ISSN: 2161-0517
Case Report - (2012) Volume 1, Issue 3
Fungal infections can colonize in lung cavities mostly in immunocompromised patients. Aspergillosis can develop in cavities formed due to tuberculosis, bronchiectasis, sarcoidosis, lung abscess and cavitary neoplasms. Pulmonary aspergillosis has been reported rarely in pulmonary cavities after the removal of hydatid cyst. We report a case in an immunocompetant patient in whom co-existence of echinococcosis and aspergillosis was detected which is extremely rare. For the better management of the patient while dealing with hydatid cyst, concurrence of aspergillosis should be kept in mind.
<Keywords: Hydatid cyst, Aspergillosis, Immunocompetant
Fungal infections can colonize in lung cavities mostly in immunocompromised patients. Aspergillosis can develop in cavities formed due to tuberculosis, bronchiectasis, sarcoidosis, lung abscess and cavitary neoplasms [1]. Pulmonary aspergillosis has been reported rarely in pulmonary cavities after the removal of hydatid cyst [2-4]. We report a case in an immunocompetant patient in whom co-existence of echinococcosis and aspergillosis was detected which is extremely rare. For the better management of the patient while dealing with hydatid cyst, concurrence of aspergillosis should be kept in mind.
A 42 years old male was presented with irregular fever and hemoptysis for a duration of one month. He had a history of hydatid cyst of left lung for which he was operated one year back. CT(computed tomography) of thorax showed a large heterogeneous mass of 80 × 73 × 45 mm3 with air bronchogram and bronchiologram seen involving posterior-medial basal segment of left lower lobe and posterior segment of left upper lobe with surrounding ground glass opacity, speculation from surface and extension along major fissure with satellite nodule (Figure 1). Radiologically the provisional diagnosis of carcinoma of lung (broncho-alveolar carcinoma) was made.
Routine laboratory examination did not reveal any abnormality except a mild degree of anemia, with a hemoglobin level of 10.6 g/ dl. Total and differential counts were within normal limit. Serum was non-reactive for human immunodeficiency virus. Repeated sputum smears were negative for acid-fast bacilli. The patient underwent surgery, and a wedge resection specimen was sent for histopathological evaluation. Gross received was multiple bits of cystic structures together measuring 20 × 10 × 2 cm3 containing mucinous material. In cut-section, an area of brownish necrotic material was seen (Figure 2). Microscopic examination of the cyst wall revealed the laminated membrane of a hydatid cyst with massive infiltration of fungal hyphae, consistent with aspergillosis (Figure 3). Histochemically, periodic acid- Schiff (PAS) stain was applied and the co-existence of hydatid cyst with Aspergillosis was confirmed. Culture of the tissue grew aspergillus fumigatus. The patient was treated for hydatid disease with albendazole and itraconazole for aspergillosis. The patient was free of any recurrence of either the disease when followed up for another 10 months.
Figure 3: Photomicrography of laminated hydatid cyst wall with infiltration of fungal hyphae (H&E,x100).
Hydatid cyst (echinococcosis) is a parasitic disease which is most commonly caused by Echincoccus granulosus, but Echinococcus multilocularis is the most common type causing pulmonary infection.It most commonly involves two blood filtering organs, the lungs and liver, but can affect any organ of the body [5]. Aspergillosis is a saprophytic fungal infection. Aspergillus fumigatus is the most common cause of aspergillosis in human beings [6]. Aspergillus may cause allergic pulmonary aspergillosis, aspergilloma, and semi-invasive and invasive aspergillosis [6].
Development of aspergillosis in hydatid cyst cavities is rare. Aspergillosis in an operated hydatid cavity was reported after many years in one case and after six months in another case [3,4]. Although immunocompromised patients are more prone to aspergillosis, the co-existence of aspergillosus and hydatid cyst has been reported in both immunocompromised and immunocompetant patients [7,8]. Our patient who was immunocompetant was unique in that in a postoperative cavity again hydatid cyst developed which was secondarily infected with aspergillosus. Aspergillosis was invading the wall of ruptured hydatid cyst as seen in histopathology.
Approximately 60% of pulmonary hydatid disease affects the right lung and 50-60% involves the lower lobes [9] but, our case had developed the lesion in the left lung. The clinical presentation of pulmonary hydatid cysts depends on whether the cyst is intact or ruptured. Intact cysts are either incidental finding or present with cough, dyspnoea or chest pain. A complicated cyst is that which has ruptured into a bronchus, pleural cavity or biliary tree. In ruptured cyst besides these symptoms, the patient may present with expectoration of cystic contents, repetitive hemoptysis, productive sputum, fever, or anaphylactic shock which might be the cause for hemoptysis in our case. Whether the hydatid cyst ruptured spontaneously or because of the invasion of aspergillosis is speculative. Wedge resection was opted for recurrent hemoptysis in our case since the surrounding lung tissue was healthy and this was recommended by others [10].
While dealing with hydatid cyst the co-existence of aspergillosis should always be kept in mind for the better management of the patient.