Sternal Osteomyelitis Caused by Mycobacterium tuberculosis in a Heart Transplant Patient

Mycobacterium tuberculosis (MT) infection poses a significant risk in immunocompromised individuals, particularly in areas with high MT prevalence. We describe the case of a 43-year-old heart transplant recipient who developed chronic sternal wound secretion post-transplant surgery. Imaging revealed signs of inflammatory tissue suggestive of chronic osteomyelitis. Removal of the sternal wires was performed, followed by biopsy, which identified granulomatous inflammatory tissue and Langhans cells, that led to the diagnosis of MT infection later confirmed in culture results. The patient completed a 6-month tetraconjugate antituberculous therapy, resulting in successful wound healing and infection resolution. Atypical extrapulmonary MT manifestations require high clinical suspicion, especially in immunocompromised patients, to ensure timely diagnosis and treatment with favorable outcomes.

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Publication Details

Journal
JACC Case Reports
Published
2025-03-01
DOI
https://doi.org/10.1016/j.jaccas.2024.103088
Primary Topic
Infectious Diseases and Tuberculosis
Type
article
Field-Weighted Citation Impact
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article

Sternal Osteomyelitis Caused by Mycobacterium tuberculosis in a Heart Transplant Patient

Carballo Hernandez, Fernán Mendoza Beltrán, Carlos Orozco, William M Rios et al.
JACC Case Reports
Infectious Diseases and Tuberculosis
article

Sternal Osteomyelitis Caused by Mycobacterium tuberculosis in a Heart Transplant Patient

Carballo Hernandez, Fernán Mendoza Beltrán, Carlos Orozco, William M Rios, David Alberto Ocampo
article en

Abstract

Mycobacterium tuberculosis (MT) infection poses a significant risk in immunocompromised individuals, particularly in areas with high MT prevalence. We describe the case of a 43-year-old heart transplant recipient who developed chronic sternal wound secretion post-transplant surgery. Imaging revealed signs of inflammatory tissue suggestive of chronic osteomyelitis. Removal of the sternal wires was performed, followed by biopsy, which identified granulomatous inflammatory tissue and Langhans cells, that led to the diagnosis of MT infection later confirmed in culture results. The patient completed a 6-month tetraconjugate antituberculous therapy, resulting in successful wound healing and infection resolution. Atypical extrapulmonary MT manifestations require high clinical suspicion, especially in immunocompromised patients, to ensure timely diagnosis and treatment with favorable outcomes.

JACC Case ReportsVol. 30(5)
Universidad El Bosque (CO), Asociación Colombiana de Gastroenterología (CO)
Good health and well-being
Openalex Percentile: Top 93%
Infectious Diseases and Tuberculosis
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