International Journal of Health & Allied Sciences

CASE REPORT
Year
: 2016  |  Volume : 5  |  Issue : 2  |  Page : 115--117

Cecal duplication cyst: A rare case report with review of literature


Vikas Shyam Raj Singh, Prasmit Amit Shah, Prakash M Roplekar, S Sudhamani, Prathmesh Desai 
 Department of Pathology, DY Patil University School of Medicine, Navi Mumbai, Maharashtra, India

Correspondence Address:
Vikas Shyam Raj Singh
Department of Pathology, DY Patil University School of Medicine, Nerul, Navi Mumbai - 400 706, Maharashtra
India

Duplication cysts of the alimentary tract are very rare congenital anomalies. Out of all these cases, two-thirds of them manifest before the age of 2 years. They are common in ileum, but very rare in cecum. Some of them may remain asymptomatic and present in the adulthood. The lesion may be tubular or cystic. Several theories have been postulated, but true etiology is not known. We hereby report a case of a 10-year-old female who presented with abdominal pain in the pediatric surgery outpatient department. Diagnosis of cecal duplication cyst was confirmed on histopathology. This report implies that although alimentary tract duplications are rare, they should be considered in the differential diagnosis of children who presents with acute abdominal pain.


How to cite this article:
Singh VS, Shah PA, Roplekar PM, Sudhamani S, Desai P. Cecal duplication cyst: A rare case report with review of literature.Int J Health Allied Sci 2016;5:115-117


How to cite this URL:
Singh VS, Shah PA, Roplekar PM, Sudhamani S, Desai P. Cecal duplication cyst: A rare case report with review of literature. Int J Health Allied Sci [serial online] 2016 [cited 2024 Mar 29 ];5:115-117
Available from: https://www.ijhas.in/article.asp?issn=2278-344X;year=2016;volume=5;issue=2;spage=115;epage=117;aulast=Singh;type=0