Anjali V T, Rai Reena, Maheswari G Uma, Kumar Prasanna N
Department of Dermatology, PSG Institute of Medical Science and Research, Coimbatore, Tamil Nadu, India.
Department of Pathology, PSG Institute of Medical Science and Research, Coimbatore, Tamil Nadu, India.
Indian Dermatol Online J. 2020 Mar 9;11(2):219-221. doi: 10.4103/idoj.IDOJ_299_19. eCollection 2020 Mar-Apr.
Hemophagocytic syndrome or hemophagocytic lymphohistiocytosis (HLH) is a rare but potentially fatal disease caused by dysregulated activation of macrophages against one's blood cells. Major pathologic feature of HLH is hemophagocytosis. We present a case of HLH complicating methotrexate toxicity in a 65-year-old psoriatic patient with history of renal disease. Diagnosis of HLH was established as he fulfilled five out of eight HLH diagnostic criteria. This case report is presented to enlighten clinicians about the clinical entity of HLH and to suspect and recognize this rare and generally fatal disease at the earliest.
噬血细胞综合征或噬血细胞性淋巴组织细胞增生症(HLH)是一种罕见但可能致命的疾病,由巨噬细胞对自身血细胞的激活失调引起。HLH的主要病理特征是噬血细胞现象。我们报告一例65岁银屑病患者,有肾脏疾病史,发生HLH并发甲氨蝶呤中毒。由于该患者符合八项HLH诊断标准中的五项,故确诊为HLH。本病例报告旨在使临床医生了解HLH这一临床实体,并尽早怀疑和认识这种罕见且通常致命的疾病。