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Multiple organ involvement with hydatid cysts
F Sabouni1, F Ferdosian, S Mamishi
1Pediatric Infectious Diseases Research Center and Dept. of Pediatrics, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Insights
Hydatid disease, a rare multi-organ infection, was diagnosed in a 12-year-old boy. Prompt diagnosis and surgical removal of cysts led to successful treatment.
Area of Science:
- Parasitology
- Medical Imaging
- Pediatric Infectious Diseases
Background:
- Hydatid disease (cystic echinococcosis) is a parasitic infection caused by Echinococcus tapeworms.
- While typically affecting the liver and lungs, rare cases involve multiple organs, posing diagnostic challenges.
Observation:
- A 12-year-old boy presented with neurological and constitutional symptoms.
- Imaging revealed extensive cystic lesions in the brain, mesentery, kidney, and heart.
- Serological tests confirmed the presence of hydatid disease.
Findings:
- The patient had concurrent cerebral, cardiac, mesenteric, and renal hydatid cysts.
- Multimodal treatment included antiparasitic drugs (albendazole, praziquantel) and surgical excision of cysts.
- Pathological examination confirmed cystic echinococcosis in all resected lesions.
Implications:
- This case highlights the importance of considering hydatid disease in pediatric patients with multiple unexplained cystic masses.
- Early and accurate diagnosis through imaging and serology is crucial for effective management.
- Multidisciplinary treatment approaches, combining medical and surgical interventions, are essential for favorable outcomes in complex hydatidosis cases.
Abstract:
Hydatid disease is the most common infections worldwide, but it rarely involves multiple organs. Herein, a 12-year-old boy is presented, who was admitted to Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran with symptoms of irritability, sleepless, and weakness of the extremities. Patient's brain computed tomography (CT) scan with contrast media showed large multilocular cystic lesions in right temporal lobe associated with two other smaller similar cystic lesions in centrum semiovale bilaterally. Abdominal sonography revealed intestinal mesenteric and a cardiac cyst. Abdomino-pelvic CT scan showed a cyst medial to the cecum and a cortical cyst in the left kidney as well as a heart cyst. The echocardiography confirmed hydatid cysts at apical and interventricular septum. Serology test was positive for hydatid cyst. Albendazole and praziquantel were started for the patient immediately and right temporal lobe lesions were removed via neurosurgery intervention. After one month, cardiac and mesenteric cysts were operated during two separate surgeries. Pathologic findings of all cysts were compatible with hydatid cyst. Cystic hydatidosis should be suspected in any cystic mass, whilst prompt diagnosis and appropriate treatments are the keys in management of affected patients.
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