A Case of Heyde's Syndrome with Abnormal von Willebrand Factor / 대한소화기학회지
The Korean Journal of Gastroenterology
;
: 133-136, 2004.
Artículo
en Coreano
| WPRIM
| ID: wpr-11993
ABSTRACT
A 68-year-old woman with known severe aortic stenosis was admitted to the hospital because of hematochezia and dizziness. She had received several blood transfusions over the preceding 3 years and undergone right hemicolectomy 2 years ago for severe lower gastrointestinal bleeding. Postoperative histology revealed angiodysplasia involving the ascending colon. After the hemicolectomy, she continued to have hematochezia and anemia and required additional blood transfusions for anemia. During this admission, platelet count, activated partial-thromboplastin time, von Willebrand factor antigen, and von Willebrand factor ristocetin cofactor were normal. She had a severe deficiency of high-molecular-weight multimers of von Willebrand factor. Colonoscopy showed angiodysplasia in the transverse colon at this time. Successful coagulation of the bleeding angiodysplasia was achieved by argon plasma coagulator. No additional bleeding was observed thereafter. We report a case of Heyde's syndrome with abnormal von Willebrand factor in a patient who presented with intestinal angiodysplasia and aortic stenosis.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Estenosis de la Válvula Aórtica
/
Síndrome
/
Enfermedades de von Willebrand
/
Resumen en Inglés
/
Angiodisplasia
/
Enfermedades del Colon
/
Hemorragia Gastrointestinal
/
Anemia
Límite:
Anciano
/
Femenino
/
Humanos
Idioma:
Coreano
Revista:
The Korean Journal of Gastroenterology
Año:
2004
Tipo del documento:
Artículo
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