S. Thomas et al., HYDATIDEMESIS - A BIZARRE PRESENTATION OF ABDOMINAL HYDATIDOSIS, Australian and New Zealand journal of surgery, 63(6), 1993, pp. 496-498
A 31 year old male presented with high grade fever and abdominal pain
of 20 days duration. At the age of 9 he had been operated on for a sol
itary retroperitoneal hydatid cyst and had been asymptomatic until the
age of 21 when he sustained a blunt injury to the abdomen. An explora
tory laparotomy for splenic rupture revealed multiple intra-abdominal
hydatid cysts, which were removed. The patient remained well until the
present episode. An ultrasound examination revealed multiple intra-ab
dominal hydatid cysts. Seven days after admission, the patient develop
ed hydatidemesis (hydatid cysts and membranes in the vomitus) and hyda
tidenteria (passage of hydatid membranes in the stools), and his pain
and fever subsided. A Gastrografin study and a computerized tomography
(CT) scan revealed hydatid cysts communicating with the stomach and d
uodenum. In view of his disseminated recurrent abdominal hydatidosis,
he was treated with high dose, long-term albendazole along with regula
r follow up. This is the first documented case of disseminated abdomin
al hydatidosis presenting with a cystogastric fistula and hydatidemesi
s.