Immune thrombocytopenic purpura secondary to Helicobacter pylori.

Immune thrombocytopenic purpura is a disorder characterized by decreased platelet count that may be secondary to infectious or autoimmune etiologies. We present a patient with upper gastrointestinal bleeding complicated by severe thrombocytopenia. Endoscopy revealed gastritis with pathology positive...

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Publicado en:Baylor University Medical Center Proceedings Vol. 35; no. 1; pp. 60 - 62
Autores principales: Ramachandran, Lintu, Baloch, Luqman, Djirdeh, Taha Mohamed, Sidhu, Yadwinder, Gentile, Nicole, Affinati, Mario
Formato: case study pictorial Journal Article
Publicado: Taylor & Francis Ltd Jan2022
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jan2022
      vid: 35
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      pub: Taylor & Francis Ltd
      place: Philadelphia, Pennsylvania
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        10.1080/08998280.2021.1973293
        154224298
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        atl: Immune thrombocytopenic purpura secondary to Helicobacter pylori.
      aug:
        au:
          Ramachandran, Lintu
          Baloch, Luqman
          Djirdeh, Taha Mohamed
          Sidhu, Yadwinder
          Gentile, Nicole
          Affinati, Mario
        affil: Department of Internal Medicine, Mercyhealth, Rockford, Illinois
      sug:
        subj:
          Purpura, Thrombocytopenic Complications
          Helicobacter Pylori
          Blood Platelets Pathology
          Gastrointestinal Hemorrhage Complications
          Thrombocytopenia
          Endoscopy
          Gastritis
          Helicobacter Pylori Metabolism
          Antibiotics Therapeutic Use
          Diagnosis, Differential
          Adult
          Male
          Hematemesis
          Adult: 19-44 years
          Male
      ab: Immune thrombocytopenic purpura is a disorder characterized by decreased platelet count that may be secondary to infectious or autoimmune etiologies. We present a patient with upper gastrointestinal bleeding complicated by severe thrombocytopenia. Endoscopy revealed gastritis with pathology positive for Helicobacter pylori. Platelet count normalized after triple antibiotic therapy. The precise mechanism by which H. pylori causes immune thrombocytopenic purpura remains unclear; however, there are several plausible mechanisms. This case highlights the importance of keeping H. pylori in the differential in patients presenting with thrombocytopenia.
      pubtype: Academic Journal
      doctype:
        case study
        pictorial
        Journal Article
      ougenre: Article
    language: English
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