Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Subacute invasive pulmonary aspergillosis
- Radiologic Findings
- Figure 1. Multiple small nodules are noted in both lungs with cavitary consolidation in right apex.
Figure 2-3. An approximately 4.5cm-sized thick walled cavity with adjacent fibrotic bands is seen in right upper lobe with randomly distributed multiple small nodules in both upper lobes.
Figure 4. On chest X-ray after 1 year, there is increasing cavitary consolidation in RULZ while other findings remain constant.
Figure 5-8. Chest CT scans after 1 year show substantially thickened wall of the cavity with unchanged multiple nodules in both upper lobes.
The patient had a history of tuberculosis and pneumoconiosis. Aspergillus fumigatus was detected in culture by PCNA, and a definitive diagnosis of subacute invasive pulmonary aspergillosis was made.
Figure 9. Increasing wall thickness of cavity is noted on serial CT images: overall size and wall thickness continues to increase until the final month.
- Brief Review
- Subacute invasive pulmonary aspergillosis (SIPA) is a rapidly progressive fungal infection lasting fewer than three months and arising from pre‐existing lung lesions, generally affects moderately immunocompromised patients. Previously known as chronic necrotizing aspergillosis or semi-invasive aspergillosis, it is a subacute to chronic, localized, and indolent form of invasive aspergillosis.
Development of chronic cavitary pulmonary aspergillosis (CCPA) occurs over several months, with the condition commonly relapsing, even after surgery. Over time, if untreated, these cavities enlarge and coalesce, and fungal balls may appear or disappear. The development from CCPA to SIPA is caused by cavity expansion and is found among patients with impaired immunity. SIPA is the progressive enlargement of a single (preexisting) cavity, usually with a thin wall, either progressing slowly over months or rapidly in weeks. The rapidity of installation seems closer to that of invasive forms of aspergillosis in the non-immunocompromised context.
Oral itraconazole is the initial drug of choice and considerably superior to standard supportive therapy, with a relatively safe profile even if administered over several months. Voriconazole is a second-line oral therapy that can be used when adverse effects or failure of therapy occur with itraconazole. Although duration of therapy is variable, a minimum of 6 months is generally recommended. A recently published paper suggested extended antifungal treatment therapy for 12 months for demonstrable clinical improvement. Asymptomatic patients can also be safely observed without antifungal therapy and reassessed every 3–6 months.
- Please refer to
Case 103, Case 508, Case 578, Case 1159, -
- References
- 1. Barac A, Kosmidis C, Alastruey-Izquierdo A, et al. Chronic pulmonary aspergillosis update: A year in review. Med Mycol. 2019 Apr 1;57(Supplement_2):S104-S109
2. Kanj A, Abdallah N, Soubani AO. The spectrum of pulmonary aspergillosis. Respir Med. 2018 Aug;141:121-131
3. Denning DW, Cadranel J, Beigelman-Aubry C, et al. Chronic pulmonary aspergillosis: rationale and clinical guidelines for diagnosis and management. Eur Respir J. 2016 Jan;47(1):45-68.
- Keywords
- lung, chronic pulmonary aspergillosis, subacute invasive pulmonary aspergillosis,