Thrombophlebitis migrans including Mondors’ syndrome and autoimmune hemolytic anemia in ulcerative colitis; case report and review of the literature

 
This item is provided by the institution :

Repository :
Annals of Gastroenterology
see the original item page
in the repository's web site and access all digital files if the item*
share




2007 (EN)

Thrombophlebitis migrans including Mondors’ syndrome and autoimmune hemolytic anemia in ulcerative colitis; case report and review of the literature (EN)

Margarita Kitsanou, G. Kalambokis,Svetlana Leonidi, E.V. Tsianos, K.H. Katsanos, D.K. Christodoulou,

SUMMARY Thromboembolic events occur in UC and Crohn’s disease. Activation of clotting factors and thrombocytosis are common. In ulcerative colitis, increased levels of factor V, factor VIII and fibrinogen and decreased levels of antithrombin III have been demonstrated. Deep vein thrombosis and pulmonary emboli affect patients with severe disease and may occur after colectomy. Thromboembolic events in the eye or intracranial vessels have been described. Coombs positive hemolytic anemia has occasionally been reported in patients with ulcerative colitis. In some of these rare cases, hemolytic anemia was the main problem of the patient and was cured by colectomy. A case of a young female patient with ulcerative colitis, autoimmune hemolytic anemia, recurrent deep vein thromboses including Mondors’ syndrome and menstrual abnormalities is reported. There are several convincing reports that associate UC with Coombs positive hemolytic anemia and this co-existence should be considered in every UC patient with persisting or severe anemia. Before relating autoimmune anemia to UC, other causes of hemolysis should be excluded.The treatment of persistent autoimmune hemolytic anemia in UC patients could probably include administration of cyclosporine as there is a report of improvement of anemia after weeks of treatment. Methotrexate or azathioprine are alternative agents. Anti-influenza vaccination should invariably be performed in all IBD patients treated with immunosuppressive agents. Steroids should not be withdrawn or administered at reduced doses in cases of severe autoimmune hemolytic anemia.Patients with hypercoagulable states, thrombotic events and IBD usually require careful administration of anticoagulant agents. Sulfasalazine or azathioprine may reduce the effect of oral coumarin anticoagulants, while heparin is usually effective. Low molecular weight heparin may be used as a chronic regimen if required, balancing the dose at safe levels. (EN)

info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion


English

2007-03-19


Hellenic Society of Gastroenterology (EN)

1792-7463
1108-7471
Annals of Gastroenterology; Volume 15, No 2 (2002) (EN)




*Institutions are responsible for keeping their URLs functional (digital file, item page in repository site)