9 results on '"Betka, J."'
Search Results
2. High incidence of occult familial SDHD cases amongst Czech patients with head and neck paragangliomas.
- Author
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Guha A, Vicha A, Zelinka T, Kana M, Musil Z, Pacak K, Betka J, Chovanec M, Plzak J, and Boucek J
- Subjects
- Adult, Female, Humans, Male, Czech Republic epidemiology, Incidence, Mutation, Succinate Dehydrogenase genetics, Adolescent, Young Adult, Middle Aged, Aged, Paraganglioma epidemiology, Paraganglioma genetics, Paraganglioma diagnosis, Paraganglioma, Extra-Adrenal
- Abstract
Introduction: Head and neck paragangliomas (HNPGLs) are rare neuroendocrine tumors, which are mostly benign in nature. Amongst all genes, Succinate Dehydrogenase Subunit D ( SDHD ) is the most commonly mutated in familial HNPGLs. In about 30% of HNPGLs, germline mutations in SDHD can also occur in the absence of positive family history, thus giving rise to "occult familial" cases. Our aim was to evaluate the pattern of SDHD germline mutations in Czech patients with HNPGLs., Materials and Methods: We analyzed a total of 105 patients with HNPGLs from the Otorhinolaryngology departments of 2 tertiary centers between 2006 - 2021. All underwent complex diagnostic work-up and were also consented for genetic analysis., Results: Eighty patients aged 13-76 years were included; around 60% with multiple PGLs were males. Carotid body tumor was the most frequently diagnosed tumor. Germline SDHD mutation was found in only 12% of the Czech patients; approximately 78% of those harboring the mutation had negative family history. The mutation traits had higher affiliation for multiple tumors with nearly 70% patients of ≤ 40 years of age., Conclusion: An SDHD mutation variant was shared amongst unrelated patients but no founder-effect was established. Our findings confirmed that the pattern of SDHD mutation distribution amongst HNPGLs in Czech Republic differs from most studies worldwide., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision., (Copyright © 2023 Guha, Vicha, Zelinka, Kana, Musil, Pacak, Betka, Chovanec, Plzak and Boucek.)
- Published
- 2023
- Full Text
- View/download PDF
3. [30 years of the cochlear implantations in the Czech Republic].
- Author
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Bouček J, Kluh J, Čada Z, Vokřál J, Černý L, Tichý T, Skřivan J, Betka J, and Plzák J
- Subjects
- Czech Republic, Humans, Cochlear Implantation, Cochlear Implants
- Abstract
Cochlear implant is the unique sensory neuroprosthesis and still the only one used in clinical praxis. The function of the inner ear is replaced with direct electrical stimulation of the cochlear nerve. It is 30 years since the first cochlear implantation has been performed with the Czech single-channel cochlear neuroprosthesis. There are more than one thousand users of cochlear implants in the Czech Republic nowadays. Cochlear implants have become a standard of care of patients with severe hearing loss. It allows user inclusion to the society with only a minimum of obstacles.Key words: cochlear implant, history, neuroprosthesis, severe hearing loss.
- Published
- 2017
4. A 3-bp Deletion VK600-1E in the BRAF Gene Detected in a Young Woman with Papillary Thyroid Carcinoma.
- Author
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Dvorakova S, Sykorova V, Vaclavikova E, Sykorova P, Vlcek P, Kodetova D, Lastuvka P, Betka J, Mokrejs M, Vcelak J, and Bendlova B
- Subjects
- Adult, Carcinoma, Papillary, Czech Republic, Female, Humans, Proto-Oncogene Mas, Sequence Deletion, Thyroid Cancer, Papillary, Carcinoma genetics, Proto-Oncogene Proteins B-raf genetics, Thyroid Neoplasms genetics
- Abstract
Papillary thyroid cancer (PTC) derived from follicular cells is a frequent thyroid tumor. The incidence of this type of malignancy is still growing worldwide. Several major genetic causes are recognized to cause PTC-mutations in the BRAF and RAS genes or rearrangements with the RET proto-oncogene. The most common genetic change found in PTC is a V600E mutation in the BRAF gene presented in 36-69 % of all PTC cases. For routine purposes, several methods were developed to selectively detect only this mutation. However, these methods miss other mutations in the BRAF gene located elsewhere. We focused on the analysis of the exon 15 of the BRAF gene by next-generation sequencing. Here we report a three nucleotide deletion VK600-1E in one patient and present this finding in the context of 13 previously described PTC cases with this deletion. Our patient is the second youngest one among the reported cases. Clinical features of PTC patients with VK600-1E are summarized. For the future, it is important to evaluate genotype-phenotype characteristics of patients with rare BRAF mutations and to follow up them for years.
