Author/Authors :
Ahmed, Kotti Department of Pediatric Surgery - Hedi Chaker Hospital, 30219 Sfax, Tunisia , Mahdi, Ben Dhaou Department of Pediatric Surgery - Hedi Chaker Hospital, 30219 Sfax, Tunisia , Hayet, Zitouni Department of Pediatric Surgery - Hedi Chaker Hospital, 30219 Sfax, Tunisia , Hamdi, Louati Department of Pediatric Surgery - Hedi Chaker Hospital, 30219 Sfax, Tunisia , Mohamed, Jallouli Department of Pediatric Surgery - Hedi Chaker Hospital, 30219 Sfax, Tunisia , Riadh, Mhiri Department of Pediatric Surgery - Hedi Chaker Hospital, 30219 Sfax, Tunisia
Abstract :
Heteropagus twins are an extremely rare event with an incidence of 1–2 million live births that represents, sometimes, a real challenge for paediatric surgeons. The majority of cases have complete or partial duplication of the pelvis and/or lower extremities. Thoracic heteropagus conjoined twins is a rare condition in which a grossly defective foetus (the parasite) is attached to the thorax of the main foetus (the autosite). We describe a case of a parasitic heteropagus attached at the chest wall with a rare presentation of giant exomphalos on the autosite. In this situation, the separation procedure was simple after a well-done anatomic study using X-ray, ultrasonography, magnetic resonance and echocardiogram are performed.
Keywords :
Asymmetric conjoined twins , heteropagus twins , incomplete conjoined twins , omphalocele , omphalopagus parasite , parasitic twins