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Radiologic-Pathologic Conference of Wilford Hall Medical Center |
1 Department of Radiology, Wilford Hall Medical Center, 2200 Bergquist Dr., Ste.
1, Lackland AFB, TX 78236-5300.
2 Department of Pathology, Wilford Hall Medical Center, San Antonio, TX
78236-5300.
3 Department of Radiology, Uniformed Services University of the Health Sciences,
4301 Jones Bridge Rd., Bethesda, MD 20814-4799.
Received September 23, 2002;
accepted after revision February 24, 2003.
Address correspondence to J. Q. Ly
(jly15544{at}hotmail.com).
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Aneurysmal bone cysts are benign expansile lesions that can be classified as primary (65%) or secondary (35%) [1]. Secondary aneurysmal bone cysts can arise from preexisting benign or malignant lesions. Most (80%) show the radiographic characteristics of the preexisting tumor. Many of these "blowout" lesions (as described by Jaffe [2]) destroy most of the underlying process, allowing a missed diagnosis of malignancy at histologic examination. To prevent misdiagnosis, it is essential that the radiologist report any atypical and malignant features. Common preexisting tumors include giant cell tumors, osteoblastomas, and angiomas [3]. Less common underlying processes include fibrous dysplasia, chondromyxoid fibroma, unicameral bone cyst, fibrous histiocytoma, eosinophilic granuloma, radiation osteitis, osteosarcoma, trauma, and fibrosarcoma [4]. The typical radiographic appearance of a primary aneurysmal bone cyst is an eccentric, expanded, and sometimes destructive osteolytic lesion that may contain internal septa. CT and MRI often show multiple fluid levels contained within thin-walled vascular cystic spaces. The fluid levels represent hemorrhage.
Chondroblastomas are rare tumors that occur predominantly in patients less than 20 years old. They occur almost exclusively in the epiphyses, but may extend into the diaphyses of long bones. They can be secondarily involved by an aneurysmal bone cyst in 1015% of cases [3]. Secondary involvement of a chondroblastoma by an aneurysmal bone cyst is more likely in patients older than 20 years. Early in the process, this phenomenon has the characteristics of solitary chondroblastoma: a patient less than 20 years old with a well-defined lytic epiphyseal lesion that shows geographic borders, punctate calcifications, chondroid matrix, periostitis, and bone marrow edema. The features of aneurysmal bone cyst appear later, with increasing destruction of the preexisting elements.
Intralesional fluidfluid levels are common to both chondroblastomas and aneurysmal bone cysts and are therefore not generally helpful for distinguishing the two entities. Histologic examination is required to make this determination. Histologically, a primary aneurysmal bone cyst shows blood-filled anastomosing fibrous-walled channels lined completely or incompletely by endothelial cells. The fibrous walls may contain hemosiderin deposits, giant cells, RBCs, and spicules of reactive bone [1]. The secondary aneurysmal bone cyst usually contains the additional characteristics of the coexisting lesion.
The treatment for aneurysmal bone cysts and chondroblastomascurettage and bone graftingis similar, which simplifies patient treatment.
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This article has been cited by other articles:
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H. J. Mankin, F. J. Hornicek, E. Ortiz-Cruz, J. Villafuerte, and M. C. Gebhardt Aneurysmal Bone Cyst: A Review of 150 Patients J. Clin. Oncol., September 20, 2005; 23(27): 6756 - 6762. [Abstract] [Full Text] [PDF] |
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