Embryonal carcinoma differential diagnosis: Difference between revisions

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[[Category:Types of cancer]]
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[[Category:Endocrinology]]
[[Category:Endocrinology]]
[[Category:Oncology]]
[[Category:Gynecology]]
[[Category:Gynecology]]
[[Category:Pediatrics]]
[[Category:Pediatrics]]

Latest revision as of 15:07, 20 August 2015

Embryonal carcinoma Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Epidemiology and Demographics

Risk Factors

Differentiating Embryonal carcinoma from other Diseases

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Staging

Laboratory Findings

CT

MRI

Ultrasound

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Other Diagnostic Studies

Treatment

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Primary Prevention

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Case #1

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

Overview

Risk Factors

Differing from the other types of testicular cancers, the embryonal carcinoma can have several of the properties of a mal-developed fetus, including cartilage. The main tumor is, on average, 2.5 centimeters long and can also stem out approximately 9 centimeters up the testicular cord. Embryonal carcinomas are usually seen in males age 25-35, but have also hit males as young as their late teens. The chances of an embryonal carcinoma spreading from one testicle to the other are less than 1%. Embryonal carcinomas account for approximately 40% of testicular tumors.

Rarely, embryonal carcinomas are seen in females, in the ovaries.

References


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