Alimentary tract duplication cysts are rare congenital anomalies, most commonly located in the ileum, but may present anywhere from mouth to anus.Clinically, they may be asymptomatic, incidentally diagnosed or may present with obstruction, volvulus, intussusception or gastrointestinal bleed. Here we report a case of a one year old male child presenting in gasping state and shock. Despite the in...

pISSN 2383-7837 eISSN 2383-7845 © 2016 The Korean Society of Pathologists/The Korean Society for Cytopathology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/ by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work...

Cutaneous endometriosis represents a non-neoplastic, ectopic growth of endometrial glands and stroma outside the uterine cavity [1-4]. Daneil Schroen, a German physician, first described endometriosis in 1690 [5]. Years later, in 1885, the first case of cutaneous endometriosis was identified and reported [3]. Cutaneous endometriosis is typically divided into two categories, scar endometriosis a...

Urachal anomalies are exceptionally rare. They can present in different ways in childhood as well as in adults. We present an interesting case of vesico-urachal diverticulum with alternating sinus. The interesting finding in this patient was the inversion and disappearance of the umbilicus at the termination of voiding

Hydatid cyst caused by Echinococcus granulosus demonstrates an endemic infection in several countries such as Middle Eastern countries. Liver is the most frequently involved organ, followed by the lung. The case we present is solitary primary localization of cyst in abdominal wall which is extremely rare. A 57-year-old woman presented with an abdominal wall lesion in umbilical area that had bee...

Variants of exstrophy are rare anomalies seen in the spectrum bladder exstrophy-epispadias complex. A seven day old male neonate was admitted our department with a variant duplicate communicating fistula. Patient presented patch exstrophic just below low set umbilicus normal sized phallus and normally positioned urethral meatus. The baby managed successfully surgery is under regular follow up.