scholarly journals The unstable shoulder: what soft tissue, bony anatomy and biomechanics can teach us

Author(s):  
Lukas N. Muench ◽  
Andreas B. Imhoff
Keyword(s):  
2015 ◽  
Vol 115 ◽  
pp. S825-S826
Author(s):  
K.L. Jakobsen ◽  
J.B.B. Petersen ◽  
L.P. Muren ◽  
M. Hoyer ◽  
H. Lindberg ◽  
...  

2018 ◽  
Vol 47 (3-4) ◽  
pp. 160-176
Author(s):  
G.S. Ibbott

The introduction of image guidance in radiation therapy and its subsequent innovations have revolutionised the delivery of cancer treatment. Modern imaging systems can supplement and often replace the historical practice of relying on external landmarks and laser alignment systems. Rather than depending on markings on the patient’s skin, image-guided radiation therapy (IGRT), using techniques such as computed tomography (CT), cone beam CT, MV on-board imaging (OBI), and kV OBI, allows the patient to be positioned based on the internal anatomy. These advances in technology have enabled more accurate delivery of radiation doses to anatomically complex and temporally changing tumour volumes, while simultaneously sparing surrounding healthy tissues. While these imaging modalities provide excellent bony anatomy image quality, magnetic resonance imaging (MRI) surpasses them in soft tissue image contrast for better visualisation and tracking of soft tissue tumours with no additional radiation dose to the patient. However, the introduction of MRI into a radiotherapy facility has a number of complications, including the influence of the magnetic field on the dose deposition, as well as the effects it can have on dosimetry systems. The development and introduction of these new IGRT techniques will be reviewed, and the benefits and disadvantages of each will be described.


2010 ◽  
Vol 76 (3) ◽  
pp. 767-774 ◽  
Author(s):  
Omar A. Zeidan ◽  
Adam J. Huddleston ◽  
Choonik Lee ◽  
Katja M. Langen ◽  
Patrick A. Kupelian ◽  
...  

Author(s):  
Nicole A. DeVries ◽  
Matthew J. Bollier ◽  
Nicole M. Grosland

Bony anatomy, soft tissue restraints, and the dynamic action of the quadriceps all play a role in maintaining patellar stability throughout knee motion. The medial patellofemoral ligament (MPFL) is the main soft tissue restraint to lateral translation of the patella, and helps guide the patella into the trochlear groove during the first 30° of knee flexion [1]. Studies have shown that the MPFL is the most consistently injured anatomical structure after acute lateral patellar dislocation [2]. Due to the high rate of recurrent episodes of instability following conservative management of acute lateral patellar dislocation, a number of bony and soft tissue procedures have been described to restore patellar stability, including MPFL reconstruction [2].


2007 ◽  
Vol 34 (6Part5) ◽  
pp. 2381-2381
Author(s):  
O Zeidan ◽  
P Kupelian ◽  
K Langen ◽  
R Manon ◽  
S Meeks

Author(s):  
D. C. Swartzendruber ◽  
Norma L. Idoyaga-Vargas

The radionuclide gallium-67 (67Ga) localizes preferentially but not specifically in many human and experimental soft-tissue tumors. Because of this localization, 67Ga is used in clinical trials to detect humar. cancers by external scintiscanning methods. However, the fact that 67Ga does not localize specifically in tumors requires for its eventual clinical usefulness a fuller understanding of the mechanisms that control its deposition in both malignant and normal cells. We have previously reported that 67Ga localizes in lysosomal-like bodies, notably, although not exclusively, in macrophages of the spocytaneous AKR thymoma. Further studies on the uptake of 67Ga by macrophages are needed to determine whether there are factors related to malignancy that might alter the localization of 67Ga in these cells and thus provide clues to discovering the mechanism of 67Ga localization in tumor tissue.


Author(s):  
J. P. Brunschwig ◽  
R. M. McCombs ◽  
R. Mirkovic ◽  
M. Benyesh-Melnick

A new virus, established as a member of the herpesvirus group by electron microscopy, was isolated from spontaneously degenerating cell cultures derived from the kidneys and lungs of two normal tree shrews. The virus was found to replicate best in cells derived from the homologous species. The cells used were a tree shrew cell line, T-23, which was derived from a spontaneous soft tissue sarcoma. The virus did not multiply or did so poorly for a limited number of passages in human, monkey, rodent, rabbit or chick embryo cells. In the T-23 cells, the virus behaved as members of the subgroup B of herpesvirus, in that the virus remained primarily cell associated.


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