1995
DOI: 10.1136/thx.50.7.809
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Treatment of pulmonary aspergilloma in cystic fibrosis by percutaneous instillation of amphotericin B via indwelling catheter.

Abstract: Pulmonary aspergilloma is a rare complication of cystic fibrosis and is a contraindication to transplantation. The elimination of an aspergilloma in a 24 year old patient with cystic fibrosis by percutaneous instillation of amphotericin B is described, enabling her to be accepted on a lung transplantation programme. (Thorax 1995;50:809-810) Keywords: cystic fibrosis, aspergilloma, Aspergillus, amphotericin B.Poor pulmonary function led to referral for lung transplantation but she was thought unsuitable beca… Show more

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Cited by 12 publications
(10 citation statements)
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“…However, the failure of intracavitary injections of amphotericin B may be explained by insufficient intracavitary levels of the drug or by an insufficient duration of therapy. In the case report by Ryan et al [9], the successful eradication of an aspergilloma was achieved by administration of 3 g of liposomal amphotericin B over the course of 60 days, whereas only 50 mg was administered to our patient. However, our patient had mildto-moderate hemoptysis after instillation, which caused reluctance about giving further intracavitary injections.…”
mentioning
confidence: 82%
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“…However, the failure of intracavitary injections of amphotericin B may be explained by insufficient intracavitary levels of the drug or by an insufficient duration of therapy. In the case report by Ryan et al [9], the successful eradication of an aspergilloma was achieved by administration of 3 g of liposomal amphotericin B over the course of 60 days, whereas only 50 mg was administered to our patient. However, our patient had mildto-moderate hemoptysis after instillation, which caused reluctance about giving further intracavitary injections.…”
mentioning
confidence: 82%
“…Five cases of pulmonary aspergilloma in adults and 5 cases in pediatric/adolescent patients with cystic fibrosis have been reported [1][2][3][4]9]. The majority of patients had long-term morbidity or mortality.…”
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confidence: 94%
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“…The prevalence of aspergillomas in post-tuberculous cavities in the UK may be as high as 10% [12]. Other common causes of the pre-formed cystic host cavity of the aspergilloma include end-stage sarcoidosis [13] or other interstitial lung disease such as pneumoconiosis, bronchiectasis [14] as in cystic fibrosis [15] and/or ABPA, lung abscess, cavitating lung neoplasm [16], pulmonary infarct [17], atypical mycobacterial infection [18], bullous emphysema, hematoma, Pneumocystis jirovecii (formerly P.carinii ) pneumonia (PCP) [19,20], lung surgery [21 Á/23] ankylosing spondylitis, and the cavitary residue of invasive fungal infection [24,25]. Unusually, aspergillomas have been described in immunocompetent patients who do not appear to have had a pre-existing dilated lung space [26,27].…”
Section: Clinical Backgroundmentioning
confidence: 99%