Methods: Between January 2000 and January 2018, a total of 45 consecutive patients (27 males, 18 females; mean age 46.4±13.5 years; range, 23 to 78 years) who underwent fiberoptic bronchoscopy to establish the definitive diagnosis following radio-diagnostic procedures were retrospectively analyzed. Data including demographic and clinical characteristics of the patients, preoperative diagnostic studies, bronchoscopic findings, and postoperative diagnosis were recorded.
Results: Endobronchial hyperemia (n=42) and purulent secretion (n=34) are the most common findings of bronchoscopy. The most specific finding was the presence of pieces of cystic membranes in 23 patients. Scolices were seen in five patients in bronchial aspirate. In one patient, both pieces of cystic membranes and scolices in bronchial aspirate were detected. The preliminary diagnosis of a hydatid cyst was made based on these findings in 28 patients (62.2%) preoperatively. The definitive diagnosis of a hydatid cyst was confirmed through thoracotomy in all patients.
Conclusion: Bronchoscopy is a particularly valuable method in the definitive diagnosis of ruptured lung hydatid cysts. The definite diagnosis is based on the visualization of the endobronchial membrane during bronchoscopy or scolices in the bronchial aspirate. It can be also used to prevent complications such as bronchial dissemination and asphyxia due to intra-bronchial membrane pieces.
Fiberoptic bronchoscopy has been increasinly used in pulmonary diseases and is effective in the diagnosis of various pathologies. However, there is a very limited number of studies in the literature regarding the diagnosis of hydatid disease using fiberoptic bronchoscopy.
In the present study, we aimed to evaluate the diagnostic yield of fiberoptic bronchoscopy in ruptured pulmonary hydatid cysts which are indistinguishable from pulmonary masses on imaging techniques.
Thoracic X-ray and computed tomography (CT) were performed in all patients. Bronchoscopy was performed in all patients either due to negative radiographies for hydatid cysts or to eliminate malignancy. Bronchoscopies were performed using a flexible fiberoptic bronchoscope. Two types of fiberoptic bronchoscope (Olympus BF 20D and BF 1T240, models of Olympus Optical Co. Ltd., Tokyo, Japan) were used for the bronchoscopic examination. The patients were sedated with 5 mg diazepam and, during the procedure, local anesthesia was administered to all patients with the instillation of 2% prilocaine hydrochloride solution. The transnasal route was used during bronchoscopy. Bronchial lavage specimens were taken for smear and culture testing. The diagnosis of pulmonary hydatid disease was based on the direct visualization of hydatid membrane or microscopically confirmation of scolices. Nine patients in whom a diagnosis was not made either from radiological techniques, or laboratory or bronchoscopy underwent thoracotomy to rule out malignancy. Data including demographic and clinical characteristics of the patients, preoperative diagnostic studies, bronchoscopic findings, and postoperative diagnosis were recorded.
Statistical analysis
The IBM SPSS version 20.0 software (IBM Corp.,
Armonk, NY, USA) was used for statistical analyses.
Data are presented as mean, standard deviation,
median; and with the minimum and maximum values,
numbers and percentages. A p v alue < 0.05 w ere
considered as statistically significant.
Figure 1. An axial computed tomography image showing a ruptured right lung hydatid cyst.
Figure 2. An axial computed tomography image showing a ruptured right lung hydatid cyst.
Figure 3. A bronchoscopic image showing germinal membrane in ruptured hydatid cyst.
The mean time between the initial symptom to bronchoscopy was 21.6 (range, 6 to 54) days. Endobronchial hyperemia was found in 42 (93.3%) of the patients. The definitive diagnosis was made by detecting germinative membranes in 23 patients (51.1%) and by the presence of scolices in the bronchial aspirate in five patients (11.1%) (Figures 4a-c). The preliminary diagnosis of a hydatid cyst was made based on these findings in 28 patients (62.2%) preoperatively. All patients were, then, treated surgically with posterolateral thoracotomy. The applied operation types included cystotomy and capitonnage (n=37, 84.4%) and cystectomy and capitonnage (15.6%, n=8). There were no postoperative complications or mortality after bronchoscopy or surgery. Albendazole was administered to all patients after the operation for one to three months. The mean follow-up was 4.5 years (range, 3 months to 7 years). Demographic and clinical data and procedure-related data are summarized in Table 1.
Table 1. Demographic and clinical characteristics of patients and procedure-related data
In areas where hydatid cysts is endemic, thoracic CT is usually sufficient for the diagnosis of intact simple hydatid cysts. It also provides important data in differential diagnosis. When the hydatid fluid is emptied completely from the pericystic cavity, the residual membrane constitutes more homogeneous opaque appearance and the size of the lesion becomes smaller.[9,10] T he C T d ensity v alues r ange f rom 42 to 60 HU in simple hydatid cysts, while it ranges from 9 to 160.5 HU in ruptured hydatid cysts.[11] The higher attenuation values represent the fibrosis and infection of the cyst. The increased densities due to residual membrane after the drainage of the cystic fluid and the beginning of the infectious process can be misdiagnosed with other lung diseases particularly with malignant carcinomas. Bronchoscopy is particularly the choice of the diagnostic methods, when a centrally located, ruptured cyst hydatid simulates the radiological findings of malignant mass lesions. To rule out malignancy, this method was considered more time-saving and cost-effective, compared to other diagnostic methods.
The bronchoscopy procedures which are made for the differential diagnosis can provide diagnostic findings specific to the cyst. Saygi et al.[12] provided bronchoscopic diagnosis in 14 of 24 patients (58%) in whom complicated pulmonary hydatid disease diagnosis was confirmed by thoracotomy. In our study, we made the definitive diagnosis in 23 patients based on the presence of endobronchial membranes on bronchoscopy which was performed for the differential diagnosis of the mass or cavitary lesion. The detection of scolices on histological examination of the bronchial lavage, despite the absence of membranes provided definitive preoperative diagnosis in five patients. In our opinion, low accuracy of cytological diagnosis is mainly due to total expectoration of the hydatid fluid. In addition, we believe that, in our study group, the mean delay of bronchoscopic evaluation led to difficulty in cytological diagnosis of hydatid materials. The accuracy of preoperative diagnosis of bronchoscopy was 62.2% as confirmed by postoperative results.
Furthermore, bronchial spreading of the hydatid fluid and the obstruction due to membranes may be fatal. In addition to lavage and aspiration during bronchoscopy, the extraction of the pieces of the membrane becomes preventive for possible complications. The extraction of membrane pieces only by bronchoscopy is not a safe procedure for the treatment. Pericystic cavity and residual membranes continue to become a source to recurrent infection, even if some parts of the membrane are being extracted. Surgical approach is necessary for the treatment of the residual pericystic cavity, despite this procedure.[10]
The main limitations of the present study include its small sample size and retrospective design.
In conclusion, the confirmation of the diagnosis by fiberoptic bronchoscopy in uncertain cases is both a simple and cost-saving approach. The definitive diagnosis can be made during this procedure in selected patients. Tracheobronchial complications of ruptured hydatid cysts can be also controlled during bronchoscopy, thereby, preventing complications such as bronchial dissemination and asphyxia due to intra-bronchial membrane pieces.
Declaration of conflicting interests<7b>
The authors declared no conflicts of interest with respect to
the authorship and/or publication of this article.
Funding
The authors received no financial support for the research
and/or authorship of this article.
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