Zobrazeno 1 - 10
of 167
pro vyhledávání: '"Parachordoma"'
Autor:
Neelam Sood, Kumar Sharad Sinha
Publikováno v:
Journal of Krishna Institute of Medical Sciences University, Vol 5, Iss 2, Pp 140-144 (2016)
Parachordoma is an uncommon tumour of soft tissue of uncertain origin. Recurrence and metastasis are rarely seen. We report two cases with one presenting as recurrent case of pelvic parachordoma in a 45 year old female who presented with painless
Externí odkaz:
https://doaj.org/article/822711c079574bfdac4754d80a629e39
Autor:
Anubha Bajaj
Publikováno v:
Journal of Clinical and Diagnostic Pathology. 1:26-33
Parachordoma is an extremely exceptional, peripherally situated soft tissue neoplasm arising at non axial locations. Also designated as soft tissue “myoepithelioma” or “mixed tumour”, the tumefaction histologically simulates a chordoma of axi
Publikováno v:
Journal of International Advanced Otology, Vol 16, Iss 2, Pp 278-281 (2020)
J Int Adv Otol
J Int Adv Otol
Parachordoma is a rare soft tissue mixed tumor, associated with soft tissue myoepithelioma. It is typically growing slowly and considered less aggressive than other similar soft tissue tumors. However, it does recur sporadically, and on rare occasion
Publikováno v:
Radiology Case Reports
Radiology Case Reports, Vol 14, Iss 1, Pp 94-96 (2019)
Radiology Case Reports, Vol 14, Iss 1, Pp 94-96 (2019)
Parachordoma is a rare entity with less than 50 cases described in the literature. This soft-tissue tumor resembles chordomas as well as extraskeletal myxoid chondrosarcomas and has only recently been fully characterized. Here we describe the case of
Autor:
Mona A. Kandil, Rehab M. Samaka
Publikováno v:
Rare Tumors, Vol 4, Iss 4, Pp e53-e53 (2012)
Parachordoma is an extremely rare soft tissue tumor of unknown lineage. Parachordoma develops most often on the extremities. Only 2 cases have been reported as pelvic parachordoma. A 46-year old Egyptian woman with a huge painful pelvic mass was foun
Externí odkaz:
https://doaj.org/article/08d696c3aba244828077469d2eac122e
Autor:
She-Meng Cheng, Chun-Chao Huang
Publikováno v:
Rare Tumors, Vol 4, Iss 1, Pp e5-e5 (2012)
Parachordoma is an extremely rare entity and there are only about 50 to 60 cases reported, in which there is only one definite pelvic parachordoma. We present a huge well-defined presacral tumor in a 48-year-old woman who has the symptoms of lower ab
Externí odkaz:
https://doaj.org/article/b6a87ee6518e4f239059035ab1bf1be8
Publikováno v:
Turkish Journal of Plastic Surgery. 29:56
Parachordoma is one of the rarest tumors identified, with around fifty cases reported to date. It is reported to have a benign behavior, yet metastatic and fatal cases have been reported. A 63-year-old female patient presented with a subcutaneous mas
Autor:
Kalyan Koti, Monalisa Hui, Rajesh K Ghanta, Shantveer G Uppin, Megha S Uppin, Kanchan K Mukherjee
Publikováno v:
Surgical Neurology International
Background: Parachordomas are rare soft tissue tumors commonly occurring in limbs, chest, Abdomen, and back. The World Health Organization (WHO) classification includes parachordomas in the same group as mixed tumors and myoepitheliomas. Exact histog
Publikováno v:
International Journal of Research in Medical Sciences. 8:4522
Parachordoma is an uncommon tumor of soft tissue and the orign is not clear. This soft tissue tumor resembles chordomas as well as extraskeletal myxoid chondrosarcomas and has only recently been fully characterized. Although it is considered a benign
Publikováno v:
Molecular and Clinical Oncology.