Masterman David, Gandhi Sonal, Singh Amteshwar, Singh Tanmay, Kaur Ashampreet
Division of Hospital Medicine, Johns Hopkins Bayview Medical Center Baltimore, MD, USA.
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
J Community Hosp Intern Med Perspect. 2022 Sep 9;12(5):78-83. doi: 10.55729/2000-9666.1097. eCollection 2022.
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.
噬血细胞性淋巴组织细胞增生症(HLH)是一种罕见的系统性炎症性疾病,病情进展迅速,预后不良。我们报告一例由未确诊的B细胞淋巴瘤引起的HLH病例,最初表现为脾梗死。HLH和脾梗死均为继发病症,潜在病因广泛。当发现任何一种病症时,都需要迅速寻找潜在诱因以防止产生严重后果。我们展示了可能延迟HLH诊断的困难和障碍,并强调早期治疗对提高生存率的重要性。