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Life threatening chylothorax in a patient with congenital thrombophilia: case report.

Abstract
We reported here a case of bilateral chylothorax as a result of widespread thrombi formation in a patient who was heterozygote for factor V leiden gene mutation and who had antithrombin III deficiency. We performed bilateral chest tubes, thrombolytic and oral anticoagulant therapy. The patient responded to the therapy. She has been in follow up without symptoms for 18 months.
AuthorsGülay Ulusal Okyay, Ezgi Coşkun Yenigün, Gülbahar Darilmaz Yüce, I Safa Yildirim, Sadik Ardiç
JournalTuberkuloz ve toraks (Tuberk Toraks) Vol. 55 Issue 4 Pg. 404-8 ( 2007) ISSN: 0494-1373 [Print] Turkey
PMID18224511 (Publication Type: Case Reports, Journal Article)
Topics
  • Adolescent
  • Back Pain (etiology)
  • Chylothorax (complications, diagnosis, therapy)
  • Diagnosis, Differential
  • Dyspnea (etiology)
  • Factor V Deficiency (complications, congenital, diagnosis, therapy)
  • Female
  • Humans
  • Thrombophilia (complications, congenital, diagnosis, therapy)

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