Carotid artery protection with levator scapulae muscle.
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This report presents the interesting case of a 50-year-old white man with an unusual benign tumor composed predominantly of a proliferation of atypical endothelial cells combined with a variable inflammatory response. This case represents an instance of the recently renamed entity "histiocytoid hemangioma" in which two organ systems are involved. Both skin and bone showed typical lesions. No physical connection jointed the separate lesions. The results of examination by light microscopy, electron microscopy, and immunoperoxidase examination for lysozyme and Factor VIII are reported. The significance of this case is that it supports the concept of classifying similar vascular lesions, despite varied organ system origin, into a single entity, the histiocytoid hemangioma.
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We describe a patient with the rare autosomal dominant syndrome of congenital glenoid dysplasia. The severity of the findings resulted in an intense and effective radiological and clinical work-up including MRI, CT reconstruction, and fluoroscopy.
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We have presented an unusual case of chondroblastoma mimicking a malignant tumor. Retrospective review of radiographs obtained 19 years before the diagnosis gave us a unique opportunity to follow the natural history of this atypical lesion.
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A case of metastatic pheochromocytoma of the reconstruction of the shoulder joint is reported. During the operation elevation of the blood pressure was controlled by venous injection of alpha-blocker and ligation of the three main feeder arteries and veins.
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