INTRODUCTION: Duodenal duplication is a rare congenital malformation. Although more frequent in childhood, it may rarely be observed in adulthood. Pre-operative diagnosis can be difficult. PRESENTATION OF CASE: We report the case of a 52-year-old man with a duodenal duplication cyst, who was misdiagnosed even after a primary surgery. Definitive treatment needed an extensive diagnostic workup and a second delicate operation. DISCUSSION: This article discusses the incidence of duodenal duplications, their types, their clinical presentations, the radiologic and diagnostic features along with different therapeutic options. CONCLUSION: Duodenal duplication should always be one of the differential diagnoses proposed when approaching upper abdominal cystic formations.
INTRODUCTION: Duodenal duplication is a rare congenital malformation. Although more frequent in childhood, it may rarely be observed in adulthood. Pre-operative diagnosis can be difficult. PRESENTATION OF CASE: We report the case of a 52-year-old man with a duodenal duplication cyst, who was misdiagnosed even after a primary surgery. Definitive treatment needed an extensive diagnostic workup and a second delicate operation. DISCUSSION: This article discusses the incidence of duodenal duplications, their types, their clinical presentations, the radiologic and diagnostic features along with different therapeutic options. CONCLUSION: Duodenal duplication should always be one of the differential diagnoses proposed when approaching upper abdominal cystic formations.
Authors: T Merrot; R Anastasescu; T Pankevych; S Tercier; S Garcia; P Alessandrini; J-M Guys Journal: Eur J Pediatr Surg Date: 2006-02 Impact factor: 2.191