gms | German Medical Science

133. Kongress der Deutschen Gesellschaft für Chirurgie

Deutsche Gesellschaft für Chirurgie

26.04. - 29.04.2016, Berlin

Two surprising intraoperative Meckel diverticulum diagnosis: a Case Review

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  • Duarte Vaz Pimentel - Klinikum Ernst von Bergmann, Klinik für Kinderchirurgie, Potsdam, Deutschland
  • Petra Degenhardt - Klinikum Ernst von Bergmann, Klinik für Kinderchirurgie, Potsdam, Deutschland

Deutsche Gesellschaft für Chirurgie. 133. Kongress der Deutschen Gesellschaft für Chirurgie. Berlin, 26.-29.04.2016. Düsseldorf: German Medical Science GMS Publishing House; 2016. Doc16dgch337

doi: 10.3205/16dgch337, urn:nbn:de:0183-16dgch3374

Published: April 21, 2016

© 2016 Vaz Pimentel et al.
This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License. See license information at http://creativecommons.org/licenses/by/4.0/.


Outline

Text

Background: Meckel diverticulum is the most frequent gastrointestinal malformation affecting 2% of the population. Complications are reported to occur in 2-40% of patients. Despite several modern diagnostic modalities, diagnosis of Meckel diverticulum is still a challenge. The authors report two surprising cases that presented with untypical clinical features and diagnostic results in which the final diagnosis of Meckel diverticulum could only be made intraoperatively. Both patients recovered uneventfully.

Results: The first case refers to a boy that had an intraabdominal cystic formation in the pre-natal ultrasound screening. At 3 years of age he presented in our emergency department after the mother noticed two episodes of dark bloody stool. A technecium-99m scan showed focal activity in the right lower abdominal quadrant, but the area was extremely large so our radiologists considered it to be an untypical Meckel diverticulum image (more likely a vascular malformation or tumor). An MRI showed only a thickened intestinal loop. Intraoperatively the diagnosis of an extremely large Meckel diverticulum with a 6 cm base was made, the intestinal segment was surgically removed and the patient recovered uneventfully. The pathology report described heterotopic gastric mucosal tissue with no malignity.

The second case refers to a 4 year old boy that presented to our emergency department with typical gastroenteritis clinical features. One day later he developed an ileus. An abdominal x-ray showed a foreign body in the pelvis. Intraoperatively a perforated Meckel diverticulum with a button battery at the perforation site was seen. The intestinal segment was surgically removed and the patient recovered without further complications.

Conclusion: Meckel diverticulum still poses a diagnostic challenge for pediatricians and pediatric surgeons. A careful attention to patient history and examination are of the utmost importance, as is a correct diagnostic process. In spite of modern diagnostic tools in some cases the final diagnosis can only be made intraoperatively (sometimes with most surprising findings!).

Figure 1 [Fig. 1]