Please note: In order to keep Hive up to date and provide users with the best features, we are no longer able to fully support Internet Explorer. The site is still available to you, however some sections of the site may appear broken. We would encourage you to move to a more modern browser like Firefox, Edge or Chrome in order to experience the site fully.

Leiomyosarcoma : Risk Factors, Diagnosis and Treatment Options, PDF eBook

Leiomyosarcoma : Risk Factors, Diagnosis and Treatment Options PDF

Edited by Rosemary H Leach

PDF

Please note: eBooks can only be purchased with a UK issued credit card and all our eBooks (ePub and PDF) are DRM protected.

Description

Leiomyosarcomas (LMS) are soft tissue tumors derived from smooth muscles cells, often in the uterus, retroperitoneum, skin, vessels, and bone.

They are one of the most common types of sarcoma. Most leiomyosarcomas are sporadic, but may develop in the setting of genetic syndomes such as hereditary retinoblastoma and L-Fraumeni syndrome. Leiomyosarcomas may also be a result of radiation exposure; however, radiation-induced sarcomas are typically undifferentiated, fibrosarcomas or malignant peripheral nerve sheath tumors.

Like other sarcomas, prognosis is worse with higher grade tumors.

Although chemotherapy and radiation are sometimes used as adjuvant therapy, the mainstay of therapy, and the only chance for cure, is surgery.

The management of LMS is especially complex when the tumor involves major blood vessels.

This book discusses the diagnosis and treatments most effectively used for Leiomyosarcomas.

It also provides insight on the specific areas that LMS is found and how it affects that area.

Information

Information