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Sarcoidosis with marked necrosis in enlarged lymph nodes mimics mycobacterial infection: a case report

BACKGROUND: Sarcoidosis is pathologically characterized by the formation of non-necrotizing epithelioid cell granulomas. However, pathological findings of patients with sarcoidosis have rarely revealed necrosis. We report here on a patient with sarcoidosis which needed to be distinguished from infec...

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Autores principales: Miyashita, Yosuke, Hara, Munechika, Iwakami, Shin-ichiro, Matsuda, Hironari, Iwakami, Naoko, Takahashi, Kazuhisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053279/
https://www.ncbi.nlm.nih.gov/pubmed/33865452
http://dx.doi.org/10.1186/s13256-021-02797-3
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author Miyashita, Yosuke
Hara, Munechika
Iwakami, Shin-ichiro
Matsuda, Hironari
Iwakami, Naoko
Takahashi, Kazuhisa
author_facet Miyashita, Yosuke
Hara, Munechika
Iwakami, Shin-ichiro
Matsuda, Hironari
Iwakami, Naoko
Takahashi, Kazuhisa
author_sort Miyashita, Yosuke
collection PubMed
description BACKGROUND: Sarcoidosis is pathologically characterized by the formation of non-necrotizing epithelioid cell granulomas. However, pathological findings of patients with sarcoidosis have rarely revealed necrosis. We report here on a patient with sarcoidosis which needed to be distinguished from infectious disease because of marked necrosis in the lymph nodes. CASE PRESENTATION: A 46-year-old Japanese woman was referred to our hospital due to a dry cough and appetite loss. A chest X-ray and computed tomography revealed markedly enlarged mediastinal and hilar lymph nodes and hepatosplenomegaly. Surgical biopsy of these lymph nodes was performed in order to make a diagnosis. Pathological findings revealed epithelioid cell granuloma with marked necrosis that suggested infectious etiology such as mycobacterial and fungal infections. In addition to the pathological findings, immunoglobulin A (IgA) antibody for Mycobacterium avium complex (MAC), enlargement of lymph nodes and hepatosplenomegaly indicated disseminated MAC, while sarcoidosis was considered as another important differential diagnosis according to elevated angiotensin-converting enzyme, soluble interleukin-2 receptor and uveitis. While waiting for the results of the cultures of acid-fast bacilli, the symptoms of cough and consumption had worsened, and initiation of therapy was required before the confirmed diagnosis. The therapy for MAC was initiated because it was feared that immunosuppressive therapy containing corticosteroid for sarcoidosis could worsen the patient’s condition if MAC infection was the main etiology. However, the treatment for MAC was not effective, and it was clarified that no acid-fast bacilli were cultured in the liquid culture medium, so the diagnosis was corrected to sarcoidosis after reconsideration of clinical and pathological findings. Prednisolone (30 mg/day) was administered orally, and the patient’s symptoms and radiological findings improved. CONCLUSION: Sarcoidosis must be considered even if pathological findings reveal marked necrosis, because rare cases of sarcoidosis exhibit extensive necrosis in lymph nodes. It is extremely important to carefully examine the clinical and pathological findings through discussion with the examining pathologist to reach the correct diagnosis.
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spelling pubmed-80532792021-04-19 Sarcoidosis with marked necrosis in enlarged lymph nodes mimics mycobacterial infection: a case report Miyashita, Yosuke Hara, Munechika Iwakami, Shin-ichiro Matsuda, Hironari Iwakami, Naoko Takahashi, Kazuhisa J Med Case Rep Case Report BACKGROUND: Sarcoidosis is pathologically characterized by the formation of non-necrotizing epithelioid cell granulomas. However, pathological findings of patients with sarcoidosis have rarely revealed necrosis. We report here on a patient with sarcoidosis which needed to be distinguished from infectious disease because of marked necrosis in the lymph nodes. CASE PRESENTATION: A 46-year-old Japanese woman was referred to our hospital due to a dry cough and appetite loss. A chest X-ray and computed tomography revealed markedly enlarged mediastinal and hilar lymph nodes and hepatosplenomegaly. Surgical biopsy of these lymph nodes was performed in order to make a diagnosis. Pathological findings revealed epithelioid cell granuloma with marked necrosis that suggested infectious etiology such as mycobacterial and fungal infections. In addition to the pathological findings, immunoglobulin A (IgA) antibody for Mycobacterium avium complex (MAC), enlargement of lymph nodes and hepatosplenomegaly indicated disseminated MAC, while sarcoidosis was considered as another important differential diagnosis according to elevated angiotensin-converting enzyme, soluble interleukin-2 receptor and uveitis. While waiting for the results of the cultures of acid-fast bacilli, the symptoms of cough and consumption had worsened, and initiation of therapy was required before the confirmed diagnosis. The therapy for MAC was initiated because it was feared that immunosuppressive therapy containing corticosteroid for sarcoidosis could worsen the patient’s condition if MAC infection was the main etiology. However, the treatment for MAC was not effective, and it was clarified that no acid-fast bacilli were cultured in the liquid culture medium, so the diagnosis was corrected to sarcoidosis after reconsideration of clinical and pathological findings. Prednisolone (30 mg/day) was administered orally, and the patient’s symptoms and radiological findings improved. CONCLUSION: Sarcoidosis must be considered even if pathological findings reveal marked necrosis, because rare cases of sarcoidosis exhibit extensive necrosis in lymph nodes. It is extremely important to carefully examine the clinical and pathological findings through discussion with the examining pathologist to reach the correct diagnosis. BioMed Central 2021-04-18 /pmc/articles/PMC8053279/ /pubmed/33865452 http://dx.doi.org/10.1186/s13256-021-02797-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Miyashita, Yosuke
Hara, Munechika
Iwakami, Shin-ichiro
Matsuda, Hironari
Iwakami, Naoko
Takahashi, Kazuhisa
Sarcoidosis with marked necrosis in enlarged lymph nodes mimics mycobacterial infection: a case report
title Sarcoidosis with marked necrosis in enlarged lymph nodes mimics mycobacterial infection: a case report
title_full Sarcoidosis with marked necrosis in enlarged lymph nodes mimics mycobacterial infection: a case report
title_fullStr Sarcoidosis with marked necrosis in enlarged lymph nodes mimics mycobacterial infection: a case report
title_full_unstemmed Sarcoidosis with marked necrosis in enlarged lymph nodes mimics mycobacterial infection: a case report
title_short Sarcoidosis with marked necrosis in enlarged lymph nodes mimics mycobacterial infection: a case report
title_sort sarcoidosis with marked necrosis in enlarged lymph nodes mimics mycobacterial infection: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053279/
https://www.ncbi.nlm.nih.gov/pubmed/33865452
http://dx.doi.org/10.1186/s13256-021-02797-3
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