Case report of hereditary hemorrhagic telangiectasia with severe anemia
نویسندگان
چکیده
منابع مشابه
Hereditary hemorrhagic telangiectasia: a rare cause of severe anemia.
Hereditary hemorrhagic telangiectasia is an autosomal dominant disease in which arteriovenous communications are typically seen in the skin, mucosal surfaces, lungs, brain and gastrointestinal tract. This disease typically presents as epistaxis, gastrointestinal bleeding and arteriovenous malformations (in the brain and lungs). Although the epistaxis and gastrointestinal bleeding can result in ...
متن کاملWoman presenting with chronic iron deficiency anemia associated with hereditary hemorrhagic telangiectasia: a case report
BACKGROUND Hereditary hemorrhagic telangiectasia is an autosomal dominant disorder associated with frequent nose bleeds that can be troublesome and difficult to contain. A further manifestation is telangiectasia, which may develop in the upper and lower gastrointestinal tract. The associated blood loss can be chronic, resulting in iron deficiency anemia which, when severe, has historically been...
متن کاملHereditary Hemorrhagic Telangiectasia: Presenting with Epistaxis. A Case Report
1 Assistant Professor, Department of Cardiac Anaesthesiology Institute of Postgraduate Medical Education & Research, Kolkata, India 2 Assistant Professor, Department of Anaesthesiology, Kishanganj Medical College, Kolkata, India 3 PDT Department of Cardiac Anaesthesiology Institute of Postgraduate Medical Education & Research, Kolkata 4 Professor Department of Anaesthesiology, N.R.S Medical Col...
متن کاملA case of hereditary hemorrhagic telangiectasia.
Hereditary hemorrhagic telangiectasia, also known as Osler-Weber-Rendu disease, is an autosomal dominant disorder of the fibrovascular tissue. It is characterized by the classic triad of mucocutaneous telangiectasias, recurrent hemorrhages, and familial occurrence. The cutaneous manifestation appear clinically as punctuate, linear, or splinter-like telangiectasias of the upper body, oral, and n...
متن کاملCASE REPORT Pregnancy With Uterine Vascular Malformations Associated With Hemorrhagic Hereditary Telangiectasia: A Case Report
Background: Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant condition. It is rarely seen in pregnancy and even more rarely has uterine manifestations. Case: A 29-year-old primigravid woman with HHT was noted to have vascular manifestations of her disease in the lower uterus, distal rectum, pelvis, and bladder before pregnancy. Prior to delivery, a case conference was he...
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ژورنال
عنوان ژورنال: Biochemia Medica
سال: 2008
ISSN: 1846-7482
DOI: 10.11613/bm.2008.012