Co-Existence of An Unusual Branching Pattern of Celiacomesenteric Trunk With Complete Common Mesentery in a 48-Year-Old Man: A Case Report

Author:

Harrabi Fathia1,Jabeur Methnani23ORCID,Houssem Ammar1,Abdelkader Mizouni1,Mehdi Ben Latifa1,Mohamed Amine Saiid1,Mohamed Ben Mabrouk1,Ali Ben Ali1

Affiliation:

1. Department of General Surgery, Sahloul University Hospital, Sousse, Tunisia

2. LR12SP11, Biochemistry Department, Sahloul University Hospital, Sousse, Tunisia

3. LR19ES09, Laboratoire de Physiologie de l’Exercice et Physiopathologie: de l’Intégré au Moléculaire Biologie, Médecine et Santé, Faculty of Medicine of Sousse, Sousse, Tunisia

Abstract

Celiacomesenteric trunk (CMT) refers to the common origin of celiac trunk and superior mesenteric artery which is a very rare anatomical variation. CMT is incidentally diagnosed during angiography or abdominal computed tomography scanning. The diagnosis of CMT may inform surgical practice and prevent damage during invasive radiologic procedures, lowering thus the rate of iatrogenic errors. Complete common mesentery is in its turn a rarer congenital anomaly that arises from an abnormal rotation of primitive small intestine during embryonic development. We report a case of a 48-year-old man, suffering from chronic abdominal pain, and postprandial discomfort. The patient underwent an abdominal contrast-enhanced computed tomography that detected a CMT associated with common complete mesentery. According to our review of bibliography, this is the first case report to simultaneously report both congenital anomalies (CMT and common complete mesentery). Furthermore, the CMT described here has not been described in previous classifications and represent a novel anatomical variation of CMT.

Publisher

SAGE Publications

Subject

Public Health, Environmental and Occupational Health,Health (social science)

Reference16 articles.

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