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Case Reports
. 2013 Mar 1:2013:bcr2013008743.
doi: 10.1136/bcr-2013-008743.

Haemophagocytic syndrome with disseminated intravascular coagulation associated with tuberculosis

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Case Reports

Haemophagocytic syndrome with disseminated intravascular coagulation associated with tuberculosis

Eya Cherif et al. BMJ Case Rep. .

Abstract

Haemophagocytic syndrome (HPS) is a clinical entity that combines non-specific clinical and biological features. The diagnosis is usually confirmed by a bone marrow examination. HPS may be primary or secondary to a malignancy or to an infectious or autoimmune disease. Early aggressive survey of the aetiology and optimal treatment of the underlying disease improve the outcome of life-threatening HPS. Infection-associated HPS occurs predominantly in immunocompromised patients and is usually fatal. Leading trigger agents are viruses, especially the Epstein-Barr virus and cytomegalovirus. Mycobacterial infections associated with HPS are rare but should be considered in those patients where there is associated fever of unknown origin. We present a case of disseminated tuberculosis-associated HPS.

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Figures

Figure 1
Figure 1
CT of the chest demonstrates bilateral diffuse infiltrates of lungs.

References

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