International Journal of Mycobacteriology (Jan 2017)

Hemophagocytic syndrome secondary to tuberculosis at 24-week gestation

  • Alexandra Arteaga Fernández,
  • David Fernández de Velasco Pérez,
  • M C. Jiménez Fournier,
  • J C Moreno del Prado,
  • B Paraíso Torras,
  • M L Cañete Palomo

DOI
https://doi.org/10.4103/ijmy.ijmy_14_17
Journal volume & issue
Vol. 6, no. 1
pp. 108 – 110

Abstract

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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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