نتایج جستجو برای: rib exostosis

تعداد نتایج: 11577  

Journal: :Proceedings of the Royal Society of Medicine 1920

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ژورنال: مجله علمی دانشگاه علوم پزشکی بیرجند 2013
مرتضوی مقدم, غلامرضا,

Primary hyperparathyroidism is a benign disease and is most often diagnosed during routine calcium measurement. It would be astonishing if a patient is symptomatic, but the diagnosis is neglected. A 56-year-old woman was admitted with complaint of localized pain in the chest wall following a regular bending and straightening. CXR showed a mass like lesion of the chest wall on the left and also ...

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2016
Alessandro Villa Domenico Gerardo Iacopino Francesca Graziano Carlo Gulì Antonella Giugno Luigi Basile Rosario Maugeri

Osteochondroma, also known as osteocartilaginous exostosis or just exostosis, was initially described in 1843 by Reid [1]; it is a common benign tumor of the bone accounting for 10% to 15% of all bone tumors and 20% to 50% of all benign bone tumors [2]. These lesions are the most common benign tumors of the appendicular skeleton, located in the metaphyseal region of long bones, particularly the...

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2018
Georgi Tchernev Yavor Grigorov Stanislav Philipov Anastasiya Chokoeva Uwe Wollina Torello Lotti Jose Cardoso Irina Yungareva Ilia Lozev Georgi Konstantinov Maximov

BACKGROUND Subungual exostosis is a relatively uncommon, benign osteocartilaginous tumor of the distal phalanx of the toes or fingers in young adults, considered as a rare variant of osteochondroma. Differential diagnoses include subungual verruca (viral wart), pyogenic granuloma, osteochondroma, amelanotic subungual melanoma and glomus tumour. Misdiagnosis and total onychodystrophy frequently ...

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Journal: :acta medica iranica 0
z moinfar f. davari tanha z. moinfar m. kaveh s. eftekhari s. eftekhari z. khalilpour

short rib polydactyly syndrome (srps) is a very rare congenital anomaly that is classified into four subtypes. it is an autosomal recessive inherited disease. we report a case of this syndrome without a previous family history of congenital defects.

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Journal: :The Journal of bone and joint surgery. British volume 2005
Y S Chooi Y S Siow C S Chong

We report a case of vertebral osteochondroma of C1 causing cord compression and myelopathy in a patient with hereditary multiple exostosis. We highlight the importance of early diagnosis and the appropriate surgery in order to obtain a satisfactory outcome.

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2014
Youssef El Bir Monsef Boufettal

A 32-year old male presented with pain and swelling involving the distal third of the left thigh. He initially noticed a small swelling which eventually increased in size. Patient also had low grade fever without any diurnal variation. There was no past history of antitubercular treatment as well as there was no family history of tuberculosis. There was history of weight loss and loss of appeti...

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Journal: :Archives of Surgery and Clinical Research 2019

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Journal: :Balıkesır Health Sciences Journal 2015

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Journal: :The Laryngoscope 1911

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