- Published
- 2015
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5. BRAFV600E mutation in the pathogenesis of a large series of papillary thyroid carcinoma in Czech Republic.
- Author
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Sykorova V, Dvorakova S, Ryska A, Vcelak J, Vaclavikova E, Laco J, Kodetova D, Kodet R, Cibula A, Duskova J, Hlobilkova A, Astl J, Vesely D, Betka J, Hoch J, Smutny S, Cap J, Vlcek P, Novak Z, and Bendlova B
- Subjects
- Adult, Age Factors, Aged, Aged, 80 and over, Carcinoma, Papillary epidemiology, Carcinoma, Papillary pathology, Chernobyl Nuclear Accident, Codon genetics, Czech Republic epidemiology, DNA, Neoplasm biosynthesis, DNA, Neoplasm genetics, Exons genetics, Female, Gene Frequency, Humans, Male, Middle Aged, Mutation physiology, Neoplasm Invasiveness genetics, Polymorphism, Single-Stranded Conformational genetics, Reverse Transcriptase Polymerase Chain Reaction, Thyroid Neoplasms epidemiology, Thyroid Neoplasms pathology, Carcinoma, Papillary genetics, Proto-Oncogene Proteins B-raf genetics, Thyroid Neoplasms genetics
- Abstract
Background: Activating point mutation of the BRAF gene, the most common genetic alteration reported in papillary thyroid carcinomas (PTC), has been associated with poor prognostic characteristics., Aim: Our objective was to determine the frequency of BRAFV600E mutation in PTC tumor tissues from the period 1960-2007 and to correlate it with clinicopathological parameters., Subjects and Methods: DNAs were extracted from 242 PTCs, 23 sporadic medullary carcinomas, one anaplastic carcinoma and 6 poorly differentiated carcinomas. The presence of BRAFV600E mutation was determined using single strand conformation polymorphism method and verified by direct sequencing., Results: BRAFV600E mutation was detected in 81 of 242 PTCs (33.5%), in one of 6 poorly differentiated carcinomas (16.7%) and in anaplastic carcinoma. BRAFV600E mutation was much less frequent in the follicular variant compared to classical variant and mixed follicular- classical variant of PTCs (p=0.001). BRAFV600E mutation was significantly associated with presence of nodal metastasis (p=0.029), more advanced TNM stage (p=0.014) and recurrence of disease (p=0.008). The mutation correlated with a higher age at diagnosis (p=0.049) and with a greater tumor size (p=0.041). Multivariate analysis confirmed these findings. The prevalence of BRAFV600E mutation before 1986 was significantly lower than after it (p=0.008)., Conclusions: Our data suggest that BRAFV600E mutation is associated with high-risk clinicopathological characteristics of PTC and worse prognosis of patients. The frequency of the mutation significantly varied during the observed period but rather because of the different age distribution of patients in particular periods than as a consequence of Chernobyl accident.
- Published
- 2010
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6. HPV status and regional metastasis in the prognosis of oral and oropharyngeal cancer.
