Hydatid disease is responsible for causing cystic disease. In children, it classically involves the liver, lung and brain but can involve almost any organ or numerous organs simultaneously. The lung is the most common target organ in children, while in adults hepatic involvement is more common. We present three case reports of children who presented with hydatid disease with varying clinical manifestations of pulmonary hydatidosis and complications, and their related management.
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Case presentations
Case 1The first case is an 11-year-old boy referred to our hospital for the assessment of ring lesions seen on X-ray. He was from a rural area of KwaZulu-Natal Province. He had a 3-month history of cough, fever and loss of appetite. He had no history of tuberculosis (TB) contact. On examination he was wasted, had tachypnoea and had bilateral crackles in both lung fields. The rest of the system examination was normal. His chest X-rays showed bilateral well-circumscribed round lesions (Fig. 1). The enzyme-linked immunosorbent assay (ELISA) HIV test was negative and sputum microscopy sensitivity and culture revealed no pathogens. The hydatid indirect haemagglutinin assay was positive and the full blood count smear showed eosinophilia. A diagnosis of bilateral diffuse echinococcosis was made. The thoracic surgeons were consulted; however, because of the extent of the disease, with multiple lesions bilaterally, the agreed therapeutic option was a trial of medical treatment, as the lesions were inoperable. Medical management was then instituted with albendazole 400 mg/day for 6 months. The follow-up X-rays showed dramatic improvement of the lesions and good resolution.
Case 2A 5-year-old boy was referred from rural Eastern Cape Province for assessment of a suspected non-resolving pleural effusion. The parents gave a history of progressively worsening symptoms of a tight chest and breathlessness on exertion over the past 3 years. He had been diagnosed with asthma by numerous general practitioners but the symptoms had not improved on treatment. On clinical examination, he had respiratory distress with tachypnoea, bilateral wheezes over both lung fields and decreased air entry. The remaining systems were normal. The chest X-ray revealed an almost complete white-out of the right hemithorax with an air-fluid level (Fig. 2). He had been suspected of having a pleural effusion/empyema at the referral hospital and this had been drained, with clear blood-tinged fluid aspirated. The full blood count smear showed eosinophilia. The hydatid indirect haemagglutination assay was highly positive. Computed tomography (CT) scan confirmed the presence of a large cystic lesion with a thick wall and air-fluid levels (Fig. 3). Ultrasound did not show any lesions in the liver. The child was referred to cardiothoracic surgeons, the lesion operated and a cyst removed (Fig. 4).