A case of Albright's syndrome (osteitis fibrosa disseminata)

Murray, R. C.; Kirkpatrick, H. J. R.; Forrai, Elemér

doi:10.1002/bjs.18003413308

Cited by 12 publications

(4 citation statements)

References 10 publications

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“…Any of the skeletal bones may show the disease, but it is commonest in the lower limbs, where the ilium, femur, and tibia are most often affected. Bowing of the extremities is well marked, as in patients reported by Braid (1932Braid ( , 1939 and by Murray et al (1946); and kyphosis and anterior bowing of the sternum have been described by Braid.…”

Section: The Bone Changesmentioning

confidence: 61%

Osteitis Fibrosa Disseminata

MacRae¹

1949

BMJ

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Section: The Bone Changesmentioning

confidence: 61%

Osteitis Fibrosa Disseminata

MacRae¹

1949

BMJ

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“…The author Lichtenstein [2], believes there is an abnormal enzymatic activity in the process of mesenchymal bone formation. But Murray [12], supports the hypothesis that there is a change in calcium and phosphorus metabolism. Attention to the occurrence of osteoblastic hyperplasia [13].…”

Section: Discussionmentioning

confidence: 83%

Craniofacial Fibrous Dysplasia Addressed Through The Intraoral And Nasal Access

Neto

Araujo²,

RamosSantana³

et al. 2015

Int Arch Med

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Background: The Craniofacial Fibrous Dysplasia is a benign disease, pseudoneoplasic, rare and asymptomatic of slow growth promoting replacement of bone tissue by an amorphous connective tissue, promoting bone deformation that can invade and cause compression of important structures such as the skull base and facial orbital bone. This study aims to present a clinical case of a Craniofacial Fibrous Dysplasia, emphasizing an alternative of an aesthetic surgical access by an intraoral approach.Case Report: We report the clinical case of patient IMS, 21 years of age with craniofacial fibrous dysplasia presenting deformity of the left facial middle third in orbital, nasal and maxilla region who was submitted to surgery for facial recontouring. The surgical access was intraoral associated with access for rhinoplasty. A lesion scrape was realized for facial recontouring and nasal osteotomy for correction of deviation caused by the injury. Conclusions: It was concluded that the surgical technique associatedwith the intraoral access with nasal extension is an important tool in addressing these lesions, allowing a large surgical field and satisfactory aesthetic and functional results without facial scars.

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“…The only abnormality of blood chemistry is the frequent elevation of the alkaline serum phosphatase. In the urine Bence-Jones protein was found in the patient of Murray, Kirkpatrick and Forrai (1946) and in one of Albright's patients.…”

Section: Discussionmentioning

confidence: 92%

Polyostotic Fibrous Dysplasia

Vines¹

1952

Archives of Disease in Childhood

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A case of Albright's syndrome (osteitis fibrosa disseminata)

Cited by 12 publications

References 10 publications

Osteitis Fibrosa Disseminata

Osteitis Fibrosa Disseminata

Craniofacial Fibrous Dysplasia Addressed Through The Intraoral And Nasal Access

Polyostotic Fibrous Dysplasia

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