Cystic echinococcosis or hydatid disease affects 1 million people every year worldwide (1). Cystic lesions associated with hydatid disease are caused by the larvae of the tapeworm
A 68-year-old man presented to pulmonology outpatient department in March 2018 with a 2-month history of productive cough with sputum production (initially 100 mL/day of grey sputum and sometimes with solid white pieces, which had gradually become purulent). He was treated with amoxicillin orally for 10 days, but due to worsening conditions (severe left chest pain, fever 39°C and breathlessness) he was hospitalised. The patient has never smoked, but he reported biomass fuel exposure. His medical history was significant for liver cirrhosis, atrial fibrillation, arterial hypertension and New York Heart Association (NYHA) third-class heart failure. No chest radiographs were performed in the previous 10 years. Also, he had reported a prolonged exposure to dog and sheep. On chest radiography, the displacement of the trachea to the right, an apparent elevation of the left hemidiaphragm, bibasilar opacities and ill-defined cavities suggestive for the formation of lung abscess or cystic bronchiectasis were seen (Figure 1). Treatment with ceftriaxone and metronidazole was started. Mild eosinophilia (819 cells/μL), thrombocytopaenia (platelet count 120 × 103/μL, attributed to hypersplenism) and moderate increase in erythrocyte sedimentation rate (36 mm/h) were identified. Low total protein level and hypoalbuminaemia secondary to his cirrhosis were also found. On the 6-th day of admission, a thoracic high-resolution computer tomography (HRCT) was performed (Figure 2). This revealed three well-defined cavitary lesions with different contents. In the left upper lobe, a well-circumscribed lesion (Figure 2A and B) around 4 cm in diameter, with smooth walls, predominantly of fluid attenuation content (12 HU) was identified. In the left lower lobe anteromedial segment, the lesion was 5 cm in diameter with thickened irregular walls (Figure 2D–F), dense content and the air crescent signs (moon sign and meniscus sign). In the right lower lobe posterolateral segment, another 5-cm thin-walled cavity with lobulated air–soft tissue interface (‘air bubble’ sign suggestive for ruptured and infected HC) was found (Figure 2G and H). No liver involvement was documented. Serum
Posteroanterior view of chest X-ray showing bibasilar opacities and ill-defined cavities (arrows) suggestive for forming lung abscess or cystic bronchiectasis. Note the elevation of the left hemidiaphragm with mediastinal shift and displacement of the trachea to the right.
The high-resolution computer tomography images demonstrate three well-defined cavitary lesion with different inside contents.
Colony of
A fiberoptic bronchoscopy was performed and it did not reveal any abnormality. Culture and microscopy of bronchoalveolar lavage (BAL) were also negative for gram-negative and gram-positive bacteria as well as for
The multiple round cysts and positive
Due to multiple lung cysts and associated co-morbidities, surgery was not considered and albendazole plus itraconazole in standard doses were started. The treatment was interrupted after 1 month due to side effects (nausea, vomiting and loss of appetite). The patient continued to complain of dry cough and moderate dyspnoea.
Three months later, a follow-up CT showed the upper left lobe cyst (Figure 4A and B) unchanged in size, borders and density (2–3 HU). A reduction in size of the right (Figure 4C and D) and left (Figure 4E and F) lower lobes cysts with an increased density of the content (30–60 HU) was observed.
A follow-up CT (3 months later) shows the upper left lobe cyst (
In August 2018, after 6 months since the initial hospitalisation, the patient was admitted again for a new episode of severe dyspnoea, left side chest pain, cough and high fever. Chest radiography showed new areas of consolidation in the lower lung fields (Figure 5A). A communicating rupture of the upper left lobe cyst or bacterial superinfection was suspected. Antibiotic treatment with ceftriaxon and ciprofloxacin was initiated. Five days later, chest radiography showed partial resolution of pulmonary infiltrates on the left side (Figure 5B).
After hospital discharge, the patient remained with no antibiotic, antifungal or antiparasitic medication till March 2019, when another exacerbation episode occurred. This time, the patient complained of severe cough and copious sputum production (Figure 6C), wheezing, fever and chest pain. On admission, chest radiography (Figure 6A and B) identified previous cavitary lesions increased in size and signs of ruptured cyst in the left upper lobe. Contrast-enhanced computed tomography (Figure 7) confirmed the intrabronchial rupture of left upper lobe cyst (‘onion peel sign’ or ‘Cumbo’ sign), and the increase in size of the left and right lower lobes cysts (suggestive for secondary infection). Since then, the patient has not experienced other exacerbations.
Contrast-enhanced computed tomography shows hydatid cyst in left upper lobe (
Hydatid disease continues to be a challenging medical problem and it should be considered in the differential diagnosis of cystic pulmonary lesions (3). It commonly occurs in persons with a prolonged exposure to the intermediate hosts of
Symptoms associated with a complicated pulmonary hydatid disease include sudden onset of chest pain, cough, fever and haemoptysis. Perforation of the cysts into a bronchiole could result in hydatoptysis – expectoration of the germinative membrane or the hooklets of the parasite (4). Cough could be productive of purulent sputum in case of infection.
