Malignant fibrous histiocytoma associated with a bone infarct in a patient with hereditary bone dysplasia

被引：0
|
作者：
S. Kenan
Ibrahim Fikry Abdelwahab
George Hermann
Michael J. Klein
机构：
[1] Hospital for Joint Diseases,
[2] Orthopedic Institute,undefined
[3] 301 East 17th Street,undefined
[4] New York,undefined
[5] N.Y. 10003,undefined
[6] USA,undefined
[7] Department of Radiology,undefined
[8] The Mount Sinai School of Medicine,undefined
[9] New York,undefined
[10] New York,undefined
[11] USA,undefined
[12] Department of Pathology,undefined
[13] The Mount Sinai School of Medicine,undefined
[14] New York,undefined
[15] New York,undefined
[16] USA,undefined
来源：
Skeletal Radiology | 1998年 / 27卷
关键词：
Key words Bone infarct; Malignant fibrous histiocytoma; Hereditary bone dysplasia;
D O I：
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学科分类号：
摘要：
Hereditary bone dysplasia (HBD) is an extremely rare clinicopathological entity manifested by diaphyseal medullary stenosis and cortical bone thickening associated with a propensity for fractures affecting the long tubular bone. Malignant transformation has been reported to occur at an alarming frequency. The hereditary pattern appears to be autosomal dominant. In this paper we present the case of a 19-year-old man with hereditary bone dysplasia who was unaware of his underlying condition until he presented with malignant transformation arising in an area of bone infarct of the left tibia.
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页码：463 / 467
页数：4
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