scholarly journals Post Operative Chylothorax Development is Associated with Increased Incidence and Risk Profile for Central Venous Thrombosis

2007 ◽  
Author(s):  
Michael Andrew McCulloch
Keyword(s):  
Venous Thrombosis ◽  
Risk Profile ◽  
Central Venous ◽  
Central Venous Thrombosis

scholarly journals Central venous thrombosis and perioperative vascular access in adult intestinal transplantation †

2012 ◽  
Vol 108 (5) ◽  
pp. 776-783 ◽  
Author(s):  
T. Matsusaki ◽  
T. Sakai ◽  
C.D. Boucek ◽  
K. Abu-Elmagd ◽  
L.M. Martin ◽  
...  
Keyword(s):  
Venous Thrombosis ◽  
Vascular Access ◽  
Intestinal Transplantation ◽  
Central Venous ◽  
Central Venous Thrombosis

Chylothorax following apparently spontaneous central venous thrombosis in a patient with septic shock

2003 ◽  
Vol 35 (3) ◽  
pp. 230-233 ◽  
Author(s):  
John W. Berkenbosch ◽  
Philip M. Monteleone ◽  
Joseph D. Tobias
Keyword(s):  
Septic Shock ◽  
Venous Thrombosis ◽  
Central Venous ◽  
Central Venous Thrombosis

scholarly journals Hypofibrinogenaemia: A Case of Spontaneous Bleeding and Central Venous Thrombosis in the Same Lifetime

2020 ◽  
Author(s):  
Adriana Watts Soares ◽  
Maria Maia ◽  
João Espirito Santo ◽  
Ana Palricas Costa ◽  
Artur Pereira ◽  
...  
Keyword(s):  
Venous Thrombosis ◽  
Protein S ◽  
Pathogenic Mutation ◽  
Central Venous ◽  
Spontaneous Bleeding ◽  
Thrombotic Risk ◽  
Risk Pregnancy ◽  
S Deficiency ◽  
Central Venous Thrombosis ◽  
Life Threatening

The authors present the case of a 27-year-old patient who suffered from spontaneous bleeding during infancy and from a severe and central venous thrombosis in adult years. The patient underwent a thorough laboratory work-up on both occasions and was diagnosed with hypofibrinogenaemia as well as protein S deficiency, 2 diseases that contrast in their intrinsic bleeding/thrombotic risk. The patient´s high-risk pregnancy was carried out up to a successful full-term eutocic delivery which required fibrinogen concentrate to reduce life-threatening bleeding. The patient´s child was also diagnosed with hypofibrinogenaemia, later on confirmed with the pathogenic mutation Fibrinogen Marseilles II. This case was used to conduct a literature review of congenital fibrinogen disorders, rare entities that require more awareness for early diagnosis and accurate management.

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