Pulmonary lesions have three components, and they are important for understanding the radiographic appearance of pulmonary HCs. The outermost part is called the pericyst and it consists of compressed lung tissue and fibrosis adjacent to the parasite. The parasite itself is composed of two layers, namely an outer layer or ectocyst and an inner layer or endocyst, from which daughter cysts bud.
Radiological features of pulmonary hydatid disease vary from pure cystic lesions to a completely solid mass, which implies a large list of differential diagnosis that includes tuberculosis, primary and secondary tumours, lung abscess, bacterial bronchopulmonary infections, polyangiitis with granulomatosis, bronchiectasis, pneumothorax, pleurisy and empyema (10). Daughter cyst formation and calcification of the cyst walls are common in the liver but rare in the lung (~1% of cases) (4,10).
Although typical imaging findings have been well described in the literature, atypical imaging presentation can occur secondary to cyst rupture. Some authors suggested to differentiate the radiological features of ruptured HCs into contained cyst rupture signs (rupture of the pericyst which leads to dissection of air between the pericyst and ectocyst – ‘air crescent’ or ‘meniscus’ sign) and complete cyst rupture signs (rupture of the exocyst, with the expulsion of some fluid contents, allowing the endocyst to collapse – ‘Cumbo’, ‘onion’, ‘whirl’, ‘water-lily’, ‘mass within a cavity’, ‘dry cyst’ signs) (11,12).
In case of infected HCs, radiography can show a thick-walled structure, similar to lung abscesses, with air-fluid level and a pneumonic consolidation area surrounding it. On CT, an increase in density of cystic lesions (>20 HU) is suggestive for superimposed infection, making difficult the differentiation with abscess or tumour. ‘Air bubble’ sign could be helpful in this regard. The ‘air bubble’ sign is better seen in the mediastinal window and consists of single or multiple small rounded radiolucent areas with sharp margins within the periphery of a solid mass lesion (4,13,14). It is caused by air entering into the cyst by erosion of the bronchiolar wall or gas production by secondary bacterial infection.
Routine haematological and biochemical tests show unspecific results in echinococcosis. Blood eosinophilia might occur in minority of patients when a leakage of antigen materials occurs (3,15). In clinical practice, detection of specific serum IgG antibodies supports the diagnosis with a specificity ranging between 50% and 90%. False-positive IgG results could be caused by other parasitic diseases. False-negative results are more common in pulmonary than in hepatic echinococcosis and they are associated with an intact, calcified or non-viable cyst (16). Complication with secondary infections requires specific additional laboratory workup.
Bacterial pneumonia is the most frequently reported secondary infection associated with pulmonary HCs. Commonly isolated bacterial germs belong to streptococci group (5,6). In liver hydatids, infection with
Surgery, even in cases with bilateral involvement, is the treatment of choice in HC patients who can undergo intervention. Therapy with benzimidazoles (mebendazole or albendazole) is valuable in disseminated disease, high surgical risk patients and pre- and post-surgical prophylaxis. Evaluation of treatment success is difficult and it usually implies regular clinical and imaging follow-up. Assessment of serological titres could be helpful for therapy response monitoring (3).
Despite the apparently typical clinical presentation of lung echinococcosis, our case clearly illustrates the role of a detailed imaging assessment for a proper diagnosis and clinical decision-making. The variety of concomitant imaging appearances (intact cyst, ‘air bubble’, ‘crescent’, ‘onion peel’ signs) detected during the initial hospitalisation was crucial for further laboratory assessment and prompt diagnosis of a rare coexistence of echinococcosis and aspergillosis.
This case also illustrates clinical challenges in patients with HC who are not eligible for surgical treatment. One of the most significant points in this regard is the importance of regular imaging and microbiological follow-up, particularly important during exacerbation of each symptom. Thus, detailed follow-up imaging during exacerbation of symptoms in our patients was helpful for proving rupture of HCs and secondary bacterial coinfection. The evolution of radiological signs was useful for making decisions about the regression of fungal–bacterial coinfection on antibiotic treatment during the exacerbations.
In our patient, it was not possible to ensure a sustainable administration of antiparasitic and antimycotic medication due to side effects. However, antibiotic and antifungal medication for 1 month improved symptoms and diminished both lower lobe cysts size on follow-up CT 3 months later (Figure 4C–F). Currently, there is no generally accepted duration of antifungal treatment in cases of coexisting aspergilloma and pulmonary HC with no surgical treatment (19). This is partially due to the fact that majority of reported cases are diagnosed retrospectively after surgical removal of the cyst (7,8,17,20). Further reporting of similar coinfected, surgically untreatable cases will contribute to a better management of these patients.
We have presented a case with multiple pulmonary echinococcal cysts, complicated by rupture and superimposed infections, which was treated medically. This is one of the few reports of a response to medical treatment alone in an adult patient with concurrent infections and multiple co-morbidities.