persistent Mullerian duct syndrome was confirmed postoperatively by genetic and hormonal investigations.

Original language	English
Pages (from-to)	105-107
Number of pages	3
Journal	Archives of Gynecology and Obstetrics
Volume	261
Issue number	2
DOIs	https://doi.org/10.1007/s004040050208
Publication status	Published - 1998
Externally published	Yes

Keywords

Cryptorchidism
Inguinal hernia
Persistent Mullerian duct syndrome
Undescended testis
Uterine hernia syndrome

ASJC Scopus subject areas

Obstetrics and Gynaecology

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10.1007/s004040050208

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title = "Persistent Mullerian duct syndrome",

abstract = "We report an 18-month old male presenting with a right-sided inguinal hernia and undescended testes. At herniotomy, a uterus and two fallopian tubes were found in the pelvic peritoneum adjacent to the two gonads which received their blood supply paltry along the Mullerian duct remnants. The gonads were testes by histological examination. Bilateial orchiopexy was performed without removal of the Mullerian structures for fear of jeopardizing the testicular blood supply. The diagnosis of persistent Mullerian duct syndrome was confirmed postoperatively by genetic and hormonal investigations.",

keywords = "Cryptorchidism, Inguinal hernia, Persistent Mullerian duct syndrome, Undescended testis, Uterine hernia syndrome",

author = "Rizk, {D. E.E.} and M. Ezimokhai and Hussein, {A. S.} and S. Gerami and P. Deb",

year = "1998",

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T1 - Persistent Mullerian duct syndrome

AU - Rizk, D. E.E.

AU - Ezimokhai, M.

AU - Hussein, A. S.

AU - Gerami, S.

AU - Deb, P.

PY - 1998

Y1 - 1998

N2 - We report an 18-month old male presenting with a right-sided inguinal hernia and undescended testes. At herniotomy, a uterus and two fallopian tubes were found in the pelvic peritoneum adjacent to the two gonads which received their blood supply paltry along the Mullerian duct remnants. The gonads were testes by histological examination. Bilateial orchiopexy was performed without removal of the Mullerian structures for fear of jeopardizing the testicular blood supply. The diagnosis of persistent Mullerian duct syndrome was confirmed postoperatively by genetic and hormonal investigations.

AB - We report an 18-month old male presenting with a right-sided inguinal hernia and undescended testes. At herniotomy, a uterus and two fallopian tubes were found in the pelvic peritoneum adjacent to the two gonads which received their blood supply paltry along the Mullerian duct remnants. The gonads were testes by histological examination. Bilateial orchiopexy was performed without removal of the Mullerian structures for fear of jeopardizing the testicular blood supply. The diagnosis of persistent Mullerian duct syndrome was confirmed postoperatively by genetic and hormonal investigations.

KW - Cryptorchidism

KW - Inguinal hernia

KW - Persistent Mullerian duct syndrome

KW - Undescended testis

KW - Uterine hernia syndrome

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JO - Archives of Gynecology and Obstetrics

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Persistent Mullerian duct syndrome

Abstract

Keywords

ASJC Scopus subject areas

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