A rare presentation of perforated Meckel diverticulitis in adulthood.

Abstract

Meckel diverticulum is the most common congenital anomaly of the gastrointestinal tract, often asymptomatic but capable of causing complications such as obstruction, bleeding, or diverticulitis. We present a 54-year-old male who presented with acute lower abdominal pain, leukocytosis, and imaging findings suggestive of Meckel diverticulitis. Surgery revealed signs of perforation, with final pathology confirming the diagnosis. The patient recovered well, with complete symptom resolution by postoperative day 14. This case emphasizes the importance of recognizing complicated Meckel diverticulitis as a surgical emergency and highlights the benefits of minimally invasive, robotic-assisted surgery in optimizing patient outcomes.