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Chordoma

Chordoma: Introduction

Chordoma: Chordomas are rare tumors that arise from embryonic notochordal remnants along the length of the neuraxis at developmentally active sites. These sites are the ends of the neuraxis and the vertebral bodies. More detailed information about the symptoms, causes, and treatments of Chordoma is available below.

Symptoms of Chordoma

Treatments for Chordoma

  • The treatment of chordomas depends on the extent and location of the tumor. In general, a more complete removal with wide excision delays the time interval between surgery and eventual recurrence
  • more treatments...»

Home Diagnostic Testing

Home medical testing related to Chordoma:

Wrongly Diagnosed with Chordoma?

Chordoma: Related Patient Stories

Chordoma: Complications

Read more about complications of Chordoma.

Causes of Chordoma

More information about causes of Chordoma:

Disease Topics Related To Chordoma

Research the causes of these diseases that are similar to, or related to, Chordoma:

Chordoma: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Chordoma

Spitz nevi misdiagnosed as dangerous melanoma skin cancer: One possible misdiagnosis to consider in lieu of melanoma is spitz nevi. See ...read more »

Chordoma: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Hospitals & Clinics: Chordoma

Research quality ratings and patient safety measures for medical facilities in specialties related to Chordoma:

Choosing the Best Hospital: More general information, not necessarily in relation to Chordoma, on hospital performance and surgical care quality:

Chordoma: Rare Types

Rare types of diseases and disorders in related medical categories:

Prognosis for Chordoma

Prognosis for Chordoma: The 5-year survival rate is estimated to be 51%, and the 10-year survival is estimated to be 35%.

Research about Chordoma

Visit our research pages for current research about Chordoma treatments.

Clinical Trials for Chordoma

The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.

Some of the clinical trials listed on ClinicalTrials.gov for Chordoma include:

Statistics for Chordoma

Chordoma: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Chordoma, or answer someone else's question, on our message boards:

Definitions of Chordoma:

A malignant bone tumor arising from remnants of the fetal notochord. Although it can occur at all ages, it is more frequently seen in middle-aged adults. Most frequent sites of involvement are: sacrococcygeal area, spheno-occipital area, and the cervico-thoraco-lumbar spine. Microscopically, chordomas are composed of cells that form cords and lobules, separated by mucoid intercellular tissue. Some of the cells are large (physaliphorous) and have vacuolated cytoplasm and prominent vesicular nuclei. Other tumor cells are small with small nuclei, without visible nucleoli. Chordomas tend to recur and may metastasize. The most common sites of metastasis are skin and bone. -- 2004 - (Source - Diseases Database)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Chordoma as a "rare disease".
Source - Orphanet

 

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