Hemangiopericytoma: A slow growing tumor that develops in deep soft tissues an tends to occur mainly in the abdomen (pelvic retroperitoneum specifically), hips, shoulders, upper arms and upper legs.
More detailed information about the symptoms,
causes, and treatments of Hemangiopericytoma is available below.
Symptoms of Hemangiopericytoma
See full list of 7
symptoms of Hemangiopericytoma
Home Diagnostic Testing
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Wrongly Diagnosed with Hemangiopericytoma?
Read more about complications of Hemangiopericytoma.
Causes of Hemangiopericytoma
Read more about causes of Hemangiopericytoma.
Disease Topics Related To Hemangiopericytoma
Research the causes of these diseases that are similar to, or related to, Hemangiopericytoma:
Less Common Symptoms of Hemangiopericytoma
Read more about symptoms of Hemangiopericytoma
Hemangiopericytoma: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and Hemangiopericytoma
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Read more about Misdiagnosis and Hemangiopericytoma
Hemangiopericytoma: Research Doctors & Specialists
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Hospitals & Clinics: Hemangiopericytoma
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on hospital performance and surgical care quality:
Hemangiopericytoma: Rare Types
Rare types of diseases and disorders in related medical categories:
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Prognosis for Hemangiopericytoma
Prognosis for Hemangiopericytoma:
only about a quarter of the tumors are malignant
More about prognosis of Hemangiopericytoma
Research about Hemangiopericytoma
Visit our research pages for current research about Hemangiopericytoma treatments.
Clinical Trials for Hemangiopericytoma
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 Hemangiopericytoma include:
See full list of 47
Clinical Trials for Hemangiopericytoma
Statistics for Hemangiopericytoma
Hemangiopericytoma: Broader Related Topics
Types of Hemangiopericytoma
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Definitions of Hemangiopericytoma:
A mesenchymal tumor of perivascular cell origin, composed of dilated vascular spaces (some with a staghorn or bifed shape) throughout the entire tumor. The tumor cells are surrounded by reticulin, are negative for muscle, nerve sheath, and epithelial markers, and are positive for CD34. The biologic behavior of hemangiopericytoma cannot always be predicted from the morphologic features. The 5- and 10-year survival rates of malignant hemangiopericytomas have been reported to be 40% and 29% respectively (partially adapted from S. Sternberg's Diagnostic Surgical Pathology, 3rd ed., 1999). -- 2004
- (Source - Diseases Database)
Hemangiopericytoma is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Hemangiopericytoma, or a subtype of Hemangiopericytoma,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Hemangiopericytoma as a "rare disease".
Source - Orphanet
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