Macrophage Activation Syndrome Discovered During Pregnancy: Case Report

M. Serraj Andaloussi, Hayat Midyani, C. Khalloufi, A. Lamrissi, K. Fichtali, S. Bouhya, Salah Hayar, Ihsane Moussaid, S. El Youssoufi, S. Salmi
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Abstract

Macrophage activation syndrome (MAS) or Haemophagocytic syndrome (HPS) results from an inappropriate stimulation of macrophages in bone marrow and lymphoid organs, leading to haemophagocytosis and hypercytokinemia. HPS may be primitive, essentially in pediatric population, or secondary to malignancy, infection or autoimmune disease. This disease is rare and prognosis is poor. The diagnosis of hemophagocytic syndrome remains a challenge especially during pregnancy. We report a case collected at the Elharouchimaternity service, taken in charge jointly with its intensive care unit, of a 26-year-old patient with no pathological history leading to an unsuccessful pregnancy presumed at 5 months in whom the MAS syndrome was retained due to pancytopenia. , hyperferitinemia, hypertriglyceridemia with the presence of a few hemophagocytes in the myelogram with a good evolution under bolus of solumedrol and symptomatic treatment. We discuss through this case the diagnostic difficulties, the obstetric complications as well as the options therapeutic.
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妊娠期发现巨噬细胞激活综合征:病例报告
巨噬细胞激活综合征(Macrophage activation syndrome, MAS)或噬血细胞综合征(Haemophagocytic syndrome, HPS)是由于骨髓和淋巴器官中巨噬细胞受到不适当的刺激,导致噬血细胞增多和高细胞因子血症。HPS可能是原始的,主要发生在儿科人群中,也可能继发于恶性肿瘤、感染或自身免疫性疾病。本病罕见,预后差。噬血细胞综合征的诊断仍然是一个挑战,特别是在怀孕期间。我们报告一个病例收集在elharouchem产科服务,联合负责其重症监护病房,一个26岁的患者没有病理史导致妊娠失败推定在5个月,MAS综合征保留由于全血细胞减少症。高铁血症、高甘油三酯血症,骨髓图中有少量噬血细胞,在静脉注射和对症治疗下进展良好。我们通过这个病例讨论诊断困难,产科并发症以及治疗的选择。
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