2001
DOI: 10.1053/hupa.2001.28966
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Dedifferentiation of adenoid cystic carcinoma: Report of a case implicating p53 gene mutation

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Cited by 75 publications
(80 citation statements)
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References 14 publications
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“…In the present case, this component was found to be approximately 85% of the area. The high-grade transformed component was the predominant feature in most of the previous cases (10), as in our case.…”
Section: Discussionmentioning
confidence: 49%
See 2 more Smart Citations
“…In the present case, this component was found to be approximately 85% of the area. The high-grade transformed component was the predominant feature in most of the previous cases (10), as in our case.…”
Section: Discussionmentioning
confidence: 49%
“…To our knowledge, there have been only 33 previously reported cases (3,4). The amount of high-grade transformed component in ACC ranges from 10% to 80% (4,10). In the present case, this component was found to be approximately 85% of the area.…”
Section: Discussionmentioning
confidence: 67%
See 1 more Smart Citation
“…Furthermore, the high-grade (''dedifferentiated'') components in ADCC-Ds reported by by Malhotra et al, Chao et al and Moles et al also displayed an absence of myoepithelial differentiation [29][30][31].…”
Section: Discussionmentioning
confidence: 99%
“…Apart from these classic histologic types of adenoid cystic carcinoma, another type, which shows areas of classic adenoid cystic carcinoma with a gradual or sharp transition to areas of high-grade carcinoma has been recently described. To date, about 35 such tumors arising from major and minor salivary glands have been described under different designations, initially as ''hybrid tumors'', between adenoid cystic carcinoma and salivary duct carcinoma [4][5][6][7][8], subsequently as ''dedifferentiated'' adenoid cystic carcinomas [9][10][11][12][13] and most recently as adenoid cystic carcinomas with high-grade transformation [14,15]. The lacrimal gland counterpart of this tumor has, to our knowledge, only been described in two individual case reports [16,17]; two additional cases were included in a recent multiinstitutional histopathologic review of lacrimal gland tumors but not described in detail [2].…”
Section: Introductionmentioning
confidence: 99%