Cutaneous Tuberculosis in Heart Transplant.

Transplant Proc

Infectious Diseases Department, Centro Hospitalar Universitário de São João, Porto, Portugal; Faculty of Medicine, University of Porto, Porto, Portugal; ESCMID Study Group for Infections in Compromised Hosts, European Society of Clinical Microbiology and Infectious Diseases.

Published: November 2023

AI Article Synopsis

  • * A heart transplant recipient with disseminated TB presented with skin abscesses that were misdiagnosed as a bacterial infection, but the correct diagnosis was confirmed through specific testing for Mycobacterium tuberculosis.
  • * The patient experienced complications due to immune reconstitution inflammatory syndrome but improved significantly after adjusting treatment, showing a positive response to antituberculous therapy over six months.

Article Abstract

Tuberculosis is a disease with a significant global burden in terms of morbidity and mortality. It usually presents as a pulmonary disease but can occasionally have extrapulmonary presentations. Immunosuppressed people are at an increased risk of tuberculosis and more frequently have atypical manifestations of the disease. Cutaneous involvement is estimated to occur in only 2% of extrapulmonary presentations. We report a case of a heart transplant recipient with disseminated tuberculosis who initially presented with cutaneous manifestations in the form of multiple abscesses that were mistaken for a community-acquired bacterial infection. The diagnosis was made after positive nucleic acid amplification testing and cultures for Mycobacterium tuberculosis from the drainage of the abscesses. After initiating antituberculous treatment, the patient had 2 instances of immune reconstitution inflammatory syndrome. A combination of diminished immunosuppression due to discontinuation of mycophenolate mofetil in the setting of acute infection, rifampin drug interactions with cyclosporine, and the beginning of treatment of tuberculosis all contributed to this paradoxical worsening. The patient responded favorably to increased glucocorticoid therapy and showed no signs of treatment failure after 6 months of antituberculous therapy.

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Source
http://dx.doi.org/10.1016/j.transproceed.2023.03.041DOI Listing

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