نتایج جستجو برای: polyostotic

تعداد نتایج: 334  

Journal: :AJR. American journal of roentgenology 2002
Vincent F H Chong James B K Khoo Yoke-Fun Fan

717 ibrous dysplasia is a developmental anomaly that can affect any bone in the body. The skull and facial bones are the affected sites in 10–25% of patients with monostotic fibrous dysplasia and in 50% of patients with polyostotic fibrous dysplasia. Conventional radiographic findings reveal characteristics of fibrous dysplasia. CT findings also show characteristics of fibrous dysplasia and con...

2017
Eliana Dantas da COSTA Priscila Dias PEYNEAU Francielle Silvestre VERNER Solange Maria de ALMEIDA Glaucia Maria Bovi AMBROSANO

Fibrous dysplasia is a benign fibrous-osseous lesion in which normal bone is replaced by fibrous connective tissue and immature bone, affecting only one (monostotic) or several bones (polyostotic) and mainly occurring in children and young adults. When present in facial bones, the maxilla is more frequently involved than the mandible, which can cause facial asymmetry in addition to dental compl...

Journal: :The Journal of the Association of Physicians of India 2006
K Bhatt C Balakrishnan G Mangat K Bajan T Ashavaid V R Joshi

Paget's disease is uncommon in Asians. We present 3 patients with varying manifestations. A 50 years old lady was detected to have raised alkaline phosphatase at a routine health check-up. Isoenzyme studies confirmed its bony origin. Bone scan revealed polyostotic disease. A 65 years old male patient with known Paget's disease of 6 years duration presented with pelvic girdle pain, progressive i...

2013
Surojit Mondal Aniket Chowdhury Goutam Bandyopadhyay

Fibrous Dysplasia of bone is an uncommon congenital skeletal disorder that is found equally in both genders and is not inherited. Fibrous Dysplasia is characterized either monostotic or polyostotic, and may occur as a component of McCune Albright Syndrome or the rare Mazabraud Syndrome. Long bones, skull bones and ribs are most commonly affected bones. We present a case of a 18 years old boy ha...

2011
Paola Dal Cin

It is characterized by a broad clinical spectrum, varying from the more frequent solitary (monostatic) asymptomatic lesion to extensive and severe multifocal (polyostatic) lesions. The monostotic variant most commonly affects the ribs, femur and tibia of older children and young adults. The less frequent polyostotic type may be associated with endocrine abnormalities, skin hyperpigmentation and...

2016
Jura Numminen Markus Rautiainen

Fibrous dysplasia; Nasal cavity; Skull base; Endoscopic sinus surgery Abstract Fibrous dysplasia is an uncommon benign tumour in the nasal cavity. Due to adjacent vital soft tissue structures surgery is often the treatment of choice. We report a rare case of polyostotic fibrous dysplasia of the mandible and the ethmoid bone including nasal bony septum with intracranial expansion, and include a ...

2012
D. Bahar Genç M. Alp Özkan Atilla Büyükgebiz

Fibrous dysplasia (FD) is categorized as either monostotic or polyostotic and may occur as a component of McCune-Albright syndrome (MAS). Imaging findings can mimic neoplastic diseases. We present a case of MAS initially suspected to have neoplastic disease. A 9-year-old girl was admitted to pediatric emergency with ataxia. Upon hospitalization, an extradural mass was seen on cranial magnetic r...

2012
Robert P Stanton Ernesto Ippolito Dempsey Springfield Lynn Lindaman Shlomo Wientroub Arabella Leet

The surgical management of Polyostotic Fibrous Dysplasia (FD) of bone is technically demanding. The most effective methods to manage the associated bone deformity remain unclear. The marked variation in the degree and pattern of bone involvement has made it difficult to acquire data to guide the surgeon's approach to these patients. In light of the paucity of data, but need for guidance, recogn...

2011
E Atsali KD Stathopoulos E Stefos H Bournazos G Kiniklis A Papadimitriou P Nicolaidou AB Zoubos G Skarantavos

Methods We present a 14y old girl with polyostotic fibrous dysplasia (right humerus, femur, tibia, skull), precocious puberty and café au lait skin spots, diagnosed as MAS with a confirmed heterozygous c.601C>T mutation of the GNAS1 gene. Due to initial bone pain and continuously increasing bone turnover, the patient was treated with iv bisphosphonates for 4 years. We used pQCT to estimate bone...

Journal: :Archives of Iranian medicine 2010
Sepideh Siadati Ensiyeh Shafigh

Fibrous dysplasia is a benign bone lesion of unknown etiology. Bone involvement usually is solitary (monostotic). Multiple forms (polyostotic) associated with extra skeletal symptoms, particularly cutaneous pigmentation, endocrine dysfunction and precocious puberty is called McCune-Albright syndrome (MAS). We report the case of a 40-year-old man who presented with left mandibular body expansion...

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