symptomatic mullerian duct cysts are uncommon. a young adult male presented to us with a palpable supra-pubic mass, pain and lower urinary tract symptoms. initial imaging modalities showed a large cystic lesion in the pelvis with a non-visualized right kidney. a short, blind ending right ureter on retrograde pyelography added to the confusion. on exploration, the lesion was noted to be separate...

BACKGROUND The anti-mullerian hormone (AMH) is a member of the transforming growth factor β (TGF-β) superfamily, which is responsible of the regression of the mullerian duct. AMH is expressed in the normal endometrium, where, acting in a paracrine fashion, negatively regulates cellular viability. Our objective was to evaluate the in vitro effects of the treatment with AMH of endometriosic cells...

BACKGROUND: Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare disorder described as aplasia or hypoplasia of uterus and vagina due to an early arrest in the development Mullerian ducts. The etiology MRKH remains uncertain: Although at beginning, it was mentioned that this result sporadic abnormalities. It has recently been assumed genetic background cause increasing number familial cases...

The female reproductive tract organs of mammals, including the oviducts, uterus, cervix and upper vagina, are derived from the Müllerian ducts, a pair of epithelial tubes that form within the mesonephroi. The Müllerian ducts form in a rostral to caudal manner, guided by and dependent on the Wolffian ducts that have already formed. Experimental embryological studies indicate that caudal elongati...

OBJECTIVES/HYPOTHESIS This study aimed to investigate the diagnosis and management of a distinct developmental deformity syndrome characterized by congenital cheek fistula, ectopic accessory parotid gland, and preauricular appendage. STUDY DESIGN Retrospective study. METHODS We analyzed the medical records, radiologic and histopathologic findings, and follow-up data for seven patients (four...

a:1:{i:0;s:867:"Cystic lesions in midline of prostate are uncommon and considered as congenital disorders. Here we report a 33- year- old male who presented with either azoospermia or decreased ejaculate volume leading to infertility and for whom performing Transrectal ultrasonography had a critical role in diagnosis. The obtained images revealed a congenital cyst of the prostate gland just in ...

Keywords: Polycystic ovarian syndrome PCOS Anti-mullerian hormone AMH PCOD Original Article Polycystic ovarian syndrome is a complex heterogeneous disorder of unknown etiology and shows mild to severe degree of signs and symptoms affecting the reproductive, endocrine and metabolic functions. Anti-mullerian hormone, a dimeric glycoprotein belonging to the transforming growth factor–beta superfam...

Syndromatic paucity of interlobular bile ducts is a common cause of conjugated hyperbilirubinemia in children. The clinical presentation is not always obvious. Therefore, the liver biopsy may be a useful diagnostic tool in the definition of this entity. The hepatic and biliary morphology of five children with arteriohepatic dysplasia (Allagille' syndrome) is described. Prior to diagnosis, four ...

•Two cases of large cervical mullerian adenosarcoma with sarcomatous overgrowth or heterologous elements and contrasting survival outcomes are reported.•When the diagnosis of mullerian adenosarcoma is uncertain or suspected, review of pathology by a national expert may be considered.•Rhabdomyoblastic differentiation of mullerian adenosarcoma may be a more aggressive histologic type.