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Portal vein thrombosis with ruptured oesophageal varices as presenting manifestation of hereditary protein C deficiency.
The protein C system is essential in limiting the activation of coagulation in vivo. We report the case of a 45 year old man with portal vein thrombosis complicated by ruptured oesophageal varices. Low concentration of plasma protein C was found in the patient and subsequently in one brother with a...
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| Формат: | Статья |
| Язык: | English |
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1988
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| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1433741/ https://ncbi.nlm.nih.gov/pubmed/3384371 |
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pubmed-14337412007-06-11 Portal vein thrombosis with ruptured oesophageal varices as presenting manifestation of hereditary protein C deficiency. Valla, D Denninger, M H Delvigne, J M Rueff, B Benhamou, J P Gut Research Article The protein C system is essential in limiting the activation of coagulation in vivo. We report the case of a 45 year old man with portal vein thrombosis complicated by ruptured oesophageal varices. Low concentration of plasma protein C was found in the patient and subsequently in one brother with a history of venous thromboembolism, and also in one son and one nephew who were asymptomatic. Hereditary protein C deficiency should be considered in patients with portal hypertension due to portal vein thrombosis. 1988-06 /pmc/articles/PMC1433741/ /pubmed/3384371 Text en |
| institution |
US National Library of Medicine |
| collection |
PubMed Central |
| language |
English |
| format |
Article |
| topic |
Research Article |
| spellingShingle |
Research Article Valla, D Denninger, M H Delvigne, J M Rueff, B Benhamou, J P Portal vein thrombosis with ruptured oesophageal varices as presenting manifestation of hereditary protein C deficiency. |
| description |
The protein C system is essential in limiting the activation of coagulation in vivo. We report the case of a 45 year old man with portal vein thrombosis complicated by ruptured oesophageal varices. Low concentration of plasma protein C was found in the patient and subsequently in one brother with a history of venous thromboembolism, and also in one son and one nephew who were asymptomatic. Hereditary protein C deficiency should be considered in patients with portal hypertension due to portal vein thrombosis. |
| author |
Valla, D Denninger, M H Delvigne, J M Rueff, B Benhamou, J P |
| author_facet |
Valla, D Denninger, M H Delvigne, J M Rueff, B Benhamou, J P |
| author_sort |
Valla, D |
| title |
Portal vein thrombosis with ruptured oesophageal varices as presenting manifestation of hereditary protein C deficiency. |
| title_short |
Portal vein thrombosis with ruptured oesophageal varices as presenting manifestation of hereditary protein C deficiency. |
| title_full |
Portal vein thrombosis with ruptured oesophageal varices as presenting manifestation of hereditary protein C deficiency. |
| title_fullStr |
Portal vein thrombosis with ruptured oesophageal varices as presenting manifestation of hereditary protein C deficiency. |
| title_full_unstemmed |
Portal vein thrombosis with ruptured oesophageal varices as presenting manifestation of hereditary protein C deficiency. |
| title_sort |
portal vein thrombosis with ruptured oesophageal varices as presenting manifestation of hereditary protein c deficiency. |
| publishDate |
1988 |
| url |
https://ncbi.nlm.nih.gov/pmc/articles/PMC1433741/ https://ncbi.nlm.nih.gov/pubmed/3384371 |
| _version_ |
1760308224566755328 |