Mullerian adenosarcoma is a rare biphasic malignant neoplasm of the cervix characterized by an admixture of benign epithelial elements and a malignant sarcomatous stromal component, which may be either homologous or heterologous. An aggressive variant of adenosarcoma, mullerian adenosarcoma with sarcomatous overgrowth (MASO) is extremely rare, with only two such cases being reported in the Engl...

Study sample No sample size appears to have been determined in the planning phase of the study. In addition, no retrospective power calculations were reported. The authors reported that a group of MIS-TKA patients was compared with a group of 50 traditional TKA patients, but it was unclear how many patients were in the MIS-TKA group. The authors then reported that all patients (n=159) were coho...

Background. Anti-Mullerian hormone (AMH) has now gained popularity as a marker of ovarian reserve. It is important to determine the place and role AMH in children. The purpose this work was analyze data scientific literature on pediatric practice. Materials methods. A review PubMed conducted, limiting itself articles English updating search February 2022. term “anti-Mullerian hormone”. total 43...

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...

Today, infertility takes a major place in gynecology practice. Non-puerperal uterine inversion is a rare event and usually accompanies submucous myoma, leiomyosarcoma, rhabdomyosarcoma, malignant mixed Mullerian tumour, and endometrial polyp. Herein, we report a 39-year-old woman who suffered from secondary infertility together with uterine inversion, which is an extremely rare co-existence.

Persistent Mullerian Duct Syndrome (PMDS) associated with transverse testicular ectopia (TTE) is rare. Ten cases have been reported in the past. Accurate diagnosis with karyotype and histological analysis is crucial. Surgical management should be geared toward preservation of fertility when possible.