A HELLP syndrome complicates a gestational trophoblastic neoplasia in a perimenopausal woman: A case report

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Abstract

Background: HELLP syndrome is a combination of symptoms described as hemolysis, elevated liver enzymes and low platelets, that complicates 0.01-0.6 % of pregnancies. HELLP syndrome has been scarcely reported associated with partial moles, another rare complication of pregnancy. This manuscript describes the only reported case of HELLP syndrome associated with a complete invasive hydatiform mole. Case presentation: We report a perimenopausal patient in prolonged remission from an uncommon high-risk invasive complete mole. The diagnosis was set in a context of early onset preeclampsia and HELLP syndrome. The development of life-threatening complications required primary hysterectomy. Postoperative hCG quickly returned to normal with EMA/CO multi-agent chemotherapy. Conclusion: Our patient is in prolonged remission from a complete mole complicated with EOP and HELLP syndrome. This exceptional case of complicated gestational trophoblastic neoplasia reflects a very rare condition in which several risk factors for placental ischemia are associated. Emergency hysterectomy should be considered as salvage initial treatment in such life-threatening situations.

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APA

Vogin, G., Golfier, F., Hajri, T., Leroux, A., & Weber, B. (2016). A HELLP syndrome complicates a gestational trophoblastic neoplasia in a perimenopausal woman: A case report. BMC Cancer, 16(1). https://doi.org/10.1186/s12885-016-2641-2

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