Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-mlc7c Total loading time: 0 Render date: 2024-11-20T00:25:38.800Z Has data issue: false hasContentIssue false

6 - Gynaecological problems in women with bleeding disorders

Published online by Cambridge University Press:  05 October 2014

Rezan Abdul-Kadir
Affiliation:
Royal Free Hospital
Christine Lee
Affiliation:
Royal Free Hospital
Ann Harper
Affiliation:
Royal Jubilee Maternity Belfast
Get access

Summary

Excessive or abnormal vaginal bleeding are the most common symptoms when women present to a gynaecologist. The cause is usually gynaecological pathology but occasionally gynaecologists may encounter women with such symptoms secondary to inherited or acquired bleeding disorders. This chapter aims to increase awareness and provide basic information about these relatively uncommon disorders. Gynaecological complications associated with these disorders and their management will also be discussed.

Inherited bleeding disorders

VON WILLEBRAND'S DISORDER

Inherited bleeding disorders in women are far more common than previously suspected. Von Willebrand's disorder seems to be the most common inherited haemorrhagic disorder in women, with an estimated prevalence of 1–3%. Von Willebrand's disorder is a consequence of quantitative and/or qualitative defects of von Willebrand factor (VWF), a protein that is necessary for platelet adhesion and thrombus formation and which also serves as a carrier for factor FVIII.

Von Willebrand's disorder demonstrates extreme clinical and genetic heterogeneity depending on the subtype considered. There are three main types: types 1 and 3 caused by quantitative and type 2 caused by qualitative defects in VWF protein.

• Type 1 (70% of all cases) is the most common form of the disease. It is characterised by low plasma levels, usually between 5 iu/dl and 40 iu/dl, of FVIII (normal range 50–150 iu/dl) and VWF (normal range 50–175 iu/dl). This is caused by reduced production of normally functioning VWF, resulting in a secondary defect of FVIII.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2005

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×