Parachordoma is a soft tissue tumor that has a light microscopic appearance similar to that of chordoma, and the immunostaining properties of the two tumors are alike. The clinical findings and light microscopy of one case of parachordoma are presented together with ultrastructural observations on this tumor and parachordomas from five additional patients.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.3109/01913129409016297 | DOI Listing |
Ann Coloproctol
February 2022
Division of Colon and Rectal Surgery, Department of Surgery, Mackay Memorial Hospital, Mackay Medical College, Taipei, Taiwan.
Purpose: Hemostasis can be achieved by various methods, but it can be difficult to stop active bleeding in the pelvis. An effective method is described to stop massive active bleeding in the pelvis during colorectal surgery.
Methods: When there were massive bleedings in the pelvis, 3 to 5 Foley catheters were inserted through stab wounds on the abdomen.
J Int Adv Otol
August 2020
Department of ENT, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
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 occasions, it has demonstrated the ability to metastasize.
View Article and Find Full Text PDFIndian J Med Res
July 2019
Department of Respiratory & Critical Care Medicine, Zhengzhou University People's Hospital, Zhengzhou, Henan 450003, PR, China.
Radiol Case Rep
January 2019
Moffitt Cancer Center, 12902 Magnolia Dr., Tampa, FL 33612, USA.
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 a patient with a lower back parachordoma and its subsequent postresection recurrence 9 years after the initial procedure, emphasizing the importance of long-term follow-up in individuals with this diagnosis.
View Article and Find Full Text PDFMol Clin Oncol
August 2018
[This corrects the article DOI: 10.3892/mco.2018.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!