A Case of DILI and Subsequent HLH Induced by Allopurinol

Edward Butt, Jaison John, Joseph Gosnell, Michael C. Boyars

Research output: Contribution to journalArticlepeer-review

Abstract

Hemophagocytic lymphohistiocytosis (HLH) is a syndrome that occurs because of uncontrolled immune cell activation and can present as a primary or acquired disorder. It is an illness with a high mortality rate that has been increasing in incidence over the past decade. There are few reports of allopurinol-induced HLH. This case describes a patient who was initially diagnosed with drug-induced liver injury secondary to allopurinol and subsequently diagnosed with HLH secondary to allopurinol. The discussion highlights the pathophysiology, clinical findings, diagnostic work-up, and treatment of HLH, along with mentioning interventions that focus on prevention of these diseases.

Original languageEnglish (US)
Article numbere220436
JournalAnnals of Internal Medicine Clinical Cases
Volume1
Issue number8
DOIs
StatePublished - Oct 2022
Externally publishedYes

Keywords

  • Allopurinol
  • Biopsy
  • Bone marrow
  • Death rates
  • Drugs
  • Etiology
  • Fevers
  • Hemorrhage
  • Liver
  • Serum glutamic oxaloacetic transaminase

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Internal Medicine
  • Clinical Biochemistry

Fingerprint

Dive into the research topics of 'A Case of DILI and Subsequent HLH Induced by Allopurinol'. Together they form a unique fingerprint.

Cite this