Severe hepatitis and pure red cell aplasia in adult Still's disease: good response to immunosuppressive therapy

H L Janssen, J M van Laar, B van Hoek, G J den Ottolander, J H van Krieken, F C Breedveld

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Adult-onset Still's disease is a systemic inflammatory disorder with a highly variable clinical course. Mild hepatitis and anemia are common manifestations. We describe a patient with adult Still's disease who developed a severe hepatitis and a life-threatening pure red cell aplasia. The hepatitis developed after treatment with NSAIDs was started. The patient was successfully treated with a combination of prednisone, cyclosporin, and methotrexate. Physicians should be aware that severe hepatitis and pure red cell aplasia can occur in adult Still's disease. We recommend a careful monitoring of liver functions in patients with adult Still's disease who are being treated with NSAIDs.

Original languageEnglish
Pages (from-to)1639-42
Number of pages4
JournalDigestive Diseases and Sciences
Volume44
Issue number8
Publication statusPublished - Aug 1999
Externally publishedYes

Keywords

  • Adult
  • Anti-Inflammatory Agents
  • Cyclosporine
  • Female
  • Hepatitis
  • Humans
  • Immunosuppression
  • Immunosuppressive Agents
  • Methotrexate
  • Prednisone
  • Red-Cell Aplasia, Pure
  • Still's Disease, Adult-Onset
  • Case Reports
  • Journal Article

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