Hindi Zakaria, Khaled Abdallah A, Abushahin Ashraf
Department of Internal Medicine, Texas Tech University Health Sciences Center at the Permian Basin, Odessa, TX, USA.
School of Medicine, The University of Jordan, Amman, Jordan.
SAGE Open Med Case Rep. 2017 Dec 17;5:2050313X17746309. doi: 10.1177/2050313X17746309. eCollection 2017.
Hemophagocytic syndrome or hemophagocytic lymphohistiocytosis is a rare condition characterized by excessive inflammation that is thought to be caused by the absence of normal downregulation of activated macrophages and lymphocytes. The treatment of hemophagocytic lymphohistiocytosis can depend on whether it is primary or secondary. In secondary hemophagocytic lymphohistiocytosis, the treatment can be directed according to the cause. In general, protocol HLH-94 (which consists of dexamethasone and etoposide in induction and maintenance) has been widely used as it has good outcomes. Hemophagocytic lymphohistiocytosis and septic shock largely overlap which can lead to refractory septic shock and death if not treated. Unfortunately, there is no clear approach for such dilemma. Thereby, we would like to present our case as it has a valuable approach to hemophagocytic lymphohistiocytosis in the setting of sepsis.
A 60-year-old female, with history of hypertension, came with fever, productive cough, and dyspnea; she was admitted for acute exacerbation of chronic obstructive pulmonary disease and was transferred to intensive care unit for septic shock. The patient progressed to refractory septic shock with no focus of infection. After further investigations, detailed history raised the suspicion of hemophagocytic lymphohistiocytosis; a bone marrow biopsy was collected and confirmed the diagnosis. The patient was on methylprednisolone while waiting for other investigation results and improved markedly. After ruling out secondary causes of hemophagocytic lymphohistiocytosis, she was switched to protocol-94 and continued to improve.
It should be emphasized that septic shock, with or without focus of infection, overlaps with hemophagocytic lymphohistiocytosis and can consequently lead to refractory septic shock and death. Thus, our aim of this case is to encourage further investigations, specifically for hemophagocytic lymphohistiocytosis in the setting of septic shock of unknown origin, to decrease mortality rate. More importantly, early initiation of immunosuppression therapy may be a crucial step before switching to hemophagocytic lymphohistiocytosis-specific treatment.
噬血细胞综合征或噬血细胞性淋巴组织细胞增生症是一种罕见病症,其特征为过度炎症反应,被认为是由活化巨噬细胞和淋巴细胞缺乏正常下调机制所致。噬血细胞性淋巴组织细胞增生症的治疗取决于其为原发性还是继发性。在继发性噬血细胞性淋巴组织细胞增生症中,治疗可根据病因进行。总体而言,方案HLH - 94(诱导期和维持期使用地塞米松和依托泊苷)因其良好疗效而被广泛应用。噬血细胞性淋巴组织细胞增生症与感染性休克在很大程度上重叠,如果不进行治疗,可能导致难治性感染性休克和死亡。不幸的是,对于这种困境尚无明确的解决方法。因此,我们想介绍我们的病例,因为它为脓毒症背景下的噬血细胞性淋巴组织细胞增生症提供了一种有价值的方法。
一名60岁女性,有高血压病史,因发热、咳痰和呼吸困难前来就诊;她因慢性阻塞性肺疾病急性加重入院,并因感染性休克转入重症监护病房。患者进展为难治性感染性休克,未发现感染病灶。经过进一步检查,详细病史引发了对噬血细胞性淋巴组织细胞增生症的怀疑;采集骨髓活检并确诊。患者在等待其他检查结果期间接受甲泼尼龙治疗,病情明显改善。在排除噬血细胞性淋巴组织细胞增生症的继发性病因后,她改用方案 - 94并持续好转。
应强调的是,无论有无感染病灶,感染性休克与噬血细胞性淋巴组织细胞增生症重叠,可能导致难治性感染性休克和死亡。因此,我们此病例的目的是鼓励进一步检查,特别是针对不明原因感染性休克背景下的噬血细胞性淋巴组织细胞增生症,以降低死亡率。更重要的是,在改用噬血细胞性淋巴组织细胞增生症特异性治疗之前,早期启动免疫抑制治疗可能是关键步骤。