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    Date Issued2008 (1)Author
    Angelis, Sheryn M. (1)
    Fraire, Armando E. (1)Kielbasa, Shasta (1)Libraty, Daniel H. (1)McNamee, Ciaran (1)View MoreUMass Chan AffiliationCenter for Infectious Disease and Vaccine Research (1)Department of Medicine (1)Department of Pathology (1)Document TypeJournal Article (1)KeywordLife Sciences (1)Medicine and Health Sciences (1)View MoreJournalJournal of medical case reports (1)

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    Lessons from Mycobacterium avium complex-associated pneumonitis: a case report

    Zota, Victor; Angelis, Sheryn M.; Fraire, Armando E.; McNamee, Ciaran; Kielbasa, Shasta; Libraty, Daniel H. (2008-05-15)
    ABSTRACT: INTRODUCTION: Mycobacterium avium complex (MAC) is an increasingly recognized cause of pulmonary disease in immunocompetent individuals. An acute form of MAC lung disease, MAC-associated pneumonitis, has generally been associated with the use of hot tubs. There is controversy in the literature about whether MAC-associated pneumonitis is a classic hypersensitivity pneumonitis or is a direct manifestation of mycobacterial infection. CASE PRESENTATION: We report the second case in the literature of MAC-associated pneumonitis not related to the use of hot tubs. The source of MAC in a 52-year-old immunocompetent patient was an intrapulmonary cyst containing numerous acid-fast bacilli. The patient developed disseminated miliary nodules throughout both lung fields. Histological examination of resected lung tissue revealed well-formed, acid-fast negative granulomas composed predominantly of CD4+ T-cells and CD68+ histiocytes. The granulomas were strongly positive for tumor necrosis factor-alpha, a pro-inflammatory cytokine. CONCLUSION: The attempt to classify MAC-associated pneumonitis as either a classic hypersensitivity pneumonitis or a direct manifestation of mycobacterial infection is not particularly useful. Our case demonstrates that MAC-associated pneumonitis is characterized by a vigorous T-helper 1-like, pro-inflammatory, immune response to pulmonary mycobacterial infection. The immunopathology provides a rationale for clinical studies of anti-MAC therapy with the addition of anti-inflammatory agents (for example, corticosteroids) to hasten the resolution of infection and symptoms.
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