Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 1
2015 1
2016 2
2017 1
2019 1
2020 2
2021 5
2022 5
2023 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

14 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Laryngeal Soft Tissue Sarcoma"
Page 1
Pediatric laryngeal sarcoma: Systematic review and pooled analysis.
Mur TA, Pellegrini WR, Jaleel Z, Edwards HA, Levi JR. Mur TA, et al. Int J Pediatr Otorhinolaryngol. 2020 Dec;139:110471. doi: 10.1016/j.ijporl.2020.110471. Epub 2020 Oct 23. Int J Pediatr Otorhinolaryngol. 2020. PMID: 33120103 Review.
To date, there are no analyses evaluating treatment of pediatric sarcoma within the larynx specifically. METHODS: A structured literature review following PRISMA guidelines was preformed to identify case reports of pediatric (age 17 and younger) laryngeal
To date, there are no analyses evaluating treatment of pediatric sarcoma within the larynx specifically. METHODS: A structured …
Laryngeal soft tissue sarcoma: Systematic review and individual patient data analysis of 300 cases.
Ramdulari AV, Izzuddeen Y, Benson R, Mallick S, Venkatesulu B, Giridhar P. Ramdulari AV, et al. Head Neck. 2021 May;43(5):1421-1427. doi: 10.1002/hed.26604. Epub 2021 Jan 14. Head Neck. 2021. PMID: 33448036
BACKGROUND: Laryngeal sarcoma is rare. We performed a systematic review and individual patient analysis to evaluate the patterns of care, prognostic factors, and role of radiotherapy in laryngeal soft tissue sarcoma. ...An individual pati …
BACKGROUND: Laryngeal sarcoma is rare. We performed a systematic review and individual patient analysis to evaluate the patter …
Imaging features of laryngeal chondrosarcomas: A case series and systematic review.
Baba A, Kurokawa R, Kurokawa M, Ota Y, Lobo R, Srinivasan A. Baba A, et al. J Neuroimaging. 2022 Mar;32(2):213-222. doi: 10.1111/jon.12963. Epub 2022 Jan 12. J Neuroimaging. 2022. PMID: 35019171 Review.
BACKGROUND AND PURPOSE: To comprehensively summarize the characteristics of radiological findings of laryngeal conventional chondrosarcomas. METHODS: We included patients with pathologically proven laryngeal conventional chondrosarcomas with CT and /or MRI, includin …
BACKGROUND AND PURPOSE: To comprehensively summarize the characteristics of radiological findings of laryngeal conventional chondrosa …
Survival outcomes in laryngeal chondrosarcoma: a systematic review.
Álvarez-Calderón-Iglesias O, Pérez-Sayáns M, Hurtado-Ruzza R, Lorenzo-Pouso A, Chamorro-Petronacci C. Álvarez-Calderón-Iglesias O, et al. Acta Otorhinolaryngol Ital. 2022 Dec;42(6):502-515. doi: 10.14639/0392-100X-N1912. Acta Otorhinolaryngol Ital. 2022. PMID: 36654516 Free PMC article. Review.
Laryngeal chondrosarcomas (LCS) are rare lesions that behave as locally aggressive tumours, producing symptoms such as dysphonia, dyspnoea, dysphagia and hoarseness. ...In December 2020, a systematic review was performed following Preferred Reporting Items for Systematic R
Laryngeal chondrosarcomas (LCS) are rare lesions that behave as locally aggressive tumours, producing symptoms such as dysphonia, dys
Laryngeal Synovial Sarcoma: A Systematic Review of the Last 40 Years of Reported Cases.
Shein G, Sandhu G, Potter A, Loo C, Jacobson I, Anazodo A. Shein G, et al. Ear Nose Throat J. 2021 Feb;100(2):NP93-NP104. doi: 10.1177/0145561319850697. Epub 2019 Jul 16. Ear Nose Throat J. 2021. PMID: 31309846 Free article.
Primary laryngeal synovial sarcoma is an extremely rare tumor predominantly affecting young adults. ...A total of 39 cases were reviewed from 32 studies in the data extraction. The average age at the time of laryngeal synovial sarcoma diagnosis was 32 …
Primary laryngeal synovial sarcoma is an extremely rare tumor predominantly affecting young adults. ...A total of 39 cases wer …
Laryngeal chondrosarcoma: A systematic review of 592 cases.
