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Painless urethral bleeding: an unusual presentation of Von Willebrand disease.
Armenian, S; Raffel, J L; Nugent, D J; Young, G.
Afiliação
  • Armenian S; Division of Hematology, Children's Hospital of Orange County, Orange, CA 92868, USA.
Haemophilia ; 9(3): 332-5, 2003 May.
Article em En | MEDLINE | ID: mdl-12694526
ABSTRACT
Von Willebrand disease (vWD) is the most common bleeding disorder, and usually presents with either easy bruising or mucus membrane bleeding. Many patients are also diagnosed as a result of abnormal pre-operative laboratory tests. In this report, we describe two patients presenting with painless, persistent urethral bleeding as their initial manifestation of vWD. The first patient began bleeding after a Foley catheter was placed during a hospital admission for status epilepticus. A urologic examination demonstrated a wound in the posterior urethra. Despite repeated attempts at controlling the bleeding with cautery, the bleeding persisted. The second patient presented with spontaneous urethral bleeding and a normal urologic examination. Due to persistent bleeding, both patients underwent a coagulation evaluation that demonstrated the presence of type 1 vWD. The first patient had resolution of his bleeding following 5 weeks of Alphanate, a von Willebrand factor containing factor VIII concentrate, and aminocaproic acid. The second patient initially responded to desmopressin, but subsequently required Humate-P to achieve complete resolution. These cases illustrate the importance of an evaluation for bleeding disorders in patients with persistent bleeding from any site.
Assuntos
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Base de dados: MEDLINE Assunto principal: Doenças Uretrais / Doenças de von Willebrand / Hemorragia Idioma: En Ano de publicação: 2003 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Doenças Uretrais / Doenças de von Willebrand / Hemorragia Idioma: En Ano de publicação: 2003 Tipo de documento: Article