نتایج جستجو برای: fibrous dysplasia of bone

تعداد نتایج: 21202898  

2010
S Mallina

Med J Malaysia Vol 62 No 2 June 2007 SUMMARY Fibrous dysplasia is a benign disease characterized by a progressive replacement of normal bone elements with fibrous tissue and the temporal bone involvement is uncommon. It has a male:female ratio of 2:1 and is seen more commonly in the first two decades of life. Diagnosis is made based on radiological findings and the modality of treatment is main...

Journal: :Acta pathologica, microbiologica, et immunologica Scandinavica. Section A, Pathology 1983
L Sundkvist

Thanatophoric dysplasia is an osteochondrodysplasia always lethal already in the neonatal period. Three cases, showing the characteristic X-ray picture of the disease, are described. Histopathologically, an abnormality in the endochondral ossification process was observed. In sections from tubular bones the growth zone was found to be irregular with deficient chondrocyte maturation, absence of ...

Journal: :Sarcoma 2003
C. L. M. H. Gibbons M. Petra R. Smith N. A. Athanasou

Growth of benign tumours and tumour-like lesions of bone results in osteolysis which may cause pathological fracture. Bisphosphonates are anti-osteolytic agents which have proved effective in the treatment of number of osteolytic conditions. In this study we report the results of treatment with the aminobisphosphonate, pamidronate, of three benign osteolytic tumours of bone, two cases of fibrou...

Journal: :Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale 2004
R Saetti M Silvestrini F Marino S Narne

Fibrous dysplasia, a rare bony disease, is characterised by substitution of normal bone with immature tissue embedded in a fibrous stroma. It can be either monostotic or involve several bones. Fibrous dysplasia is usually asymptomatic but, in the advanced stage, pain due to neural compression or pathological fractures may occur. In the case of cranio-facial involvement, ocular, masticatory, res...

2009
Ping Li Zai-Ren Zhang Ying Jiang Xu-Dong Xia Dan Wang Xian-Feng Li

INTRODUCTION McCune-Albright syndrome (MAS) is a rare disorder characterized by the classic triad of precocious puberty, polyostotic fibrous dysplasia and café-au-lait pigmented skin lesions. Cystic change is rare in fibrous dysplasia (FD), especially in McCune-Albright syndrome. There were no reports about cyst degeneration in MAS which resulted in abnormal visual acuity and visual fields. Her...

Journal: :Endocrine journal 2006
Haluk Sargin Hulya Gozu Rifat Bircan Mehmet Sargin Melike Avsar Gazenfer Ekinci Ali Yayla Ilker Gulec Mustafa Bozbuga Beyazit Cirakoglu Refik Tanakol

The syndrome of McCune-Albright syndrome (MAS) is clasically defined as a triad presentation with the findings of polyostotic fibrous dysplasia, café-au-lait spots, and sexual precocity. However, not all patients present with complete symptoms. A 52-year-old man was diagnosed as having a variant of McCune-Albright syndrome with the following findings: polyostotic fibrous dysplasia, acromegaly d...

Journal: :Nihon Bika Gakkai Kaishi (Japanese Journal of Rhinology) 2019

Journal: :Journal of College of Medical Sciences-nepal 2022

Fibrous dysplasia is a rare bone condition in which normal replaced by aberrant fibrous tissue. The patient may come to evaluate with other diseases and while doing investigations, it observed. Here we present case of 24 years male who came our OPD swelling around the left cheek region for 5 days. underwent Computerised tomography scan revealed an expansile, sclerotic, cystic ground-glass appea...

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