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Latest revision as of 14:50, 18 August 2015

Chordoma Microchapters

Home

Patient Information

Overview

Historical Perspective

Pathophysiology

Epidemiology and Demographics

Risk Factors

Screening

Causes

Differentiating Chordoma from other Diseases

Natural History, Complications and Prognosis

Diagnosis

Staging

History and Symptoms

Physical Examination

Laboratory Findings

Chest X Ray

CT

MRI

Echocardiography or Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Chordoma classification On the Web

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US National Guidelines Clearinghouse

NICE Guidance

FDA on Chordoma classification

CDC on Chordoma classification

Chordoma classification in the news

Blogs on Chordoma classification

Directions to Hospitals Treating Chordoma

Risk calculators and risk factors for Chordoma classification

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

There are three histological variants of chordoma: classical, chondroid and dedifferentiated. The histological appearance of classical chordoma is of a lobulated tumor composed of groups of cells separated by fibrous septa. The cells have small round nuclei and abundant vacuolated cytoplasm, sometimes described as physaliferous (resembling a spider's web). Chondroid chordomas histologically show features of both chordoma and chondrosarcoma.

References


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