| Literature DB >> 36262481 |
David Masterman1, Sonal Gandhi1,2, Amteshwar Singh1,2, Tanmay Singh3, Ashampreet Kaur4.
Abstract
Hemophagocytic lymphohistiocytosis (HLH) is a rare systemic inflammatory disorder that is rapidly progressive and carries a poor prognosis. We present a case of HLH caused by undiagnosed B cell lymphoma, presenting initially with splenic infarction. Both HLH and splenic infarction are secondary conditions with a wide range of underlying etiologies. When either condition is identified, a prompt search for the underlying trigger is needed to prevent devastating consequences. We demonstrate the difficulties and barriers that can delay the diagnosis of HLH, and emphasize the importance of early treatment in improving survival rates.Entities:
Keywords: B cell lymphoma; H-score; Hemophagocytic lymphohistiocytosis (HLH); Splenic infarct
Year: 2022 PMID: 36262481 PMCID: PMC9529637 DOI: 10.55729/2000-9666.1097
Source DB: PubMed Journal: J Community Hosp Intern Med Perspect ISSN: 2000-9666