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A Rare Case of Chest Wall Abscess by Nocardia in a Patient With Sarcoidosis

Nocardia is a rare gram-positive pathogen reported to cause infections in immunocompromised individuals. It usually involves the lungs but may also lead to abscess formation; cases of disseminated nocardiosis have also been reported. We are presenting a case of an Asian male who had sarcoidosis with...

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Autores principales: Sana, Mahreen, Mahmood Butt, Faheem, Hasan, Muhammad Imran ul, Amir, Adnan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9366025/
https://www.ncbi.nlm.nih.gov/pubmed/35967147
http://dx.doi.org/10.7759/cureus.26769
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author Sana, Mahreen
Mahmood Butt, Faheem
Hasan, Muhammad Imran ul
Amir, Adnan
author_facet Sana, Mahreen
Mahmood Butt, Faheem
Hasan, Muhammad Imran ul
Amir, Adnan
author_sort Sana, Mahreen
collection PubMed
description Nocardia is a rare gram-positive pathogen reported to cause infections in immunocompromised individuals. It usually involves the lungs but may also lead to abscess formation; cases of disseminated nocardiosis have also been reported. We are presenting a case of an Asian male who had sarcoidosis with pulmonary and skin involvement. The patient was on long-term immunosuppressive therapy with corticosteroids with good control of the disease. He developed a fever, weight loss, and right-sided chest pain. CT of the chest showed new nodular infiltrates. Worsening of sarcoidosis was suspected; the corticosteroid dose was increased and methotrexate was started. There was no favorable response to the increase in immunosuppressive therapy. Weight loss was followed by worsening shortness of breath and fluctuant swelling in the right lateral half of the chest. Bronchoalveolar lavage was done to rule out tuberculosis but it did not show any organism’s growth. Ultrasound-guided needle aspiration from the abscess was done that showed growth of Nocardia species. Therapeutic dose co-trimoxazole (trimethoprim-sulphamethoxazole) was started as first-line therapy after confirming the organism’s drug susceptibility pattern along with needle aspiration of the collection on the chest wall. Immunosuppressive agents were stopped. There was a good response to treatment with resolution of symptoms within two months. However, complete radiological recovery took 10 months. Co-trimoxazole (trimethoprim-sulphamethoxazole) therapy continued for two months after radiological recovery. Physicians, therefore, should keep Nocardia as an important differential diagnosis while treating the immunosuppressed population.
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spelling pubmed-93660252022-08-12 A Rare Case of Chest Wall Abscess by Nocardia in a Patient With Sarcoidosis Sana, Mahreen Mahmood Butt, Faheem Hasan, Muhammad Imran ul Amir, Adnan Cureus Internal Medicine Nocardia is a rare gram-positive pathogen reported to cause infections in immunocompromised individuals. It usually involves the lungs but may also lead to abscess formation; cases of disseminated nocardiosis have also been reported. We are presenting a case of an Asian male who had sarcoidosis with pulmonary and skin involvement. The patient was on long-term immunosuppressive therapy with corticosteroids with good control of the disease. He developed a fever, weight loss, and right-sided chest pain. CT of the chest showed new nodular infiltrates. Worsening of sarcoidosis was suspected; the corticosteroid dose was increased and methotrexate was started. There was no favorable response to the increase in immunosuppressive therapy. Weight loss was followed by worsening shortness of breath and fluctuant swelling in the right lateral half of the chest. Bronchoalveolar lavage was done to rule out tuberculosis but it did not show any organism’s growth. Ultrasound-guided needle aspiration from the abscess was done that showed growth of Nocardia species. Therapeutic dose co-trimoxazole (trimethoprim-sulphamethoxazole) was started as first-line therapy after confirming the organism’s drug susceptibility pattern along with needle aspiration of the collection on the chest wall. Immunosuppressive agents were stopped. There was a good response to treatment with resolution of symptoms within two months. However, complete radiological recovery took 10 months. Co-trimoxazole (trimethoprim-sulphamethoxazole) therapy continued for two months after radiological recovery. Physicians, therefore, should keep Nocardia as an important differential diagnosis while treating the immunosuppressed population. Cureus 2022-07-12 /pmc/articles/PMC9366025/ /pubmed/35967147 http://dx.doi.org/10.7759/cureus.26769 Text en Copyright © 2022, Sana et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Sana, Mahreen
Mahmood Butt, Faheem
Hasan, Muhammad Imran ul
Amir, Adnan
A Rare Case of Chest Wall Abscess by Nocardia in a Patient With Sarcoidosis
title A Rare Case of Chest Wall Abscess by Nocardia in a Patient With Sarcoidosis
title_full A Rare Case of Chest Wall Abscess by Nocardia in a Patient With Sarcoidosis
title_fullStr A Rare Case of Chest Wall Abscess by Nocardia in a Patient With Sarcoidosis
title_full_unstemmed A Rare Case of Chest Wall Abscess by Nocardia in a Patient With Sarcoidosis
title_short A Rare Case of Chest Wall Abscess by Nocardia in a Patient With Sarcoidosis
title_sort rare case of chest wall abscess by nocardia in a patient with sarcoidosis
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9366025/
https://www.ncbi.nlm.nih.gov/pubmed/35967147
http://dx.doi.org/10.7759/cureus.26769
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