A Fatal Etiology of Splenic Infarction.
J Community Hosp Intern Med Perspect
; 12(5): 78-83, 2022.
Article
em En
| MEDLINE
| ID: mdl-36262481
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.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Tipo de estudo:
Etiology_studies
/
Prognostic_studies
Idioma:
En
Revista:
J Community Hosp Intern Med Perspect
Ano de publicação:
2022
Tipo de documento:
Article
País de afiliação:
Estados Unidos