
Granulomatous Appendicitis- A Rare Case Report
ED01-ED03
Correspondence
Dr Usha Muniyappa,
Assistant Professor, Department of Pathology, MS Ramaiah Medical College, Bengaluru-560054, Karnataka, India.
E-mail: usharavihitha@gmail.com
In 1953, Meyerding and Bertram were the first individuals to report non-specific granulomatous inflammation in the appendix. Granulomatous appendicitis is a rare condition, accounting for less than 2% of cases. However, idiopathic granulomatous appendicitis is very rare, and diagnosis is usually made by excluding all other conditions. It is challenging to diagnose tuberculous appendicitis based on clinical findings, hence histopathological examination is required. Hereby, authors report a case of 26-year-old male who presented with pain abdomen in the Department of Surgery. On imaging, appendix was thickened, and acute appendicitis was considered as a probable diagnosis. On histopathological examination, it was diagnosed as granulomatous inflammation suggestive of tuberculosis. The present case is presented for its rarity as appendicitis is considered as an abdominal emergency, so prompt management and diagnosis is required by excluding all other causes of granulomatous inflammation in appendix.