Pericardial, pulmonary and hepatic hydatid cyst

Autor: B. Abou-Bekr, O. Riffi, S.N. Klouche djedid, AK.mohammed emam hassen, A. ouadah
Jazyk: angličtina
Rok vydání: 2022
Předmět:
Zdroj: Journal of Pediatric Surgery Case Reports, Vol 78, Iss , Pp 102207- (2022)
Druh dokumentu: article
ISSN: 2213-5766
DOI: 10.1016/j.epsc.2022.102207
Popis: 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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