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[A case of persistent Mullerian duct syndrome diagnosed by laparoscopic examination for impalpable testis].
Hinyokika Kiyo. 2012 Sep; 58(9):507-9.HK

Abstract

Persistent mullerian duct syndrome describes a group of patients with a 46 XY karyotype and normal male external genitalia, but internal mullerian structures. A 7-month-old boy presented with a left inguinal hernia, a left undescended testis and a right impalpable testis. Inguinal herniorrhaphy was performed and laparoscopy was done for search of a right impalpable testis and internal genitalia simultaneously. Laparoscopic examination revealed the structure like a mullerian duct remnant along the left spermatic duct in rectovesical fossa and right intra-abdominal testis. The structure like a mullerian duct remnant was not removed to preserve the left spermatic duct. Left orchiopexy and right laparoscopic staged Fowler- Stephens orchiopexy were performed. Chromosomal analysis was 46 XY karyotype and we diagnosed this case as persistent mullerian duct syndrome.

Authors+Show Affiliations

The Department of Urology, Nara Medical University, Japan.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

jpn

PubMed ID

23070392

Citation

Goto, Daisuke, et al. "[A Case of Persistent Mullerian Duct Syndrome Diagnosed By Laparoscopic Examination for Impalpable Testis]." Hinyokika Kiyo. Acta Urologica Japonica, vol. 58, no. 9, 2012, pp. 507-9.
Goto D, Aoki K, Otsuka K, et al. [A case of persistent Mullerian duct syndrome diagnosed by laparoscopic examination for impalpable testis]. Hinyokika Kiyo. 2012;58(9):507-9.
Goto, D., Aoki, K., Otsuka, K., Kuwada, M., Yoshida, K., Fujimoto, K., & Hirao, Y. (2012). [A case of persistent Mullerian duct syndrome diagnosed by laparoscopic examination for impalpable testis]. Hinyokika Kiyo. Acta Urologica Japonica, 58(9), 507-9.
Goto D, et al. [A Case of Persistent Mullerian Duct Syndrome Diagnosed By Laparoscopic Examination for Impalpable Testis]. Hinyokika Kiyo. 2012;58(9):507-9. PubMed PMID: 23070392.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [A case of persistent Mullerian duct syndrome diagnosed by laparoscopic examination for impalpable testis]. AU - Goto,Daisuke, AU - Aoki,Katsuya, AU - Otsuka,Kenji, AU - Kuwada,Masaomi, AU - Yoshida,Katsunori, AU - Fujimoto,Kiyohide, AU - Hirao,Yoshihiko, PY - 2012/10/17/entrez PY - 2012/10/17/pubmed PY - 2012/12/21/medline SP - 507 EP - 9 JF - Hinyokika kiyo. Acta urologica Japonica JO - Hinyokika Kiyo VL - 58 IS - 9 N2 - Persistent mullerian duct syndrome describes a group of patients with a 46 XY karyotype and normal male external genitalia, but internal mullerian structures. A 7-month-old boy presented with a left inguinal hernia, a left undescended testis and a right impalpable testis. Inguinal herniorrhaphy was performed and laparoscopy was done for search of a right impalpable testis and internal genitalia simultaneously. Laparoscopic examination revealed the structure like a mullerian duct remnant along the left spermatic duct in rectovesical fossa and right intra-abdominal testis. The structure like a mullerian duct remnant was not removed to preserve the left spermatic duct. Left orchiopexy and right laparoscopic staged Fowler- Stephens orchiopexy were performed. Chromosomal analysis was 46 XY karyotype and we diagnosed this case as persistent mullerian duct syndrome. SN - 0018-1994 UR - https://www.unboundmedicine.com/medline/citation/23070392/[A_case_of_persistent_Mullerian_duct_syndrome_diagnosed_by_laparoscopic_examination_for_impalpable_testis]_ L2 - https://repository.kulib.kyoto-u.ac.jp/dspace/handle/2433/160114 DB - PRIME DP - Unbound Medicine ER -