Zobrazeno 1 - 10
of 206
pro vyhledávání: '"R J, Grimer"'
Publikováno v:
Sarcoma, Vol 9, Iss 1-2, Pp 33-36 (2005)
Purpose: The purpose of this case report is to bring to light this unusual combination of two rare diseases, namely Neimann-Pick disease Type B and clear cell chondrosarcoma occurring in the same patient. This has not previously been reported in the
Externí odkaz:
https://doaj.org/article/7281ec3de957460f8a50904bc748d534
Publikováno v:
Sarcoma, Vol 8, Iss 1, Pp 1-6 (2004)
Objective. We have investigated whether there is evidence that patients with soft tissue sarcomas do better if treated in a specialist centre compared with district general hospitals.
Externí odkaz:
https://doaj.org/article/c6adcbb836324b68b16f75bcd7b8c463
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:
Jonathan Stevenson, Michael Parry, Lee Jeys, R. J. Grimer, Roger M. Tillman, Magdalena M. Gilg, Adesegun Abudu, Czar Louie Gaston
Publikováno v:
The Bone & Joint Journal. :370-377
AimsThe use of a noninvasive growing endoprosthesis in the management of primary bone tumours in children is well established. However, the efficacy of such a prosthesis in those requiring a revision procedure has yet to be established. The aim of th
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)
We studied 123 patients with malignant peripheral nerve sheath tumours (MPNSTs) between 1979 and 2002. However, 90 occurred sporadically whereas 33 were associated with neurofibromatosis type 1 (NF1). Survival was calculated using Kaplan-Meier surviv
Externí odkaz:
https://doaj.org/article/66c6d0b6ba41431bb208e35069f2bd26
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