Journal of Pediatric Surgery Case Reports (Mar 2022)

Pericardial, pulmonary and hepatic hydatid cyst

  • B. Abou-Bekr,
  • O. Riffi,
  • S.N. Klouche djedid,
  • AK.mohammed emam hassen,
  • A. ouadah

Journal volume & issue
Vol. 78
p. 102207

Abstract

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Pericardial hydatid cyst without cardiac involvement is extremely rare even in endemic countries [1], it results from the development of the larval form of Echinococcus granulosus tapeworm. Only 2–10% of cardiac echinococcosis are characterized by a pericardial cyst formation [2]. Clinical presentation usually regroups dyspnea, weakness, unexplained weight loss. When the localization of the cyst is cardiac, the occurrence of tamponade with fatal outcomes may occur if not treated early [3]. Diagnosis is based on imaging data and assisted by serology. The treatment often combines surgical procedures with medical therapy with albendazole [4]. The pericardial location makes the surgical treatment more challenging. . We report the clinical observation of a 5 years old operated child. We present the case of a 5 year-old boy whose parents sought medical attention due to dyspnea and abdominal mass.

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