Malignant fibrous histiocytoma overview: Difference between revisions
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==Overview== | ==Overview== | ||
'''Malignant fibrous histiocytoma''' (MFH) is a type of [[cancer]] that is the most common [[Sarcoma|soft tissue sarcoma]] of late adult life, most commonly occurring between age 50-70. In rare cases MFH does occur in children, but it is usually in a less aggressive form. However, malignant tumors have occurred in children as young as 13. It occurs more often in caucasians than those of African or Asian descent. Its male:female predominance is 2:1. | '''Malignant fibrous histiocytoma''' (MFH) is a type of [[cancer]] that is the most common [[Sarcoma|soft tissue sarcoma]] of late adult life, most commonly occurring between age 50-70. In rare cases MFH does occur in children, but it is usually in a less aggressive form. However, malignant tumors have occurred in children as young as 13. It occurs more often in caucasians than those of African or Asian descent. Its male:female predominance is 2:1. | ||
==Treatment== | |||
Treatment consists of surgical removal (the extent of which ranges from tumor excision to limb amputation depending on the tumor) and in some cases [[chemotherapy]]. | |||
==References== | ==References== | ||
Revision as of 22:07, 22 January 2012
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Malignant fibrous histiocytoma Microchapters |
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Differentiating Malignant Fibrous Histiocytoma from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Malignant fibrous histiocytoma overview On the Web |
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American Roentgen Ray Society Images of Malignant fibrous histiocytoma overview |
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Directions to Hospitals Treating Malignant fibrous histiocytoma |
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Risk calculators and risk factors for Malignant fibrous histiocytoma overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Malignant fibrous histiocytoma (MFH) is a type of cancer that is the most common soft tissue sarcoma of late adult life, most commonly occurring between age 50-70. In rare cases MFH does occur in children, but it is usually in a less aggressive form. However, malignant tumors have occurred in children as young as 13. It occurs more often in caucasians than those of African or Asian descent. Its male:female predominance is 2:1.
Treatment
Treatment consists of surgical removal (the extent of which ranges from tumor excision to limb amputation depending on the tumor) and in some cases chemotherapy.