Congenital Ilea Duplication Cyst Lined By Columnar and Squamous Epithelium: A Rare Case Report
Journal Title: Scholars Journal of Medical Case Reports - Year 2017, Vol 5, Issue 7
Abstract
Enteric duplication cysts are a rare congenital anomaly. They can occur anywhere in the gastrointestinal tract. Their most common location is the small intestine, particularly the terminal ileum. We report a rare case of a neonatal male child with intestinal duplication cyst of the ileum lined by columnar and stratified squamous epithelium.
Authors and Affiliations
Dr. Rajnish Kalra, Dr. Deepika Jain, Dr. Gurupriya J, Dr. Nitesh Kumari, Dr. Archana Budhwar, Dr. Rajeev Sen
Sodium Valproate: A Cause of Erythroderma
The antiseizure properties of the broad spectrum, non-aromatic sodium valproate are well known. It is being increasingly used in other conditions like bipolar disorders, acute mania, panic attacks and migraine. Non-aroma...
Intraparotid Schwannoma in a Young Adult: A Rare Entity
Abstract: Intraparotid schwannoma arising from facial nerve are uncommon. These are slow growing, well encapsulated tumors that may arise from the nerve sheath. Preoperative diagnosis of schwannoma is difficult due to va...
Non Traumatic Arteriovenous Fistula of the Superficial Temporal Artery
Spontaneous arteriovenous fistula (AVF) of superficial temporal artery (STA) is a very rare condition. The pathogenesis is poorly understood. The treatment may be surgical by excision or endovascular by embolization. A m...
Alobar Holoprosencephaly: about 2 cases and review of the literature
Holoprosencephaly is a rare brain abnormality resulting from an incomplete cleavage of the primitive prosencephalon of forebrain during early embryogenesis. It includes a series of rare complex and heterogenosis disorder...
A Rare Case of Chylothrax Following Surgery of Congenital Diaphragmatic Hernia
Chylothorax is a accumulation of lymphatic fluid in the pleural cavity and its occurrence as a post-operative complication following repair of congenital diaphragmatic hernia is rare. We report here a newborn with this...