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fibrous dysplasia of bone/nàusea

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Different clinical presentation and management of temporal bone fibrous dysplasia in children.

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BACKGROUND Fibrous dysplasia is a slowly progressive benign fibro-osseous disorder that involves one or multiple bones with a unilateral distribution in most cases. It is a lesion of unknown etiology, uncertain pathogenesis, and diverse histopathology. Temporal bone involvement is the least

Osteoblastoma of the frontal bone invading the orbital roof: A case report.

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BACKGROUND Osteoblastoma is an uncommon primary bone tumor that involves any part of the skeleton. But its occurrence in the skull is extremely rare. UNASSIGNED A 30-year-old female was admitted to our hospital, because of the mass in the right frontal region with the history of headache for 3 years
The use of octreotide-LAR and cabergoline therapy has shown great promise in adults with acromegaly; however, the experience in pediatric patients has rarely been reported. We described a clinical course of a 15-year-old boy of McCune-Albright syndrome (MAS) with pituitary gigantism. At the age of 8

A case of Albright's syndrome treated with calcitonin.

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A 23-year-old woman with Albright's syndrome (polyostotic fibrous dysplasia of bone, precocious puberty and irregular cutaneous pigmentations) had sustained multiple fractures and was grossly disabled. Evaluation disclosed markedly raised serum alkaline phosphatases and a high urinary excretion of
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