Abstract
Objectives: Haemophagocytic lymphohistiocytosis (HLH) is a potentially fatal disorder of the immune system that typically occurs in the paediatric population. Diagnosing this rare disease in the adult population is challenging, particularly during pregnancy.
Case presentation: We present a case of a gravid patient developing HLH at week 13 of gestation undergoing a medical termination of pregnancy at 27 weeks due to anhydramnios and associated stopped foetal growth.
Conclusions: Disease triggers could vary from a simple viral infection to the pregnancy as such causing the disorder. Treatment should benefit the mother and limit the foetal harm.
Case presentation: We present a case of a gravid patient developing HLH at week 13 of gestation undergoing a medical termination of pregnancy at 27 weeks due to anhydramnios and associated stopped foetal growth.
Conclusions: Disease triggers could vary from a simple viral infection to the pregnancy as such causing the disorder. Treatment should benefit the mother and limit the foetal harm.
Original language | English |
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Article number | 20210004 |
Journal | CASE REPORTS IN PERINATAL MEDICINE |
Volume | 11 |
Issue number | 1 |
DOIs | |
Publication status | Published - 27 Jan 2022 |
Bibliographical note
© 2022 Larissa Fávero Vanraes et al., published by De Gruyter, Berlin/Boston.Keywords
- anhydramnios
- haemophagocytic lymphohistiocytosis
- pregnancy