噬血作用
细胞减少
医学
妊娠期
肺结核
怀孕
全血细胞减少症
骨髓
胎儿
外科
内科学
儿科
病理
生物
遗传学
作者
Fernández Aa,de Velasco Pérez Df,Fournier Mc,Moreno Del Prado Jc,Torras Bp,Cañete Palomo Ml
标识
DOI:10.4103/ijmy.ijmy_14_17
摘要
Hemophagocytic syndrome is a life-threatening disease characterized by the uncontrolled activation of macrophages, resulting in hemophagocytosis of blood cells in the bone marrow. A 20-year-old gravida at 23-week and 5-day gestation was admitted to hospital to evaluate fever up to 104°F of unknown origin, moderate cytopenia, and elevated levels of liver enzymes. Bone marrow biopsy confirmed hemophagocytic syndrome, and polymerase chain reaction came back positive for Mycobacterium tuberculosis. Supportive care and tuberculosis treatment resulted in clinical improvement. At 27 weeks and 5 days, premature rupture of the membranes occurred, and because of the high probability of reactivating the hemophagocytic syndrome, a cesarean section was performed at 29-week and 2-day gestation. Hemophagocytic syndrome is an uncommon disease which rarely appears during pregnancy. Early diagnosis and treatment can save both maternal and fetal lives.
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