Hamartoma (patient information): Difference between revisions

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==Overview==
==Overview==
A hamartoma is defined as a focal growth that resembles a neoplasm but results from faulty development in an organ.They can occur anywhere in the body. They have been described in many organs but especially the chest, breast, skin and brain. They are also reported in the eye, colon and liver.


==What are the symptoms of Hamartoma?==
==What are the symptoms of Hamartoma?==
Symptoms depend upon the site of the lesion and they may present at any time from birth to middle age but usually early in life.


==What causes Hamartoma?==
==What causes Hamartoma?==


==Who is at highest risk?==
==Who is at highest risk?==
People with family history of hamartomatous syndrome, such as Cowden's disease,  tuberous sclerosis or Proteus' syndrome.


==Diagnosis==
==Diagnosis==
CXR, CT scan or MRI


==When to seek urgent medical care?==
==When to seek urgent medical care?==


==Treatment options==
==Treatment options==

Revision as of 23:28, 8 January 2016

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Hamartoma

Overview

What are the symptoms?

What are the causes?

Who is at highest risk?

Diagnosis

When to seek urgent medical care?

Treatment options

Where to find medical care for Hamartoma?

Prevention

What to expect (Outlook/Prognosis)?

Possible complications

Hamartoma On the Web

Ongoing Trials at Clinical Trials.gov

Images of Hamartoma

Videos on Hamartoma

FDA on Hamartoma

CDC on Hamartoma

Hamartoma in the news

Blogs on Hamartoma

Directions to Hospitals Treating Hamartoma

Risk calculators and risk factors for Hamartoma

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [2]

Overview

A hamartoma is defined as a focal growth that resembles a neoplasm but results from faulty development in an organ.They can occur anywhere in the body. They have been described in many organs but especially the chest, breast, skin and brain. They are also reported in the eye, colon and liver.

What are the symptoms of Hamartoma?

Symptoms depend upon the site of the lesion and they may present at any time from birth to middle age but usually early in life.

What causes Hamartoma?

Who is at highest risk?

People with family history of hamartomatous syndrome, such as Cowden's disease, tuberous sclerosis or Proteus' syndrome.

Diagnosis

CXR, CT scan or MRI

When to seek urgent medical care?

Treatment options

Where to find medical care for Hamartoma?

Directions to Hospitals Treating Hamartoma

Prevention of Hamartoma

What to expect (Outlook/Prognosis)?

Possible complications

Source

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