| Literature DB >> 28932715 |
Eloy E Ordaya1, Sulieman Abu Jarir2, Robert Yoo3, Pranatharthi H Chandrasekar4.
Abstract
INTRODUCTION: Hemophagocytic lymphohistiocytosis (HLH) is a clinical syndrome of hyperinflammation leading to an uncontrolled and ineffective immune response, associated with high mortality. CASE REPORT: A 26-year-old woman with acute lymphoblastic leukemia, 8 months in remission, was found to have HLH. Without any improvement, stem cell transplantation was considered. Then, Mycobacterium avium complex (MAC) infection was identified as cause of her HLH. With appropriate therapy for infection, HLH improved and transplantation was averted.Entities:
Keywords: Hemophagocytic lymphohistiocytosis; atypical mycobacteria; pancytopenia; unexplained fever
Year: 2017 PMID: 28932715 PMCID: PMC5601098 DOI: 10.18683/germs.2017.1120
Source DB: PubMed Journal: Germs ISSN: 2248-2997