Soft tissue sarcomas of the adult head and neck

1986 ◽  
Vol 77 (5) ◽  
pp. 868
Author(s):  
J A Greager
2020 ◽  
Vol 108 (3) ◽  
pp. e13-e14
Author(s):  
R.A. Abu-Hijlih ◽  
F.J. Abuhijla ◽  
I. Mohammed ◽  
H. Halalsheh ◽  
A. Almousa ◽  
...  

1986 ◽  
Vol 19 (3) ◽  
pp. 565-572
Author(s):  
John A. Greager ◽  
Tapas K. Das Gupta

Sarcoma ◽  
2008 ◽  
Vol 2008 ◽  
pp. 1-5 ◽  
Author(s):  
Rabindra P. Singh ◽  
Robert J. Grimer ◽  
Nabina Bhujel ◽  
Simon R. Carter ◽  
Roger M. Tillman ◽  
...  

We have retrospectively analysed the experience of a musculoskeletal oncological unit in the management of adult head and neck soft tissue sarcomas from 1990 to 2005. Thirty-six patients were seen, of whom 24 were treated at this unit, the remainder only receiving advice. The median age of the patients was 46 years. Most of the sarcomas were deep and of high or intermediate grade with a median size of 5.5 cm. Eleven different histological subtypes were identified. Wide excision was possible only in 21% of the cases. 42% of the patients developed local recurrence and 42% developed metastatic disease usually in the lungs. Overall survival was 49% at 5 years. Tumour size was the most important prognostic factor. Adult head and neck soft tissue sarcomas have a high mortality rate with a high risk of local recurrence and metastatic disease. The rarity of the disease would suggest that centralisation of care could lead to increased expertise and better outcomes.


Cancer ◽  
1985 ◽  
Vol 56 (4) ◽  
pp. 820-824 ◽  
Author(s):  
John A. Greager ◽  
Minu K. Patel ◽  
Henry A. Briele ◽  
Michael J. Walker ◽  
Tapas K. Das Gupta

2017 ◽  
Vol 16 (1) ◽  
pp. 69-76 ◽  
Author(s):  
Salman Amiruddin ◽  
Mohd Razif Muhamad Yunus ◽  
Marina Mat Baki

Background: Head and neck tissue sarcoma are rare with potential high morbidity and mortality. The purpose of the present study was to present these cases and determine the optimal treatment for adult patients with head and neck soft tissue sarcomas.Methods: It is a retrospective study of adult head and neck soft tissue sarcoma conducted in the Department of Otorhinolaryngology at Universiti Kebangsaan Malaysia Medical Centre (UKMMC) which is one of the national referral center within the period of 16 years from 1998 till 2014.Results: Fourteen cases were reviewed in which7 histopathological variations of soft tissue sarcomas were identified. Local control after surgery alone or combined with radiotherapy was obtained in 50 % of the patients which is influenced by histologic grade, tumor size, and surgical margins. Patients with high-grade tumors or positive margins have improved local control if adjuvant radiotherapy is used. Distant metastases occurred in 14.2 % of patients and the 5-year survival rate was 50 %.Conclusions: The optimal treatment for adult head and neck soft tissue sarcomas is surgery. Adjuvant radiotherapy improves outcomes for those with high-grade tumors or positive margins.Bangladesh Journal of Medical Science Vol.16(1) 2017 p.69-76


2005 ◽  
Vol 28 (3) ◽  
pp. 259-263 ◽  
Author(s):  
Susie A. Chen ◽  
Christopher G. Morris ◽  
Robert J. Amdur ◽  
John W. Werning ◽  
Douglas B. Villaret ◽  
...  

Head & Neck ◽  
2005 ◽  
Vol 27 (10) ◽  
pp. 916-922 ◽  
Author(s):  
William M. Mendenhall ◽  
Charles M. Mendenhall ◽  
John W. Werning ◽  
Charles E. Riggs ◽  
Nancy Price Mendenhall

2000 ◽  
Vol 5 (4) ◽  
pp. 269-275
Author(s):  
T. Shouman ◽  
M. Gameel ◽  
A. Attia ◽  
S. A. El-Aziz ◽  
N. Mohamed

2017 ◽  
Vol 13 (01) ◽  
pp. 01
Author(s):  
Ignacio Mendoza ◽  
Ilson Sepúlveda ◽  
Geraldine Ayres ◽  
◽  
◽  
...  

Synovial sarcoma (SS) represents about 10% of all soft tissue sarcomas. It is believed that its origin would be found in cells that are related neither to ultrastructural nor to histological features of the synovial tissue. Head and neck is very rarely affected, with the lower extremities being most frequent. Complete resection with or without radiotherapy and chemotherapy is currently considered the best available therapy. This time we present the case of a patient with SS located in the infratemporal fossa, its diagnosis, treatment and evolution. According to our knowledge it is the first reported case in South America.


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