Abstract:Background and AimAllergic bronchopulmonary aspergillosis (ABPA) is classified radiologically based on the findings of central bronchiectasis (CB) and other radiologic features (ORF). However, the long-term clinical significance of these classifications remains unknown. We hypothesized that the immunological activity and outcomes of ABPA could be predicted on HRCT chest finding of high-attenuation mucus (HAM), a marker of inflammatory activity. In this study, we evaluate the severity and clinical outcomes of A… Show more
“…Varicose bronchiectasis was considered to be moderate dilatation of the bronchus with irregular bronchial walls showing a beaded appearance. Cystic bronchiectasis was defined as marked saccular dilatation, which appears as a cluster of air-filled cysts [32] ; (2) CB was defined using two different criteria, depending on whether the bronchiectasis was confined to the medial half (point midway between hilum and chest wall) or the medial two-thirds of the lung [33] ; (3) the presence of high attenuation mucus (HAM) was considered if the mucus was visually denser than the paraspinal skeletal muscle [23,34,35] ; (4) centrilobular nodules were considered to be present if the nodules were distributed primarily within the center of the secondary pulmonary lobule with or without a tree-in-bud pattern [36] ; (5) presence of parenchymal abnormalities including consolidation, parenchymal scarring, bullae, atelectasis and pneumothorax were also noted. The criteria used to define these appearances were as described by Webb et al [31] ; and (6) patients were classified radiologically as ABPA-S, ABPA-CB and ABPA-CB-HAM based on the presence or absence of CB and HAM [35] .…”
AIM:To investigate the chest radiographic and high resolution computed tomography (HRCT) chest manifestations in glucocorticoid-naïve allergic bronchopulmonary aspergillosis (ABPA) patients.
METHODS:This is a prospective observational study and includes 60 consecutive glucocorticoid-naïve patients with ABPA who underwent chest radiography and HRCT of the chest (1.25 mm every 10 mm) in the routine diagnostic workup for ABPA.
RESULTS:Chest radiographs were normal in 50% of cases. Of the remainder, most patients demonstrated permanent findings in the form of parallel line and ring shadows suggesting bronchiectasis. Consolidation was detected in 17 cases but in the majority, the corresponding HRCT chest scan showed mucus-filled bronchiectatic cavities. Chest HRCT was normal in 22 patients, while central bronchiectasis (CB) was demonstrated in the remaining 38 patients. Bronchiectasis extended to the periphery in 33%-43% depending on the criteria used for defining CB. The other findings observed on HRCT were mucoid impaction, centrilobular nodules and high-attenuation mucus in decreasing order of frequency.
CONCLUSION:Patients with ABPA can present with normal HRCT chest scans. Central bronchiectasis cannot be considered a characteristic feature of ABPA as peripheral bronchiectasis is commonly observed. Consolidation is an uncommon finding in ABPA.
“…Varicose bronchiectasis was considered to be moderate dilatation of the bronchus with irregular bronchial walls showing a beaded appearance. Cystic bronchiectasis was defined as marked saccular dilatation, which appears as a cluster of air-filled cysts [32] ; (2) CB was defined using two different criteria, depending on whether the bronchiectasis was confined to the medial half (point midway between hilum and chest wall) or the medial two-thirds of the lung [33] ; (3) the presence of high attenuation mucus (HAM) was considered if the mucus was visually denser than the paraspinal skeletal muscle [23,34,35] ; (4) centrilobular nodules were considered to be present if the nodules were distributed primarily within the center of the secondary pulmonary lobule with or without a tree-in-bud pattern [36] ; (5) presence of parenchymal abnormalities including consolidation, parenchymal scarring, bullae, atelectasis and pneumothorax were also noted. The criteria used to define these appearances were as described by Webb et al [31] ; and (6) patients were classified radiologically as ABPA-S, ABPA-CB and ABPA-CB-HAM based on the presence or absence of CB and HAM [35] .…”
AIM:To investigate the chest radiographic and high resolution computed tomography (HRCT) chest manifestations in glucocorticoid-naïve allergic bronchopulmonary aspergillosis (ABPA) patients.
METHODS:This is a prospective observational study and includes 60 consecutive glucocorticoid-naïve patients with ABPA who underwent chest radiography and HRCT of the chest (1.25 mm every 10 mm) in the routine diagnostic workup for ABPA.
RESULTS:Chest radiographs were normal in 50% of cases. Of the remainder, most patients demonstrated permanent findings in the form of parallel line and ring shadows suggesting bronchiectasis. Consolidation was detected in 17 cases but in the majority, the corresponding HRCT chest scan showed mucus-filled bronchiectatic cavities. Chest HRCT was normal in 22 patients, while central bronchiectasis (CB) was demonstrated in the remaining 38 patients. Bronchiectasis extended to the periphery in 33%-43% depending on the criteria used for defining CB. The other findings observed on HRCT were mucoid impaction, centrilobular nodules and high-attenuation mucus in decreasing order of frequency.
CONCLUSION:Patients with ABPA can present with normal HRCT chest scans. Central bronchiectasis cannot be considered a characteristic feature of ABPA as peripheral bronchiectasis is commonly observed. Consolidation is an uncommon finding in ABPA.
“…Only one published trial, stratified or otherwise, distinguished ABPA patients without bronchiectasis (''ABPAserologic'') from those with bronchiectasis [120,150]; those with hyperattenuating mucoid impaction have not been compared with those without impaction, despite apparent differences in severity of immunopathology and prognosis [13,151].…”
Severe asthma with fungal sensitisation and allergic bronchopulmonary aspergillosis encompass two closely related subgroups of patients with severe allergic asthma. Pulmonary disease is due to pronounced host inflammatory responses to noninvasive subclinical endobronchial infection with filamentous fungi, usually Aspergillus fumigatus. These patients usually do not achieve satisfactory disease control with conventional treatment of severe asthma, i.e. high-dose inhaled corticosteroids and long-acting bronchodilators. Although prolonged systemic corticosteroids are effective, they carry a substantial toxicity profile. Supplementary or alternative therapies have primarily focused on use of antifungal agents including oral triazoles and inhaled amphotericin B. Immunomodulation with omalizumab, a humanised anti-IgE monoclonal antibody, or "pulse" monthly high-dose intravenous corticosteroid, has also been employed. This article considers the experience with these approaches, with emphasis on recent clinical trials. @ERSpublications Treatment of fungal asthma includes glucocorticoids, azoles, amphotericin and anti-IgE. Trial validation is needed.
“…[18] Agarwal et al included a new subtype known as ABPA-HAM (highly attenuated mucous). [19] The best thing about ABPA is its response to oral corticosteroids, which further necessitates an earlier diagnosis. Oral corticosteroids suppress both the immune response as well as the inflammation.…”
AbstractsAllergic Bronchopulmonary Aspergillosis (ABPA) is an under diagnosed respiratory condition, which very often masquerades as Bronchial Asthma and results in a delay in identification and subsequent treatment. It is one of the components of the spectrum of aspergillosis -which is a group of diseases caused by the fungi Aspergillus fumigatus. It occurs due to an exaggerated response of the immune system to the fungi. It has a wide variety of presentations, most commonly occurring as fleeting opacities on chest x rays. We present an interesting case of ABPA having a unique presentation.
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