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DOI 10.1016/j.jaip.2019.02.041

Медицинская библиотека · The journal of allergy and clinical immunology. In practice · 2019

Spectrum of Pulmonary Aspergillosis in Hyper-IgE Syndrome with Autosomal-Dominant STAT3 Deficiency.

Duréault Amélie, Tcherakian Colas, Poiree Sylvain, Catherinot Emilie, Danion François, Jouvion Grégory, Bougnoux Marie Elisabeth, Mahlaoui Nizar, Givel Claire, Castelle Martin, Picard Capucine, Chansdesris Marie Olivia, Lortholary Olivier, Lanternier Fanny, French Mycoses Study Group

СтатьяПеревод пока не подготовлен

Аннотация

BACKGROUND

Autosomal-dominant signal transducer and activator of transcription 3 (STAT3) deficiency predisposes to recurrent bacterial pneumonia, complicated by bronchiectasis and cavitations. Aspergillosis is a major cause of morbidity in these patients. However, its diagnosis, classification, and treatment are challenging.

OBJECTIVE

We aimed to assess the prevalence and describe the clinical, mycological, and radiological presentation and related therapy and outcome of Aspergillus infections of the respiratory tract in the STAT3-deficient patients of the National French cohort.

METHODS

We performed a retrospective study of all pulmonary aspergillosis cases in STAT3-deficient patients (n = 74). Clinical and mycological data were collected up to October 2015 and imaging was centralized.

RESULTS

Twenty-one episodes of pulmonary aspergillosis in 13 (17.5%) STAT3-deficient patients were identified. The median age at first episode was 13 years (interquartile range, 10-26 years). Ninety percent of patients had previous bronchiectasis or cavitations. Infections were classified as follows: 5 single aspergilloma, 9 chronic cavity pulmonary aspergillosis, 5 allergic bronchopulmonary aspergillosis-like disease, and 2 mixed forms of concomitant allergic bronchopulmonary aspergillosis-like disease and chronic cavity pulmonary aspergillosis. No invasive aspergillosis cases were identified. Aspergillus species were isolated in 71% of episodes and anti-Aspergillus antibodies in 93%. Eleven episodes were breakthrough infections. Antifungal treatment was prolonged, with a median of 13 months, and 6 patients (7 episodes) required surgery, with a high rate of postsurgical complications. One patient died and 6 had a relapse.

CONCLUSIONS

Chronic and allergic forms of aspergillosis occurred in 17.5% of STAT3-deficient patients, mostly in lung cavities. Almost half had recurrences, despite prolonged antifungal treatment and/or surgery.

Для цитирования: Duréault Amélie, Tcherakian Colas, Poiree Sylvain, Catherinot Emilie, Danion François, Jouvion Grégory, Bougnoux Marie Elisabeth, Mahlaoui Nizar, Givel Claire, Castelle Martin, Picard Capucine, Chansdesris Marie Olivia, Lortholary Olivier, Lanternier Fanny, French Mycoses Study Group. Spectrum of Pulmonary Aspergillosis in Hyper-IgE Syndrome with Autosomal-Dominant STAT3 Deficiency.. The journal of allergy and clinical immunology. In practice. 2019. DOI: 10.1016/j.jaip.2019.02.041.

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