Decision-making in pediatric persistent Mullerian duct syndrome
Autor: | Ismael Nassar, Ameer Al-Hadidi, Ahmad Shaltaf, Nathan M. Novotny, Wael Amro |
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Rok vydání: | 2018 |
Předmět: |
Gynecology
endocrine system medicine.medical_specialty medicine.diagnostic_test urogenital system business.industry Uterus 030209 endocrinology & metabolism cryptorchidism Mullerian duct syndrome male pseudohermaphroditism undescended testicle medicine.disease Undescended testicle 03 medical and health sciences 0302 clinical medicine Bilateral Cryptorchidism medicine.anatomical_structure 030220 oncology & carcinogenesis Pediatrics Perinatology and Child Health Persistent Müllerian duct syndrome Male pseudohermaphroditism Biopsy Medicine Surgery business Laparoscopy Duct (anatomy) |
Zdroj: | Annals of Pediatric Surgery; Vol 14, No 1 (2018); 24-26 |
ISSN: | 1687-4137 |
DOI: | 10.1097/01.xps.0000508441.14233.56 |
Popis: | We are reporting a case of an 18-month old male who presented with bilateral cryptorchidism. The patient underwent an explorative laparoscopy in which two gonads were identified in close proximity to the uterus and fallopian tubes. Biopsy of the gonads confirmed testicular tissue. Genetic analysis demonstrated a 46, XY male. Male external genitalia were appropriate for age with no evidence of female structures. Persistent Mullerian duct syndrome is extremely rare, with approximately 260 cases reported in the literature. Best practice for the extent of surgical management is still evolving as we gather data on long-term outcome Keywords: cryptorchidism, Mullerian duct syndrome, male pseudohermaphroditism, undescended testicle |
Databáze: | OpenAIRE |
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