Synovial sarcoma of carotid space
Samo za registrovane korisnike
2012
Autori
Krstić, Viktor A.Milosavljević, Miloš Z.
Mitrović, Slobodanka
Azanjac, Goran Lj.
Knežević, Milan G.
Konstantinović, Vitomir
Nedović, Jasmina R.
Članak u časopisu (Objavljena verzija)
Metapodaci
Prikaz svih podataka o dokumentuApstrakt
Synovial sarcomas are malignant tumors of mesenchymal origin, extremely rarely located in the area of the head and neck. Histologically they can be monophasic, biphasic or poorly differentiated with numerous differential diagnostic dilemmas. A 54-year-old male with synovial sarcoma of the carotid space is presented. The patient refused suggested postoperative radiotherapy and, nine months after the primary surgery, local relapse was verified. Following surgical resection of the local relapse, postoperative radiotherapy treatment was utilized. Ten months after the second surgery, secondary deposits in the lungs were radiographically confirmed, and local recurrence was noticed again. Treatment was continued with symptomatic therapy and eleven months later patient died. Synovial sarcomas of the carotid space are extremely rare, with complex surgical approaches and pathohistological differential diagnostic dilemmas. Diagnosis requires determination of the immunophenotype of the tumor cells..., whereas therapy requires an aggressive surgical approach and postoperative radiotherapy.
Ključne reči:
Synovial sarcoma / Head and neck / Surgery / ImmunohistochemistryIzvor:
Central European Journal of Medicine, 2012, 7, 4, 497-502Izdavač:
- Versita, Warsaw
DOI: 10.2478/s11536-012-0004-1
ISSN: 1895-1058
WoS: 000304396400012
Scopus: 2-s2.0-84865782576
Kolekcije
Institucija/grupa
Stomatološki fakultetTY - JOUR AU - Krstić, Viktor A. AU - Milosavljević, Miloš Z. AU - Mitrović, Slobodanka AU - Azanjac, Goran Lj. AU - Knežević, Milan G. AU - Konstantinović, Vitomir AU - Nedović, Jasmina R. PY - 2012 UR - https://smile.stomf.bg.ac.rs/handle/123456789/1739 AB - Synovial sarcomas are malignant tumors of mesenchymal origin, extremely rarely located in the area of the head and neck. Histologically they can be monophasic, biphasic or poorly differentiated with numerous differential diagnostic dilemmas. A 54-year-old male with synovial sarcoma of the carotid space is presented. The patient refused suggested postoperative radiotherapy and, nine months after the primary surgery, local relapse was verified. Following surgical resection of the local relapse, postoperative radiotherapy treatment was utilized. Ten months after the second surgery, secondary deposits in the lungs were radiographically confirmed, and local recurrence was noticed again. Treatment was continued with symptomatic therapy and eleven months later patient died. Synovial sarcomas of the carotid space are extremely rare, with complex surgical approaches and pathohistological differential diagnostic dilemmas. Diagnosis requires determination of the immunophenotype of the tumor cells, whereas therapy requires an aggressive surgical approach and postoperative radiotherapy. PB - Versita, Warsaw T2 - Central European Journal of Medicine T1 - Synovial sarcoma of carotid space VL - 7 IS - 4 SP - 497 EP - 502 DO - 10.2478/s11536-012-0004-1 ER -
@article{ author = "Krstić, Viktor A. and Milosavljević, Miloš Z. and Mitrović, Slobodanka and Azanjac, Goran Lj. and Knežević, Milan G. and Konstantinović, Vitomir and Nedović, Jasmina R.", year = "2012", abstract = "Synovial sarcomas are malignant tumors of mesenchymal origin, extremely rarely located in the area of the head and neck. Histologically they can be monophasic, biphasic or poorly differentiated with numerous differential diagnostic dilemmas. A 54-year-old male with synovial sarcoma of the carotid space is presented. The patient refused suggested postoperative radiotherapy and, nine months after the primary surgery, local relapse was verified. Following surgical resection of the local relapse, postoperative radiotherapy treatment was utilized. Ten months after the second surgery, secondary deposits in the lungs were radiographically confirmed, and local recurrence was noticed again. Treatment was continued with symptomatic therapy and eleven months later patient died. Synovial sarcomas of the carotid space are extremely rare, with complex surgical approaches and pathohistological differential diagnostic dilemmas. Diagnosis requires determination of the immunophenotype of the tumor cells, whereas therapy requires an aggressive surgical approach and postoperative radiotherapy.", publisher = "Versita, Warsaw", journal = "Central European Journal of Medicine", title = "Synovial sarcoma of carotid space", volume = "7", number = "4", pages = "497-502", doi = "10.2478/s11536-012-0004-1" }
Krstić, V. A., Milosavljević, M. Z., Mitrović, S., Azanjac, G. Lj., Knežević, M. G., Konstantinović, V.,& Nedović, J. R.. (2012). Synovial sarcoma of carotid space. in Central European Journal of Medicine Versita, Warsaw., 7(4), 497-502. https://doi.org/10.2478/s11536-012-0004-1
Krstić VA, Milosavljević MZ, Mitrović S, Azanjac GL, Knežević MG, Konstantinović V, Nedović JR. Synovial sarcoma of carotid space. in Central European Journal of Medicine. 2012;7(4):497-502. doi:10.2478/s11536-012-0004-1 .
Krstić, Viktor A., Milosavljević, Miloš Z., Mitrović, Slobodanka, Azanjac, Goran Lj., Knežević, Milan G., Konstantinović, Vitomir, Nedović, Jasmina R., "Synovial sarcoma of carotid space" in Central European Journal of Medicine, 7, no. 4 (2012):497-502, https://doi.org/10.2478/s11536-012-0004-1 . .