Postoperative pulmonary embolism in a young female accompanying with Factor V Leiden mutation and hereditary sypherocytosis

Karnak D., Beder S., KAYACAN O., Berk O.

JOURNAL OF THROMBOSIS AND THROMBOLYSIS, cilt.17, sa.3, ss.213-217, 2004 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 17 Sayı: 3
  • Basım Tarihi: 2004
  • Doi Numarası: 10.1023/b:thro.0000040491.79092.11
  • Dergi Adı: JOURNAL OF THROMBOSIS AND THROMBOLYSIS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.213-217
  • Anahtar Kelimeler: FVL mutation, anaemia, foetal loss, hereditary spherocytosis, DEEP-VEIN THROMBOSIS, ACTIVATED PROTEIN-C, VENOUS THROMBOEMBOLISM, INCREASED RISK, RESISTANCE, PREVALENCE, PREGNANCY, WOMEN, GENE, CARRIERS
  • Ankara Üniversitesi Adresli: Evet

Özet

A 20 year-old female, heterozygous for Factor V Leiden mutation (FVLM) is presented. Her personal history was prominent for severe anaemia during her gestation. Aetiology of anaemia was found to be hereditary spherocytosis (HS). Intrauterine foetal death had occurred at 20 weeks of gestational age. Two days after curettage, she developed pulmonary embolism ( PE). This is an unusual case of pulmonary embolism and intrauterine foetal death coexisting with FVLM and/or HS. We present the case so that a general practitioner or haematologist can hardly see such cases in daily practice. Hence, a young female with PE should be screened for hypercoagulable states including FVLM or HS.