Korean J Med > Volume 77(2); 2009 > Article
The Korean Journal of Medicine 2009;77(2):263-267.
A case of HELLP syndrome in a patient with complete hydatidyform mole
Eun-Mi Kim, Seok Hyun Kim, Jae Kyu Sung, Byung Seok Lee, Heon Young Lee, Young-Bok Ko, Kwang-Sun Suh
완전 포상기태에서 발생한 HELLP 증후군 1예
김은미, 김석현, 성재규, 이병석, 이헌영, 고영복, 서광선
Abstract
A 47-year-old woman was admitted to our emergency department with seizure and gross hematuria. Her blood pressure was 220/130 mmHg on admission. On abdominal examination, a firm mass reaching the umbilicus was felt arising from the pelvis. An ultrasound examination revealed a huge snow storm-appearing mass filling the uterine cavity but no fetus. Laboratory tests showed a high ß-hCG (>225,000 mU/mL), proteinuria (3+), elevated liver enzymes, low platelet count, and an abnormal peripheral blood smear. We diagnosed HELLP syndrome (hemolysis, elevated liver enzymes, and low platelets) with eclampsia in a patient with a complete hydatidiform mole. She underwent an emergency suction curettage for the hydatidiform mole. The liver enzymes and platelet count normalized about 2 weeks after the suction curettage. HELLP syndrome in a patient with hydatiform mole is very rare. Here, we report a patient who presented with a combination of HELLP syndrome, eclampsia, and a complete hydatidiform mole.
Key Words: HELLP syndrome; Eclampsia; Hydatidiform mole


TOOLS
METRICS Graph View
  • 1,474 View
  • 19 Download

Editorial Office
101-2501, Lotte Castle President, 109 Mapo-daero, Mapo-gu, Seoul 04146, Korea
Tel: +82-2-2271-6791    Fax: +82-2-790-0993    E-mail: kaim@kams.or.kr                

Copyright © 2024 by The Korean Association of Internal Medicine.

Developed in M2PI

Close layer
prev next