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[Persistent Müllerian duct syndrome diagnosed by laparoscopic examination: a case report].
Hinyokika Kiyo. 2008 Jan; 54(1):35-7.HK

Abstract

A 2-year-old boy presented for the evaluation of left nonpalpable testis. Laparoscopic examination revealed right migratory testis without any abnormal appearance and a uterine-like structure with an immature gonad in rectovesical fossa. Right spermatic duct merged into the uterine-like structure on the right side. The immature gonad was removed by laparoscopic procedure, while the uterine-like structure was not removed to preserve the right spermatic duct. Right orchidopexy was also performed. Histopathologic diagnosis for the removed gonad was hypoplastic testis. After the chromosomal analysis, 46 XY karyotype, we diagnosed this case as persistent Müllerian duct syndrome. Persistent Müllerian duct syndrome diagnosed by laparoscopic examination is very rare. To the best of our knowledge, this is the third case in Japan.

Authors+Show Affiliations

Department of Urology, Hirosaki University Graduate School of Medicine.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

English Abstract
Journal Article

Language

jpn

PubMed ID

18260358

Citation

Ishimura, Hirofumi, et al. "[Persistent Müllerian Duct Syndrome Diagnosed By Laparoscopic Examination: a Case Report]." Hinyokika Kiyo. Acta Urologica Japonica, vol. 54, no. 1, 2008, pp. 35-7.
Ishimura H, Okamoto A, Imai A, et al. [Persistent Müllerian duct syndrome diagnosed by laparoscopic examination: a case report]. Hinyokika Kiyo. 2008;54(1):35-7.
Ishimura, H., Okamoto, A., Imai, A., Iwabuchi, I., Yoneyama, T., Koie, T., Yamato, T., Kamimura, N., Narita, S., & Ohyama, C. (2008). [Persistent Müllerian duct syndrome diagnosed by laparoscopic examination: a case report]. Hinyokika Kiyo. Acta Urologica Japonica, 54(1), 35-7.
Ishimura H, et al. [Persistent Müllerian Duct Syndrome Diagnosed By Laparoscopic Examination: a Case Report]. Hinyokika Kiyo. 2008;54(1):35-7. PubMed PMID: 18260358.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Persistent Müllerian duct syndrome diagnosed by laparoscopic examination: a case report]. AU - Ishimura,Hirofumi, AU - Okamoto,Akiko, AU - Imai,Atsushi, AU - Iwabuchi,Ikuya, AU - Yoneyama,Takahiro, AU - Koie,Takuya, AU - Yamato,Takashi, AU - Kamimura,Noritaka, AU - Narita,Satoshi, AU - Ohyama,Chikara, PY - 2008/2/12/pubmed PY - 2008/4/2/medline PY - 2008/2/12/entrez SP - 35 EP - 7 JF - Hinyokika kiyo. Acta urologica Japonica JO - Hinyokika Kiyo VL - 54 IS - 1 N2 - A 2-year-old boy presented for the evaluation of left nonpalpable testis. Laparoscopic examination revealed right migratory testis without any abnormal appearance and a uterine-like structure with an immature gonad in rectovesical fossa. Right spermatic duct merged into the uterine-like structure on the right side. The immature gonad was removed by laparoscopic procedure, while the uterine-like structure was not removed to preserve the right spermatic duct. Right orchidopexy was also performed. Histopathologic diagnosis for the removed gonad was hypoplastic testis. After the chromosomal analysis, 46 XY karyotype, we diagnosed this case as persistent Müllerian duct syndrome. Persistent Müllerian duct syndrome diagnosed by laparoscopic examination is very rare. To the best of our knowledge, this is the third case in Japan. SN - 0018-1994 UR - https://www.unboundmedicine.com/medline/citation/18260358/[Persistent_Müllerian_duct_syndrome_diagnosed_by_laparoscopic_examination:_a_case_report]_ L2 - https://repository.kulib.kyoto-u.ac.jp/dspace/handle/2433/71569 DB - PRIME DP - Unbound Medicine ER -