Abstract：
BACKGROUND:Meckel's diverticulum (MD) is a congenital anomaly of the small intestine. It results from incomplete obliteration and resorption of the proximal omphaloenteric duct connecting yolk sac with primitive gut in the fetal period. CASE REPORT:A case of 20-year old female with ectopic pancreatic rests in a MD was reported. She was hospitalized with clinical signs of acute appendicitis. During surgery an inflamated Meckel's diverticulum was found and a clinoid resection of the diverticulum was performed. Histologic examination revealed pancreatic tissue in the removed diverticulum. Endocrine cells (EC) were detected with Masson staining and aberrant pancreatic tissue with immunocytochemical LSAB2 method using pan cytokeratin as epithelial marker. CONCLUSION:Most of MD are asymptomatic and accessory finding during laparothomias for different causes, but complications of undiagnozed MD can be serious (diverticulitis, perforation with peritonitis or intestinal obstruction caused by invagination). In unclear cases, additional cytochemical and immunocytochemical diagnostics could be done.
journal_name
Vojnosanit Pregljournal_title
Vojnosanitetski pregledauthors
Pavlović S,Janjić D,Mihajlović S,Stefanović N,Pavlović M,Stanojević G,Stojanović Vdoi
10.2298/vsp1012021psubject
Has Abstractpub_date
2010-12-01 00:00:00pages
1021-4issue
12eissn
0042-8450issn
2406-0720journal_volume
67pub_type
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doi：
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