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Sarcoma of heart
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Sarcoma of heart

This is a sarcomatous neoplasm resected from the heart. The arrow points to attached myocardial tissue.
The smooth and glistening lobulated asymetrical form is consistent with a malignant tumor. The histology is as variable as all soft tissue tumors, but angiosarcomas, rhabdomyosarcomas, and fibrosarcomas are most typical.
Sarcomas are difficult to cure surgically because of extensive grossly inapparent infiltration of adjoining tissues beyond widest possible margins of resection.
(Description By:J. Hasson, M.D. )
(Image Contrib. by: Hartford Hospital )
Sarcoma
Etiology

Unknown.
Pathogenesis

Unknown,
Epidemiology

Angiosarcomas are the most common type. However, any type of soft tissue sarcomas can occur in the heart.
These are all rare tumors.
General Gross Description

The angiosarcomas typically involve the right side, usually the right atrium.
Any anatomic site is subject to involvement within the heart, with extension in any direction, and possibly involving the parietal pericardium as well.
General Microscopic Description

Varies according to which of the soft tissue tumors is identified.
Some examples are too undifferentiated to classify, even with advances in immunohistochemistry.
Clinical Correlation

Clinical presentation may be due to any combination of one or more of the following 3 pathophysiological mechanisms: 1. Arrhythmias 2. Mechanical obstructive effects, e.g. obstruction of any valve with right or left sided heart failure. Mitral and pulmonic valves most commonly involved. 3. Systemic "acute phase reactions", fever, weight loss, and malaise (TNF?, interleukin-6?), even before cardiac manifestations appear.
Survival for at most one year after symptoms ensue.
Aggressive surgery is appropriate with successes and failures.
References

Cardiovascular Pathology, 2nd ed. Silver MD (ed), Philadelphia: Saunders, 1991. pp. 1324-1331.
Sarcoma
Synopsis by: J. Hasson, MD (T32100M89003)[359]
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