Literature DB >> 3134883

Disseminated tuberculosis complicated by the hemophagocytic syndrome.

P J Browett1, A R Varcoe, A G Fraser, R B Ellis-Pegler.   

Abstract

A 43-year-old Polynesian presented with fever, abnormal liver function tests, bilateral pulmonary infiltrates, and a progressive neutropenia and thrombocytopenia. Bone marrow examination showed extensive and striking hemophagocytosis which raised the diagnosis of malignant histiocytosis. Mycobacterium tuberculosis was subsequently cultured from both urine and bone marrow. Hemophagocytosis is now a recognised association of several infections and we draw attention to this finding, particularly as the confident exclusion of malignancy can be very difficult and management is obviously very different.

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Year:  1988        PMID: 3134883     DOI: 10.1111/j.1445-5994.1988.tb02250.x

Source DB:  PubMed          Journal:  Aust N Z J Med        ISSN: 0004-8291


  4 in total

1.  Haemophagocytic lymphohistiocytosis: a cause for rare but fatal outcome in tuberculosis.

Authors:  Puneet Aggarwal; Gunjan Kumar; Nishanth Dev; Pushpa Kumari
Journal:  BMJ Case Rep       Date:  2012-09-30

2.  Pediatric hemophagocytic syndromes: a diagnostic and therapeutic challenge.

Authors:  Nada Jabado; Christine McCusker; Genevieve de Saint Basile
Journal:  Allergy Asthma Clin Immunol       Date:  2005-12-15       Impact factor: 3.406

3.  Thrombocytopenic purpura as a presenting manifestation of tubercular lymphadenitis.

Authors:  Sameer Bakhshi; Madhulika Kabra; Venkaleswaran K Iyer; L S Arya
Journal:  Indian J Pediatr       Date:  2003-12       Impact factor: 1.967

4.  Immune thrombocytopenic purpura associated with pulmonary tuberculosis.

Authors:  Tapan Das Bairagya; Sibes Kumar Das; Pulak Kumar Jana; Somnath Bhattacharya
Journal:  J Glob Infect Dis       Date:  2012-07
  4 in total

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