Diagnostic approach in TFE3-rearranged renal cell carcinoma: a multi-institutional international survey.
Adolescent
Adult
Aged
Aged, 80 and over
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
/ genetics
Biomarkers, Tumor
/ genetics
Carcinoma, Renal Cell
/ chemistry
Child
Child, Preschool
Female
Gene Rearrangement
Genetic Predisposition to Disease
Health Care Surveys
Humans
Immunohistochemistry
In Situ Hybridization, Fluorescence
Infant
Kidney Neoplasms
/ chemistry
Male
Middle Aged
Pathologists
Phenotype
Practice Patterns, Physicians'
Predictive Value of Tests
Young Adult
genitourinary pathology
immunohistochemistry
kidney neoplasms
Journal
Journal of clinical pathology
ISSN: 1472-4146
Titre abrégé: J Clin Pathol
Pays: England
ID NLM: 0376601
Informations de publication
Date de publication:
May 2021
May 2021
Historique:
received:
26
12
2020
accepted:
07
01
2021
pubmed:
31
1
2021
medline:
27
4
2021
entrez:
30
1
2021
Statut:
ppublish
Résumé
Transcription factor E3-rearranged renal cell carcinoma (TFE3-RCC) has heterogenous morphologic and immunohistochemical (IHC) features.131 pathologists with genitourinary expertise were invited in an online survey containing 23 questions assessing their experience on TFE3-RCC diagnostic work-up.Fifty (38%) participants completed the survey. 46 of 50 participants reported multiple patterns, most commonly papillary pattern (almost always 9/46, 19.5%; frequently 29/46, 63%). Large epithelioid cells with abundant cytoplasm were the most encountered cytologic feature, with either clear (almost always 10/50, 20%; frequently 34/50, 68%) or eosinophilic (almost always 4/49, 8%; frequently 28/49, 57%) cytology. Strong (3+) or diffuse (>75% of tumour cells) nuclear TFE3 IHC expression was considered diagnostic by 13/46 (28%) and 12/47 (26%) participants, respectively. Main TFE3 IHC issues were the low specificity (16/42, 38%), unreliable staining performance (15/42, 36%) and background staining (12/42, 29%). Most preferred IHC assays other than TFE3, cathepsin K and pancytokeratin were melan A (44/50, 88%), HMB45 (43/50, 86%), carbonic anhydrase IX (41/50, 82%) and CK7 (32/50, 64%). Cut-off for positive
Identifiants
pubmed: 33514585
pii: jclinpath-2020-207372
doi: 10.1136/jclinpath-2020-207372
doi:
Substances chimiques
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
0
Biomarkers, Tumor
0
TFE3 protein, human
0
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
291-299Informations de copyright
© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.