2020
DOI: 10.1016/j.wneu.2020.01.130
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SMARCB1-Deficient Sinonasal Carcinoma: Systematic Review and Case Report

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Cited by 19 publications
(17 citation statements)
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“…Of the remaining 192 patients, 72 patients whose individual baseline patient characteristics, treatment details, and survival outcomes could not be identified and verified [2,16,19,20,23,[28][29][30]34,35,38], and they were thus not included into our survival analysis. As a result, only 120 patients with data availability of baseline patient characteristics, disease stage, and survival outcomes in 25 publications were included for survival and prognostic factor analyses [1,2,11,[13][14][15][16][17]19,[21][22][23][24][25][26][27][31][32][33]36,37,[39][40][41][42].…”
Section: Search Strategy Resultsmentioning
confidence: 99%
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“…Of the remaining 192 patients, 72 patients whose individual baseline patient characteristics, treatment details, and survival outcomes could not be identified and verified [2,16,19,20,23,[28][29][30]34,35,38], and they were thus not included into our survival analysis. As a result, only 120 patients with data availability of baseline patient characteristics, disease stage, and survival outcomes in 25 publications were included for survival and prognostic factor analyses [1,2,11,[13][14][15][16][17]19,[21][22][23][24][25][26][27][31][32][33]36,37,[39][40][41][42].…”
Section: Search Strategy Resultsmentioning
confidence: 99%
“…Here, we have presented the largest systematic review of patient characteristics, treatment details, and survival outcomes of patients with SMARCB1-deficient sinonasal carcinoma, among the two previously published which did not include all reported cases [29,42]. SMARCB-1 deficient sinonasal carcinoma, first reported in 2014, remains one of the rarest and most poorly understood sinonasal malignancies.…”
Section: Discussionmentioning
confidence: 99%
“…Nasal cavity and paranasal sinus cancer accounts for about 3%-5% of the entire head and neck tumors, and SDSC is even rarer. The latest literature reports about 82 cases of this disease in the world [3], The disease was reported for the first time in my country in 2018, and currently there are only 2 reports in Chinese search [4,5]. In 2019, Goda et al [6] reported the disease for the first time in Japan.…”
Section: Discussionmentioning
confidence: 99%
“…O carcinoma sinosal SMARCB1-deficiente representa um subtipo de carcinoma sinosal pouco diferenciado/indiferenciado raro, recentemente descoberto, de elevada agressividade e propensão à metástase, dispondo de apenas 89 casos descritos na literatura, atingindo pacientes de 19 a 89 anos, com leve predileção por homens [1][2][3][4] . Este tumor é resultante da inativação do gene SMARCB1, visualizada em exames imunohistoquímicos pela perda completa da expressão de SMARCB1 (INI1), proteína envolvida no remodelamento de cromatina e regulação transcripcional, conhecida pela sua atividade de supressão tumoral 2,3 .…”
Section: Introductionunclassified