Rare early hematogenous disseminated tuberculosis inducing hemophagocytic syndrome in conflict treatment

Abstract This article presents a case of an acute onset in a middle-aged male who exhibited persistent high fever (temperature > 40 °C), delirium, and respiratory distress. Initial chest CT only suggested "bilateral pneumonia," and empirical anti-infection treatment proved ineffective....

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Main Authors: Xiao-Hui Jin, Xin-Wei Shang, Hui-Qiang Zhang
Format: Article
Language:English
Published: BMC 2025-07-01
Series:BMC Infectious Diseases
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Online Access:https://doi.org/10.1186/s12879-025-11278-7
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author Xiao-Hui Jin
Xin-Wei Shang
Hui-Qiang Zhang
author_facet Xiao-Hui Jin
Xin-Wei Shang
Hui-Qiang Zhang
author_sort Xiao-Hui Jin
collection DOAJ
description Abstract This article presents a case of an acute onset in a middle-aged male who exhibited persistent high fever (temperature > 40 °C), delirium, and respiratory distress. Initial chest CT only suggested "bilateral pneumonia," and empirical anti-infection treatment proved ineffective. The patient subsequently developed pancytopenia, splenomegaly, and markedly elevated ferritin levels (848.90 μg/L). Bone marrow aspiration demonstrated hemophagocytic activity and granulomatous lesions. A positive TB-PCR, confirmed the diagnosis of early hematogenous disseminated tuberculosis complicated by the hemophagocytic syndrome (HLH). The patient's condition gradually improved Following, individualized anti-tuberculosis therapy and immunosuppressive treatment. The uniqueness of this case lies in two main aspects: (1) early imaging did not show typical miliary nodules, which could have led to misdiagnosis as common pneumonia; (2) the dissemination of tuberculosis and onset of HLH occurred almost simultaneously, creating a therapeutic dilemma. Although tuberculosis complicated by HLH is rare, it poses significant danger. The cornerstone of treatment is effective control of the tuberculosis infection while simultaneously suppressing the excessive immune response. This case highlights the importance of considering tuberculosis complicated by HLH in patients with recurrent fever and pulmonary infiltrates. Early diagnosis and prompt treatment are crucial for improving prognosis. The article also discusses the underlying pathogenesis, offering valuable insights for clinical practice.
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issn 1471-2334
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publishDate 2025-07-01
publisher BMC
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series BMC Infectious Diseases
spelling doaj-art-6f3c6a6eff034f0ca004ec8afa4c23782025-08-20T03:04:15ZengBMCBMC Infectious Diseases1471-23342025-07-0125111010.1186/s12879-025-11278-7Rare early hematogenous disseminated tuberculosis inducing hemophagocytic syndrome in conflict treatmentXiao-Hui Jin0Xin-Wei Shang1Hui-Qiang Zhang2The First Affiliated Hospital of Xinxiang Medical UniversityThe First Affiliated Hospital of Xinxiang Medical UniversityThe First Affiliated Hospital of Xinxiang Medical UniversityAbstract This article presents a case of an acute onset in a middle-aged male who exhibited persistent high fever (temperature > 40 °C), delirium, and respiratory distress. Initial chest CT only suggested "bilateral pneumonia," and empirical anti-infection treatment proved ineffective. The patient subsequently developed pancytopenia, splenomegaly, and markedly elevated ferritin levels (848.90 μg/L). Bone marrow aspiration demonstrated hemophagocytic activity and granulomatous lesions. A positive TB-PCR, confirmed the diagnosis of early hematogenous disseminated tuberculosis complicated by the hemophagocytic syndrome (HLH). The patient's condition gradually improved Following, individualized anti-tuberculosis therapy and immunosuppressive treatment. The uniqueness of this case lies in two main aspects: (1) early imaging did not show typical miliary nodules, which could have led to misdiagnosis as common pneumonia; (2) the dissemination of tuberculosis and onset of HLH occurred almost simultaneously, creating a therapeutic dilemma. Although tuberculosis complicated by HLH is rare, it poses significant danger. The cornerstone of treatment is effective control of the tuberculosis infection while simultaneously suppressing the excessive immune response. This case highlights the importance of considering tuberculosis complicated by HLH in patients with recurrent fever and pulmonary infiltrates. Early diagnosis and prompt treatment are crucial for improving prognosis. The article also discusses the underlying pathogenesis, offering valuable insights for clinical practice.https://doi.org/10.1186/s12879-025-11278-7Hematogenous disseminated pulmonary tuberculosisHemophagocytic syndromeCytokine stormImmunosuppressive therapy
spellingShingle Xiao-Hui Jin
Xin-Wei Shang
Hui-Qiang Zhang
Rare early hematogenous disseminated tuberculosis inducing hemophagocytic syndrome in conflict treatment
BMC Infectious Diseases
Hematogenous disseminated pulmonary tuberculosis
Hemophagocytic syndrome
Cytokine storm
Immunosuppressive therapy
title Rare early hematogenous disseminated tuberculosis inducing hemophagocytic syndrome in conflict treatment
title_full Rare early hematogenous disseminated tuberculosis inducing hemophagocytic syndrome in conflict treatment
title_fullStr Rare early hematogenous disseminated tuberculosis inducing hemophagocytic syndrome in conflict treatment
title_full_unstemmed Rare early hematogenous disseminated tuberculosis inducing hemophagocytic syndrome in conflict treatment
title_short Rare early hematogenous disseminated tuberculosis inducing hemophagocytic syndrome in conflict treatment
title_sort rare early hematogenous disseminated tuberculosis inducing hemophagocytic syndrome in conflict treatment
topic Hematogenous disseminated pulmonary tuberculosis
Hemophagocytic syndrome
Cytokine storm
Immunosuppressive therapy
url https://doi.org/10.1186/s12879-025-11278-7
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AT xinweishang rareearlyhematogenousdisseminatedtuberculosisinducinghemophagocyticsyndromeinconflicttreatment
AT huiqiangzhang rareearlyhematogenousdisseminatedtuberculosisinducinghemophagocyticsyndromeinconflicttreatment