Pregled bibliografske jedinice broj: 479659
Contraception-Related Deep Venous Thrombosis and Pulmonary Embolism in a 17-Year-Old Girl Heterozygous for Factor V Leiden, Prothrombin G20210A Mutation, MTHFR C677T and Homozygous for PAI-1 Mutation: Report of a Family with Multiple Genetic Risk Factors and Review of the Literature
Contraception-Related Deep Venous Thrombosis and Pulmonary Embolism in a 17-Year-Old Girl Heterozygous for Factor V Leiden, Prothrombin G20210A Mutation, MTHFR C677T and Homozygous for PAI-1 Mutation: Report of a Family with Multiple Genetic Risk Factors and Review of the Literature // Pathophysiology of haemostasis and thrombosis, 37 (2010), 1; 24-29 doi:10.1159/000319051 (međunarodna recenzija, članak, znanstveni)
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Naslov
Contraception-Related Deep Venous Thrombosis and
Pulmonary Embolism in a 17-Year-Old Girl
Heterozygous for Factor V Leiden, Prothrombin
G20210A Mutation, MTHFR C677T and Homozygous for
PAI-1 Mutation: Report of a Family with Multiple
Genetic Risk Factors and Review of the Literature
Autori
Leniček Krleza, Jasna ; Jakovljević, Gordana ; Bronić, Ana ; Coen Herak, Desiree ; Bonevski, Aleksandra ; Stepan-Giljević, Jasminka ; Roić, Goran
Izvornik
Pathophysiology of haemostasis and thrombosis (1424-8832) 37
(2010), 1;
24-29
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
deep venous thrombosis ; pulmonary embolism ; oral contraceptives ; teenagers ; prothrombotic risk factors
Sažetak
We present the case of a 17-year-old girl who suddenly woke up with localized pain in the left groin and the inability to twist her leg. After comprehensive physician and laboratory examinations, deep venous thrombosis with consequent pulmonary embolism was ascertained. She had not experienced any recent trauma, but she had started to take oral contraceptives 6 months prior to the onset of the symptoms. Her parents and sisters had been asymptomatic throughout their lives, but the family history revealed a few thromboembolic accidents. Using DNA analysis, heterozygosity for factor V Leiden, prothrombin gene mutation G20210A and methylenetetrahydrofolate reductase C677T, as well as the homozygous 4G/4G genotype in the plasminogen activator inhibitor 1 were identified in our patient. Subsequently, DNA analysis was performed in all living family members, and multiple factors associated with thrombophilia were discovered. Our case confirms the multifactorial cause of thromboembolic events and emphasizes the importance of oral contraceptive use in the onset of venous thrombosis, especially in teenage females. In addition, this case indicates that teenage females with a family history of thrombosis who are making choices about contraception could most likely benefit from advanced thrombophilia testing.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
MZOS-098-0982464-3120 - Farmakogenetika u dječjoj onkologiji (Stepan Giljević, Jasminka, MZOS ) ( CroRIS)
Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta,
Institut "Ruđer Bošković", Zagreb,
Klinički bolnički centar Zagreb
Profili:
Aleksandra Bonevski
(autor)
Jasminka Stepan Giljević
(autor)
Jasna Leniček Krleža
(autor)
Goran Roić
(autor)
Ana Bronić
(autor)
Gordana Jakovljević
(autor)
Poveznice na cjeloviti tekst rada:
Pristup cjelovitom tekstu rada doi content.karger.com www.ncbi.nlm.nih.govCitiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
Uključenost u ostale bibliografske baze podataka::
- EMBASE (Excerpta Medica)
- MEDLINE