2018
DOI: 10.1136/jclinpath-2018-205337
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Breast tumour resembling tall cell variant of papillary thyroid carcinoma: case presentation (in a patient with Lynch syndrome)

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Cited by 7 publications
(5 citation statements)
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“…As the incidence of TCCRP is low, it is difficult to conduct a valuable retrospective analysis of the disease from independent case reports or small-scale cohort studies. However, we comprehensively reviewed relevant articles (15 in total) published from 2003 to date, and extracted key information including demographic, clinicopathologic, and immunohistochemical data, along with hotspot gene sequencing results (Tables S1,S2), to detect meaningful patterns by expanding the sample size (1)(2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15). After eliminating the repeated cases from among the abovementioned studies, a total of 74 cases (including this present case) remained.…”
Section: Discussionmentioning
confidence: 99%
“…As the incidence of TCCRP is low, it is difficult to conduct a valuable retrospective analysis of the disease from independent case reports or small-scale cohort studies. However, we comprehensively reviewed relevant articles (15 in total) published from 2003 to date, and extracted key information including demographic, clinicopathologic, and immunohistochemical data, along with hotspot gene sequencing results (Tables S1,S2), to detect meaningful patterns by expanding the sample size (1)(2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15). After eliminating the repeated cases from among the abovementioned studies, a total of 74 cases (including this present case) remained.…”
Section: Discussionmentioning
confidence: 99%
“…Bhargava et al employed FISH detection of the ETV-6 gene in one case of TCCRP and secretory carcinoma (yielding negative results) (10). A Solid mammary head, columnar cells, and reversal of nuclear polarity support the diagnosis of TRRCP while S-100 positivity is observed in TCCRP (10,17). Cystic hypersecretory lesions/tumour: This group of diseases needs to be distinguished from TCCRP because of the prominent follicular changes in the thyroid.…”
Section: Discussionmentioning
confidence: 99%
“…TCCRP has been considered to be an invasive tumor with only a few cases reported as carcinoma in situ (still controversial due to improper IHC tests) [1,2,[4][5][6][7][8][9][10][11][12][13][14][15]. In addition, this tumor is underpinned by recurrent nding of IDH2 (hot spot mutations in residue 172) mutations accompanied with genetic alterations in the PI3K signaling pathway, especially PIK3CA [1,16,17].…”
Section: Discussionmentioning
confidence: 99%