Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-t5tsf Total loading time: 0 Render date: 2024-11-02T21:55:23.652Z Has data issue: false hasContentIssue false

12 - LEIOMYOMAS

Published online by Cambridge University Press:  23 December 2009

Camran Nezhat
Affiliation:
Stanford University School of Medicine, California
Farr Nezhat
Affiliation:
Mount Sinai School of Medicine, New York
Ceana Nezhat
Affiliation:
Nezhat Medical Center, Atlanta
Get access

Summary

As more articles debating the prevalence of hysterectomies appear in the lay press and on the Internet, increasing numbers of women are demanding alternative procedures. A recent New York Times article decrying the prevalence of hysterectomies stated that by the age of 60, one in three women in the United States will have had her uterus removed. By comparison, in Italy the figure is one in six, whereas in France, it is one in 18 women. Of the 600,000 hysterectomies performed annually in the United States, one third are done for leiomyomas. This number rises dramatically for women over the age of 40 and for those in certain ethnic groups. For African American women, 61.3% of hysterectomies are done for leiomyomas, and for women in the 45-to-54—year age group, 53% of all hysterectomies, regardless of race, are done for this indication. It is estimated that more than 25% of women over the age of 36 have one or more leiomyomas, with 50% of these being symptomatic.

Uterine leiomyomas (myomas) are benign smooth muscle tumors arising from the myometrium. Despite the fact that myomas are quite common, very little is known about their etiology. They are monoclonal — arising from a single myometrial cell. Different karyotypes of multiple myomas have been found in the same patient.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2008

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
×