A 26 years old lady presented to us with primary amenorrhoea. On examination and investigation she was found to have MRKH syndrome with Situs inversus totalis. Likewise what we do for these syndromic patients, we did sigmoid vaginoplasty. This is one of the uncommon anatomical variants we encountered in our series of cases. Our literature search did not reveal such patient undergoing sigmoid vaginoplasty and so is this case presented for publication.

Background: Cryptorchidism is simply defined as the absence of one or both testes from the scrotum. It is the most common birth defect of the male genitalia. The testis may be located intra-abdominal or inguinal. This article mainly deals with embryology, etiology, anatomy and incidence types of cryptorchidism in Tumakuru rural district.Methods: This study was interdepartmental and prospective, consisting of 66 cases conducted at the Department of Pediatric Surgery and Anatomy and the period of study was from April 2013- March 2017. Cryptorchidism has been classified into 1) Intra-abdominal, 2) Inguinal, 3) Ectopic testis (perineum).Results: Out of 66 cases, testis in inguinal canal is the most common incidence followed by the intra-abdominal and Ectopic testis. Least found was ectopic and torsion in the inguinal canal. Complications are torsion and vanishing testis.Conclusions: This condition is repairable in a vast majority of cases. Early diagnosis and surgical intervention have to be carried out to correct this defect.

Ovarian tumors in children and adolescents are rare. We present a case of a 15-year-old girl with mucinous cystadenoma (MCA) which was diagnosed incidentally when evaluating for anemia and reduced appetite. The scan reports suggested a large ovarian cyst with a few thick enhancing septa. Serological markers were within normal limits. She underwent a cystectomy with salpingo-oophorectomy. The cyst was reported as MCA on histopathology. The child is on regular follow-up for 6 months with no adverse events.