Zobrazeno 1 - 10
of 37
pro vyhledávání: '"R. M. TILLMAN"'
Publikováno v:
Sarcoma, Vol 2012 (2012)
Leiomyosarcoma of bone is just one of the variants of spindle cell sarcoma of bone characterised by the expression of desmin and other markers indicating a significant element of smooth muscle in the tumour, without osteoid production we have investi
Externí odkaz:
https://doaj.org/article/dfd71e5f31af4ba5be8844c3fc7aafb3
Autor:
A. M. Malhas, V. P. Sumathi, S. L. James, C. Menna, S. R. Carter, R. M. Tillman, L. Jeys, R. J. Grimer
Publikováno v:
Sarcoma, Vol 2012 (2012)
Low-grade central osteosarcoma (LGCO) is a rare variant of osteosarcoma which is difficult to diagnose. If not treated appropriately, the tumour can recur with higher-grade disease. We reviewed our experience of this condition to try and identify fac
Externí odkaz:
https://doaj.org/article/40adf84393ab4880a11e0655898ebb69
Autor:
J. Haniball, V. P. Sumathi, L.-G. Kindblom, A. Abudu, S. R. Carter, R. M. Tillman, L. Jeys, D. Spooner, D. Peake, R. J. Grimer
Publikováno v:
Sarcoma, Vol 2011 (2011)
Background. This study aimed to investigate prognostic factors for patients with myxoid/round-cell liposarcoma (MRCLS), in particular the significance of the round cell component, and to identify metastatic patterns as well as possibly suggest a suit
Externí odkaz:
https://doaj.org/article/c990aecb5e5242b0b993dd91994e1b83
Publikováno v:
Sarcoma, Vol 2010 (2010)
Introduction. The ‘‘two-week wait’’ was established as a potential means of diagnosing malignant tumours earlier. This paper investigated whether these clinics are leading to earlier diagnosis of malignant soft-tissue lumps. Method. We identi
Externí odkaz:
https://doaj.org/article/254de32741074b4c8638cb6b7560268a
Publikováno v:
Sarcoma, Vol 2009 (2009)
Between 1996 and 2006 a total of 278 patients with soft tissue Leiomyosarcoma were treated at our centre. We identified 16 patients (5.8%) where the tumour directly arose from the blood vessels. These tumours were studied to determine their prognosis
Externí odkaz:
https://doaj.org/article/303283a907e8419fa9406a343cb21673
Autor:
C. R. Chandrasekar, R. J. Grimer, S. R. Carter, R. M. Tillman, A. Abudu, A. M. Davies, V. P. Sumathi
Publikováno v:
Sarcoma, Vol 2008 (2008)
Elastofibroma dorsi is an uncommon benign soft tissue pseudotumour usually located at the lower pole of the scapula, deep to serratus anterior, and often attached to the periosteum of the ribs, presenting with long history of swelling and occasionall
Externí odkaz:
https://doaj.org/article/38fb264d3af74a8d9489b2995b3c42c8
Publikováno v:
J Ultrasound
Groin pain can be caused by a myriad of pathologies. Abnormalities of the rectus femoris are a very rare cause of groin pain; calcific tendinopathy of the direct head is particularly so, with only two case reports in the literature. We report the fir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d1b24e20ec1f029a1732004d1766098
https://doi.org/10.1007/s40477-019-00402-4
https://doi.org/10.1007/s40477-019-00402-4
Publikováno v:
Acta orthopaedica Belgica. 82(2)
We are reporting our experience on patients with -pelvic Ewing's Sarcoma treated in our unit. We retrospectively reviewed a series of patients with non-metastatic pelvic Ewing's sarcoma treated between 1977 and 2009. Patients were classified into thr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d74090664032ccb7619600129a0c60ef
https://pubmed.ncbi.nlm.nih.gov/27682283
https://pubmed.ncbi.nlm.nih.gov/27682283
Publikováno v:
The Journal of Bone and Joint Surgery-American Volume. 87:842-849
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bdd77d4b81d0c230a80290fc82e7d4f
https://doi.org/10.2106/00004623-200504000-00021
https://doi.org/10.2106/00004623-200504000-00021
Autor:
F. Fiorenza, A. Abudu, R. J. Grimer, S. R. Carter, R. M. Tillman, K. Ayoub, D. C. Mangham, A. M. Davies
Publikováno v:
The Journal of Bone and Joint Surgery. British volume. :93-99
We studied 153 patients with non-metastatic chondrosarcoma of bone to determine the risk factors for survival and local tumour control. The minimum follow-up was for five years; 52 patients had axial and 101 appendicular tumours. Surgical treatment w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c89022169d09234118f42a59642d418b
https://doi.org/10.1302/0301-620x.84b1.0840093
https://doi.org/10.1302/0301-620x.84b1.0840093