1. Fatal autoimmune pneumonitis requiring bilobectomy and omental flap repair in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)
- Author
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Michail S. Lionakis, Jeffrey G. Walls, Huy M. Do, Stephanie A. Kubala, Elise M. N. Ferré, David S. Schrump, Kenneth N. Olivier, and Les R. Folio
- Subjects
Pulmonary and Respiratory Medicine ,medicine.medical_specialty ,animal structures ,Case Report ,medicine.disease_cause ,Immune tolerance ,Autoimmunity ,Immunomodulation ,Diseases of the respiratory system ,AIRE ,Bronchopleural fistula ,medicine ,APS-1 ,Pneumonitis ,Bronchiectasis ,RC705-779 ,business.industry ,Dystrophy ,Autoimmune polyendocrinopathy ,Autoimmune regulator ,medicine.disease ,Dermatology ,Omental flap repair ,Autoimmune pneumonitis ,Complication ,business ,APECED - Abstract
We present a severe case of progressive autoimmune pneumonitis requiring surgical intervention in a patient with the monogenic syndrome, autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED). APECED is caused by loss-of-function mutations in the autoimmune regulator (AIRE) gene, which lead to impaired central immune tolerance and autoimmune organ destruction including pneumonitis, an underrecognized, life-threatening complication. When clinicians evaluate patients with pneumonitis, recurrent mucosal candidiasis, and autoimmunity, APECED should be considered in the differential. Additionally, in patients with established APECED, a chest computed tomography is preferred to identify pneumonitis early on and to promptly initiate lymphocyte-directed immunomodulatory treatment, which can prevent irreversible lung destruction.
- Published
- 2021