نتایج جستجو برای: polyostotic

تعداد نتایج: 334  

Journal: :Clinical proceedings - Children's Hospital of the District of Columbia 1946
J HOULI F P DE CASTRO E AMORIM S KAISER G D VELOSO

Journal: :Nuclear medicine review. Central & Eastern Europe 2004
Daniela Chroustova Michal Votruba Jan Sprindrich Bohuslav Sosna

The case of a 12-year-old girl with Jaffé-Lichtenstein-Uehlinger syndrome is presented. A bone scan pattern exhibits clinical symptoms, X ray images and histological findings are described in a case of polyostotic form of the fibrous dysplasia. A biopsy with histology was performed in consideration of bone scan findings and a confirmed final diagnosis.

Journal: :The Journal of bone and joint surgery. British volume 1986
R L Diercks A J Sauter W M Mallens

A patient with polyostotic fibrous dysplasia had several fractures of the right lower limb. An above-knee amputation was eventually performed, followed by arthrodesis of the hip. Five years later the stump became painful and swelled with dramatic rapidity. Biopsy showed that this was not due to malignant change, but that an aneurysmal bone cyst had developed in association with the fibrous dysp...

Journal: :Acta orthopaedica Belgica 2007
Loek Verlaan Bart van der Wal Geert-Jan de Maat Geert Walenkamp Lizette Nollen-Lopez André van Ooij

Primary hyperparathyroidism is due most often to a parathyroid adenoma secreting parathyroid hormone. Elevated PTH levels cause bone resorption, the formation of polyostotic lesions and a reduction in bone mineral density, predisposing to pathological fractures. The final stage of this disease is osteitis fibrosa cystica. The authors review the literature about osteitis fibrosa cystica and the ...

Journal: :Reumatologia clinica 2014
Carlos Francisco Meneses Antonio Egües Miren Uriarte Joaquín Belzunegui

A 37-year-old woman with a fibrous polyostotic dysplasia (FPD) of the left femur, tibia and foot was diagnosed at 11 years of age. At the onset she presented mechanical pain of the left hip and later a stress fracture of the femur for which she was treated with surgery, pamidronate and zolendronate. Pathology confirmed the diagnosis. Phosphocalcic metabolism was normal. X-rays (Fig. 1) showeda ...

2016
Yadan Fan Jiannan Liu Chenping Zhang Zhiyuan Zhang Huawei Yang Jingzhou Hu

Objective: To analyse the clinical characteristics and imaging findings of maxillofacial fibrous dysplasia and the relationship between serum alkaline phosphatase and its clinical relative factors. Method: The clinical materials of 72 fibrous dysplasia patients were reviewed and the alkaline phosphatase among monostotic fibrous dysplasia, polyostotic fibrous dysplasia and non-fibrous dysplasia ...

Journal: :The Journal of bone and joint surgery. American volume 2004
Arabella I Leet Edward Magur Janice S Lee Shlomo Wientroub Pamela G Robey Michael T Collins

BACKGROUND Lesions of fibrous dysplasia involving the spine and scoliosis are thought to be uncommon entities in patients with polyostotic fibrous dysplasia and McCune-Albright syndrome. By examining bone scans of a relatively large cohort of patients with these disorders, we sought to determine the prevalence of spinal involvement and any association with scoliosis. METHODS Sixty-two patient...

Journal: :journal of dentomaxillofacil radiology, pathology and surgery 0
elahe mahmoudi hashemi department of oral and maxillofacial radiology, north khorasan university of medical sciences, dental school, bojnurd, iran mahrokh imanimoghaddam department of oral and maxillofacial radiology, mashhad university of medical sciences, dental school, mashhad, iran somayeh nemati department of oral and maxillofacial radiology, guilan university of medical sciences, dental school, rasht, iran zohre dalir department of oral medicine, mashhad university of medical sciences, dental school, mashhad, iran

fibrous dysplasia (fd) is an osseous growth dis-order, producing immature bone and characte-rized by the replacement of normal bone with fibro-osseous connective tissue. it is a bone dys-plasia that has the potential to cause significant cosmetic and functional disturbances, particularly in the craniofacial skeleton. cra-niofacial fibrous dysplasia is one of the three types of polyostotic fibro...

Journal: :international journal of pediatrics 0
moein mobini department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran. rahim vakili department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran. saba vakili department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran.

mccune-albright syndrome (mas) is a rare, heterogenous, clinical condition caused by a rare genetic mutation. the disorder is more common in females and is characterized by a triad of cutaneous, bone and endocrine abnormalities.  we describe a girl patient with mas having precocious puberty and multiple cafe-au-lait macules and deforming polyostotic fibrous dysplasia of bone. clinical presentat...

Journal: :Global Journal of Orthopedics Research 2020

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