Zobrazeno 1 - 10
of 89
pro vyhledávání: '"disappearing bone disease"'
Publikováno v:
Malaysian Orthopaedic Journal, Vol 10, Iss 3, Pp 42-45 (2016)
Multicentric disappearing bone disease, or Gorham disease, is a rare entity. A middle age woman, presented to us with left sided antalgic gait and severe bony deformity of her left knee. Radiograph revealed massive bone defect of the medial condyle o
Externí odkaz:
https://doaj.org/article/571806b1823a4f83b5066de2b0cad71f
Akademický článek
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Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 11, Pp ZD25-ZD27 (2015)
Massive osteolysis is a rare idiopathic bone disease resulting in progressive destruction of bone. Considering the rarity of encountering this fascinating bone disease, it is often misinterpreted as some other osteolytic disease. Hence, we present a
Externí odkaz:
https://doaj.org/article/49de74b8c1694a2f8c044a9480195d35
Publikováno v:
Interdisciplinary Neurosurgery, Vol 17, Iss, Pp 79-83 (2019)
Disappearing bone disease, also known as Gorham's disease, is a rare idiopathic musculoskeletal disorder characterized by clinical and radiological disappearance of bone caused by a proliferation of non-neoplastic vascular tissue. The disease was fir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab30763e7296a5e9af632ab86365284a
http://www.sciencedirect.com/science/article/pii/S2214751918302111
http://www.sciencedirect.com/science/article/pii/S2214751918302111
Kniha
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Publikováno v:
Malaysian Orthopaedic Journal, Vol 10, Iss 3, Pp 42-45 (2016)
Malaysian Orthopaedic Journal
Malaysian Orthopaedic Journal
Multicentric disappearing bone disease, or Gorham disease, is a rare entity. A middle age woman, presented to us with left sided antalgic gait and severe bony deformity of her left knee. Radiograph revealed massive bone defect of the medial condyle o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccd2ff98c6723f9f8b342ceb87d4bda0
https://doi.org/10.5704/moj.1611.004
https://doi.org/10.5704/moj.1611.004
Publikováno v:
Journal of Surgical Case Reports
Disappearing bone disease is a rare disorder that causes spontaneous and progressive osteolysis and proliferation of lymphatic tissue and blood vessels. It is debilitating and there is evidence of mortality in reported cases including those affecting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea679c0d087e4f6e934e61e3c2b05620
https://doi.org/10.1093/jscr/rjx025
https://doi.org/10.1093/jscr/rjx025
Autor:
Fatih Kantarci, Harun Ozer, Muharrem Babacan, Mustafa Ozbayrak, Kemal Harmanci, Mehmet Halit Yilmaz, Sergülen Dervişoğlu
Publikováno v:
Korean Journal of Radiology
A patient with a 2-year history of pain in the left arm, and decreased strengths unrelieved by non-steroidal anti-inflammatory therapy, was being referred for repeating radiography. The radiologic examinations have demonstrated a unique pattern of no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b74433c5b2aaadc35ce19b493fc5e77b
http://europepmc.org/articles/PMC3835643
http://europepmc.org/articles/PMC3835643
Autor:
Reiner Bartl, Christoph Bartl
Publikováno v:
Bone Disorders ISBN: 9783319291802
The Osteoporosis Manual ISBN: 9783030007300
The Osteoporosis Manual ISBN: 9783030007300
This syndrome is also known as massive osteolysis, disappearing bone disease and phantom bone.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::678a15cd7163cc4dab82fc83e897d8cc
https://doi.org/10.1007/978-3-319-29182-6_67
https://doi.org/10.1007/978-3-319-29182-6_67
Publikováno v:
Journal of Clinical and Experimental Dentistry. :e328-e335
Vanishing bone disease is a very rare, peculiar destructive condition of the skeletal system resulting in spontaneous and progressive resorption and disappearance of osseous structures with replacement by vascular, fibrous connective tissue. Children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69d9a38cdeae93dab0f93415adf7f125
https://doi.org/10.4317/jced.3.e328
https://doi.org/10.4317/jced.3.e328