Chin OY, Dubal PM, Sheikh AB, Unsal AA, Park RC, Baredes S, Eloy JA. Chin OY, et al. Laryngoscope. 2017 Feb;127(2):430-439. doi: 10.1002/lary.26068. Epub 2016 Jun 12. Laryngoscope. 2017. PMID: 27291822 Review.
OBJECTIVES/HYPOTHESIS: Laryngeal chondrosarcomas are rare entities that arise from the cartilaginous structures of the larynx, including the cricoid, thyroid cartilage, epiglottis, and arytenoid cartilages. These tumors represent a minority of malignancies involving …
OBJECTIVES/HYPOTHESIS: Laryngeal chondrosarcomas are rare entities that arise from the cartilaginous structures of the larynx, …
Carcinosarcomas of the larynx: systematic review of the literature of a rare nosologic entity.
Colizza A, Gilardi A, Greco A, Cialente F, Zoccali F, Ralli M, Minni A, de Vincentiis M. Colizza A, et al. Eur Arch Otorhinolaryngol. 2022 Mar;279(3):1167-1173. doi: 10.1007/s00405-021-07027-6. Epub 2021 Aug 5. Eur Arch Otorhinolaryngol. 2022. PMID: 34351467 Free PMC article. Review.
The aim of this study was to systematically review the literature of SpCC of larynx and report epidemiologic, clinicopathologic and main therapeutic approaches for this entity. ...The clinical and pathological staging were recalculated according to the Eight Edition of AJC …
The aim of this study was to systematically review the literature of SpCC of larynx and report epidemiologic, clinicopathologic and m …
Systematic review and meta-analysis of cancer risks in relation to environmental waste incinerator emissions: a meta-analysis of case-control and cohort studies.
Baek K, Park JT, Kwak K. Baek K, et al. Epidemiol Health. 2022;44:e2022070. doi: 10.4178/epih.e2022070. Epub 2022 Sep 1. Epidemiol Health. 2022. PMID: 36097807 Free PMC article.
The pooled effect size was not significant for breast, colorectal, liver, lung, lymphohematopoietic, stomach, bladder, central nervous system, and laryngeal cancers, non-Hodgkin lymphoma, sarcoma, leukemia, and all cancers. In the subgroup analysis, the pooled effec …
The pooled effect size was not significant for breast, colorectal, liver, lung, lymphohematopoietic, stomach, bladder, central nervous syste …
Pediatric laryngeal inflammatory myofibroblastic tumour: Case report and systematic review of the literature.
Smaily H, Cherfane P, Matar N. Smaily H, et al. Auris Nasus Larynx. 2021 Dec;48(6):1047-1053. doi: 10.1016/j.anl.2020.08.018. Epub 2020 Aug 30. Auris Nasus Larynx. 2021. PMID: 32878712
INTRODUCTION: Inflammatory myofibroblastic tumours (IMT) are rare benign neoplasms in the pediatric population, found most frequently in the lungs with rare reports of laryngeal involvement. The aim of this paper is to present a clinical case of laryngeal IMT follow …
INTRODUCTION: Inflammatory myofibroblastic tumours (IMT) are rare benign neoplasms in the pediatric population, found most frequently in the …
Kaposi Sarcoma of the Larynx: A Systematic Review.
Barron K, Omiunu A, Celidonio J, Cruz-Mullane A, Din-Lovinescu C, Chemas-Velez MM, Baredes S, Eloy JA, Fang CH. Barron K, et al. Otolaryngol Head Neck Surg. 2023 Mar;168(3):269-281. doi: 10.1177/01945998221105059. Epub 2023 Jan 24. Otolaryngol Head Neck Surg. 2023. PMID: 35671149
OBJECTIVE: Kaposi sarcoma (KS) of the larynx is a rare disease with few cases reported in the literature. This study aims to provide a comprehensive review of laryngeal KS, including patient characteristics, treatment, and clinical outcomes. ...
OBJECTIVE: Kaposi sarcoma (KS) of the larynx is a rare disease with few cases reported in the literature. This study aims to p …
14 results