2002
DOI: 10.1046/j.1365-2559.2002.01315.x
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Reduced HBME‐1 immunoreactivity of papillary thyroid carcinoma and papillary thyroid carcinoma‐related neoplastic lesions with Hürthle cell and/or apocrine‐like changes

Abstract: All papillary thyroid carcinomas without Hürthle cell or apocrine-like differentiation are reactive for HBME. Hürthle cell tumours and tumours with Hürthle cell or apocrine-like changes show negative or focal reactivity for HBME. Except for this limitation, HBME is a sensitive marker for papillary thyroid carcinoma and tumours with limited nuclear features.

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Cited by 37 publications
(41 citation statements)
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References 19 publications
(31 reference statements)
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“…Thyrotoxic hyperplasia was consistently negative (Rossi et al, 2006) whereas nodular goitres were positive in up to 17% of cases (Ito et al, 2005). Significant reactions were also reported in 25% of thyroiditis (Prasad et al, 2005), 5 -10% of benign follicular tumours devoid of atypical features, and up to 65% with LNFPTC or Hürthle cell features (Mai et al, 2002;Papotti et al, 2005;Prasad et al, 2005;Scognamiglio et al, 2006). The fact that specificity in our study was in the lower range may be due to a high proportion of atypical or Hürthle cell tumours and absence of hyper-functional nodules.…”
Section: Discussionsupporting
confidence: 45%
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“…Thyrotoxic hyperplasia was consistently negative (Rossi et al, 2006) whereas nodular goitres were positive in up to 17% of cases (Ito et al, 2005). Significant reactions were also reported in 25% of thyroiditis (Prasad et al, 2005), 5 -10% of benign follicular tumours devoid of atypical features, and up to 65% with LNFPTC or Hürthle cell features (Mai et al, 2002;Papotti et al, 2005;Prasad et al, 2005;Scognamiglio et al, 2006). The fact that specificity in our study was in the lower range may be due to a high proportion of atypical or Hürthle cell tumours and absence of hyper-functional nodules.…”
Section: Discussionsupporting
confidence: 45%
“…However, overall results obtained on fresh tissue, including our study, and cell blocks are rather concordant. The sensitivity of HBME-1 staining was excellent (490%) for classical PC (van Hoeven et al, 1998;Ito et al, 2005;Rossi et al, 2005), disappointing for PCFV, and poor (o65%) for follicular and undifferentiated cancers (Cheung et al, 2001;Mai et al, 2002;Ito et al, 2005;Prasad et al, 2005;Saggiorato et al, 2005). The reported specificity of HBME-1 staining ranged from 70% to more than 90% (Cheung et al, 2001;Prasad et al, 2005;Saggiorato et al, 2005).…”
Section: Discussionmentioning
confidence: 99%
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“…In recent years, many papers have been published on the identification of protein markers to improve the differential diagnosis of thyroid lesions, using both a candidate marker and an unbiased approach (4)(5)(6)(7)(8)(9)(10)(11)(12). Despite the considerable variability in the outcomes of these studies, some promising protein markers for the differential diagnosis of thyroid neoplastic lesions have emerged, including galectin-3 (Gal-3) (4,(12)(13)(14)(15)(16)(17)(18) and Hector Battifora mesothelial (HBME-1) (18)(19)(20)(21)(22)(23). has been found to be strongly and diffusely expressed in papillary thyroid carcinoma (PTC), whereas it is heterogeneously expressed in follicular thyroid carcinoma (FTC) and absent or focally expressed in follicular adenoma (FA) (18,(24)(25)(26)(27)(28)(29).…”
Section: Introductionmentioning
confidence: 99%
“…Depending on the severity of these changes and the bias of the observer, terms such as atypical adenoma, 'hybrid' carcinoma, and-more recentlywell-differentiated carcinoma not otherwise specified were proposed. [1][2][3][4][5] In a recent editorial from the Chernobyl Pathologists Group the suggestion was made to label tumors with 'borderline' features as well-differentiated tumor of uncertain malignant potential (WDT-UMP) in the presence of questionable papillary carcinoma-type nuclear changes with or without questionable capsular penetration, or follicular tumor of uncertain malignant potential (FT-UMP) in the presence of questionable capsular penetration without nuclear changes. 6,7 Several immunocytochemical markers of malignancy have been claimed to be useful to distinguish follicular adenoma from carcinoma and also to identify papillary carcinoma and its variants, both in surgical and cytological specimens.…”
mentioning
confidence: 99%