AI Article Synopsis

  • The text discusses Legionella infection, which can cause severe health issues ranging from mild flu-like symptoms to serious conditions like pneumonia and multi-organ failure, and may also be linked to rare blood disorders like immune thrombocytopenic purpura (ITP).
  • A case study is presented of a 53-year-old man who showed symptoms of pneumonia and severe low platelet count, which was later diagnosed as Legionella infection after positive urine antigen tests.
  • It emphasizes the importance of recognizing Legionella as a potential cause in patients with pneumonia and significant thrombocytopenia, as early detection can improve patient outcomes and prevent severe complications.

Article Abstract

Introduction: can cause a wide spectrum of clinical manifestations, ranging from a mild flu-like illness to fulminant multi-organ involvement, characterised by severe pneumonia, diarrhoea, encephalopathy, shock, hepatic dysfunction and renal failure. Very rarely, it can be associated with haematologic conditions such as thrombotic thrombocytopenic purpura (TTP), haemolytic uraemic syndrome (HUS) and immune thrombocytopenic purpura (ITP). We report a rare case of causing ITP and review previously published cases of thrombocytopenia associated with Legionellosis in the literature.

Case Description: A 53-year-old male presented with fevers, chills, a productive cough and severe haemoptysis. Blood work was remarkable for leukocytosis, severe thrombocytopenia and hyponatraemia. Computed tomography (CT) imaging showed left lower lobe lung consolidation, and a peripheral blood smear showed giant platelets consistent with ITP. Legionella urine antigen testing returned positive. He was treated with intravenous immunoglobin, steroid taper and a ten-day course of azithromycin, which led to normalisation of his platelet count and resolution of the pneumonia.

Discussion: can lead to complement-mediated destruction of platelets resulting in ITP. Antibodies against can also cross-react with the enzyme ADAMTS13, inhibiting its function and resulting in TTP and HUS. Additionally, can infect vascular endothelial cells causing their death and stimulating release of von Willebrand factor (vWF) multimers into the bloodstream, promoting thrombosis and platelet consumption.

Conclusion: It is important for internists to consider in the differential for any patient presenting with pneumonia and severe thrombocytopenia. Earlier detection and intervention can lead to prevention of critical bleeding and better outcomes.

Learning Points: is rarely associated with different haematologic disorders resulting in severe bleeding diathesis as well as thrombosis.It is important for internists to consider in the differential diagnosis for any patient presenting with pneumonia and severe thrombocytopenia.Earlier detection and intervention can lead to prevention of critical bleeding and better outcomes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11379109PMC
http://dx.doi.org/10.12890/2024_004817DOI Listing

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