-
Je něco špatně v tomto záznamu ?
Clinical and molecular genetic analysis of cytologically uncertain thyroid nodules in patients with thyroid disease
J. Lukas, B. Hintnausova, V. Sykorova, M. Syrucek, M. Maly, D. Lukas, J. Duskova
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2001
Free Medical Journals
od 1998
Medline Complete (EBSCOhost)
od 2007-06-01
ROAD: Directory of Open Access Scholarly Resources
od 2001
PubMed
38058193
DOI
10.5507/bp.2023.048
Knihovny.cz E-zdroje
- MeSH
- dospělí MeSH
- genetické testování MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádory štítné žlázy * genetika MeSH
- retrospektivní studie MeSH
- rizikové faktory MeSH
- senioři MeSH
- tenkojehlová biopsie MeSH
- uzly štítné žlázy * genetika patologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
BACKGROUND: The current requirement is to establish the preoperative diagnosis accurately as possible and to achieve an adequate extent of surgery. The aim of this study was to define the preoperative clinical and molecular genetic risks of malignancy in indeterminate thyroid nodules (Bethesda III and IV) and to determine their impact on the surgical strategy. METHODS: Prospectively retrospective analysis of 287 patients provided the basis of preoperative laboratory examination, sonographic stratification of malignancy risks and cytological findings. Molecular tests focused on pathogenic variants of genes associated with thyroid oncogenesis in cytologically indeterminate nodules (Bethesda III and IV). The evaluation included clinical risk factors: positive family history, radiation exposure and growth in size and/or number of nodules. RESULTS: Preoperative FNAB detected 52 cytologically indeterminate nodules (28.7%) out of 181 patients. Postoperative histopathological examination revealed malignancy in 12 cases (23.7%) and there was no significant difference between Bethesda III and IV categories (P=0.517). Clinical risk factors for malignancy were found in 32 patients (61.5%) and the presence of at least one of them resulted in a clearly higher incidence of malignancy than their absence (31.3% vs. 10.0%, respectively). Pathogenic variants of genes were detected in 12/49 patients in Bethesda III and IV, and in 4 cases (33.3%) thyroid carcinoma was revealed. The rate of malignancies was substantially higher in patients with pathogenic variants than in those without (33.3% vs. 16.2%, respectively). CONCLUSIONS: Our experience implies that molecular genetic testing is one of several decision factors. We will continue to monitor and enlarge our patient cohort to obtain long-term follow-up data.
Department of Biostatistics National Institute of Public Health Prague Czech Republic
Department of Internal Medicine Endocrinology Centre Na Homolce Hospital Prague Czech Republic
Department of Otolaryngology Head and Neck Surgery Na Homolce Hospital Prague Czech Republic
Department of Pathology Na Homolce Hospital Prague Czech Republic
Institute of Endocrinology Department of Molecular Endocrinology Prague Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25008983
- 003
- CZ-PrNML
- 005
- 20250521143018.0
- 007
- ta
- 008
- 250411s2025 xr f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.5507/bp.2023.048 $2 doi
- 035 __
- $a (PubMed)38058193
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Lukáš, Jindřich $u Department of Otolaryngology - Head and Neck Surgery, Na Homolce Hospital, Prague, Czech Republic $u Ear, Nose, and Throat Department Faculty of Medicine in Pilsen, Charles University in Prague, Czech Republic $7 mzk2005269599
- 245 10
- $a Clinical and molecular genetic analysis of cytologically uncertain thyroid nodules in patients with thyroid disease / $c J. Lukas, B. Hintnausova, V. Sykorova, M. Syrucek, M. Maly, D. Lukas, J. Duskova
- 520 9_
- $a BACKGROUND: The current requirement is to establish the preoperative diagnosis accurately as possible and to achieve an adequate extent of surgery. The aim of this study was to define the preoperative clinical and molecular genetic risks of malignancy in indeterminate thyroid nodules (Bethesda III and IV) and to determine their impact on the surgical strategy. METHODS: Prospectively retrospective analysis of 287 patients provided the basis of preoperative laboratory examination, sonographic stratification of malignancy risks and cytological findings. Molecular tests focused on pathogenic variants of genes associated with thyroid oncogenesis in cytologically indeterminate nodules (Bethesda III and IV). The evaluation included clinical risk factors: positive family history, radiation exposure and growth in size and/or number of nodules. RESULTS: Preoperative FNAB detected 52 cytologically indeterminate nodules (28.7%) out of 181 patients. Postoperative histopathological examination revealed malignancy in 12 cases (23.7%) and there was no significant difference between Bethesda III and IV categories (P=0.517). Clinical risk factors for malignancy were found in 32 patients (61.5%) and the presence of at least one of them resulted in a clearly higher incidence of malignancy than their absence (31.3% vs. 10.0%, respectively). Pathogenic variants of genes were detected in 12/49 patients in Bethesda III and IV, and in 4 cases (33.3%) thyroid carcinoma was revealed. The rate of malignancies was substantially higher in patients with pathogenic variants than in those without (33.3% vs. 16.2%, respectively). CONCLUSIONS: Our experience implies that molecular genetic testing is one of several decision factors. We will continue to monitor and enlarge our patient cohort to obtain long-term follow-up data.
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a uzly štítné žlázy $x genetika $x patologie $7 D016606
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a retrospektivní studie $7 D012189
- 650 _2
- $a dospělí $7 D000328
- 650 12
- $a nádory štítné žlázy $x genetika $7 D013964
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a tenkojehlová biopsie $7 D044963
- 650 _2
- $a rizikové faktory $7 D012307
- 650 _2
- $a genetické testování $7 D005820
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Hintnausová, Barbora $u Department of Internal Medicine, Endocrinology Centre, Na Homolce Hospital, Prague, Czech Republic $7 xx0230501
- 700 1_
- $a Sýkorová, Vlasta $u Institute of Endocrinology, Department of Molecular Endocrinology, Prague, Czech Republic $7 xx0118026
- 700 1_
- $a Syrůček, Martin $u Department of Pathology, Na Homolce Hospital, Prague, Czech Republic $7 xx0145890
- 700 1_
- $a Malý, Marek, $d 1961- $u Department of Biostatistics, National Institute of Public Health, Prague, Czech Republic $7 jn20001103265
- 700 1_
- $a Lukáš, David $u Department of General Surgery, 3rd Faculty of Medicine, Charles University and University Hospital Kralovske Vinohrady, Prague, Czech Republic $7 _AN052899
- 700 1_
- $a Dušková, Jaroslava, $d 1952- $u Institute of Pathology, 1st Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic $7 jo2002104714
- 773 0_
- $w MED00012606 $t Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia $x 1804-7521 $g Roč. 169, č. 1 (2025), s. 26-31
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/38058193 $y Pubmed
- 910 __
- $a ABA008 $b A 1502 $c 958 $y p $z 0
- 990 __
- $a 20250411 $b ABA008
- 991 __
- $a 20250521143016 $b ABA008
- 999 __
- $a ok $b bmc $g 2324859 $s 1246061
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2025 $b 169 $c 1 $d 26-31 $e 20231206 $i 1804-7521 $m Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia $n Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub $x MED00012606
- LZP __
- $b NLK124 $a Pubmed-20250411