- Author
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Klozar J, Kratochvil V, Salakova M, Smahelova J, Vesela E, Hamsikova E, Betka J, and Tachezy R
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- Alphapapillomavirus genetics, Czech Republic epidemiology, DNA, Viral chemistry, Female, Human papillomavirus 16 genetics, Human papillomavirus 16 isolation & purification, Humans, Lymphatic Metastasis, Male, Middle Aged, Mouth Neoplasms pathology, Oropharyngeal Neoplasms pathology, Polymerase Chain Reaction, Prognosis, Risk Factors, Survival Analysis, Alphapapillomavirus isolation & purification, Mouth Neoplasms mortality, Mouth Neoplasms virology, Oropharyngeal Neoplasms mortality, Oropharyngeal Neoplasms virology
- Abstract
Prognostic factors are important for treatment decisions as they help adapt the therapy on a case-to-case basis. Nodal status, number of positive nodes, and presence of extracapsular spread are considered to be the important prognostic factors in head and neck cancer. Some studies suggest that human papillomavirus (HPV) status also influences the outcome of the treatment. This influence can be explained by the variation in tendency to develop regional metastases and by variation in the type of neck node involvement. The study objectives were to compare patients with HPV positive and HPV-negative tumors for survival and prevalence and type of regional metastasis, to identify prognostic factors and to test whether HPV presence is an independent factor of survival. The study included 81 patients treated by surgery including neck dissection for oral or oropharyngeal squamous cell cancer. A computerized medical report was completed for each patient. Analysis of the tumor specimen for the HPV DNA presence was done on paraffin-fixed tissue. HPV DNA detection and typing were performed by PCR with GP5+/GP6+BIO primers and reverse line blot hybridization. Overall, 64% (52/81) of tumors were HPV positive with 80% in the tonsillar site. HPV-positive patients had significantly better both overall (73 vs. 35%) (P=0.0112) and disease-specific (79 vs. 45%) (P=0.0015) survival rates than HPV-negative patients. No significant differences were found in the pN classification, in the number of positive nodes and the presence of extracapsular spread in the involved nodes between HPV positive and HPV-negative tumors. Multivariate analysis showed that significant prognostic factors of survival were the presence of HPV in the tumor, extracapsular spread and tumor size. HPV was the most significant prognostic factor in the studied group of patients with oropharyngeal tumors (HR=0.27, 95%CI 0.12-0.61) and possibly should be considered in treatment decisions.
- Published
- 2008
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7. Management of benign stenoses of the large airways in the university hospital in Prague, Czech Republic, in 1998-2003.
- Author
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Marel M, Pekarek Z, Spasova I, Pafko P, Schutzner J, Betka J, and Pospisil R
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- Adolescent, Adult, Aged, Bronchial Diseases epidemiology, Bronchial Diseases etiology, Bronchial Diseases therapy, Bronchoscopy methods, Constriction, Pathologic epidemiology, Constriction, Pathologic etiology, Constriction, Pathologic therapy, Czech Republic epidemiology, Female, Hospitals, University, Humans, Intubation, Intratracheal adverse effects, Male, Middle Aged, Prospective Studies, Tracheal Stenosis epidemiology, Tracheal Stenosis etiology, Tracheostomy adverse effects, Tracheal Stenosis therapy
- Abstract
Background: Clinically significant benign stenoses of the large airways develop in about 1% of patients after intubation. The management of benign stenoses is not unified around the world, nor are there any accepted methods for their screening., Objectives: The purpose of this study is to describe and compare results of interventional bronchoscopy and surgical therapy of benign stenoses as well as to propose an algorithm for the management of this airways disorder., Methods: Prospective study on 80 consecutive patients with benign stenoses of the large airways admitted to the Pulmonary Department of the University Hospital of Prague-Motol., Results: Sixty-two patients developed stenoses after endotracheal intubation or tracheostomy, in 18 patients the stenosis was caused by other diseases or pathological situations. Thirty-eight patients were sent for surgical resection of the stenotic part of the airways. 2 surgically treated patients developed recurrence of the stenosis and had to be reoperated on. Narrowing of the trachea at the site of end-to-end anastomosis developed in 6 other patients and was cured by interventional bronchoscopy. The remaining 42 patients were treated by interventional bronchoscopy (Nd-YAG laser, electrocautery, stent) which was curative in 35 patients. Sixty-five patients were alive at the time of evaluation, 15 patients died. Five of them died between 3 and 14 (median 4) months after surgery from a disease other than airway stenosis. Ten nonresected patients also died, with 1 exception, due to a disease other than airway stenosis; the median survival was 9 months., Conclusions: We recommend to assess the patient for surgery after the initial diagnosis and therapeutic bronchoscopy with dilatation of the stenosis. If the patient is not a suitable candidate for resection, interventional bronchoscopy is an appropriate alternative for the management of benign stenoses of the large airways., (Copyright (c) 2005 S. Karger AG, Basel.)
- Published
- 2005
- Full Text
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8. On the beginnings of otorhinolaryngology (ORL) in Bohemia and Moravia.
- Author
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Skerík P and Betka J
- Subjects
- Czech Republic, History, 19th Century, History, 20th Century, Otorhinolaryngologic Surgical Procedures history, Publications history, Societies, Medical history, Otolaryngology history
- Published
- 2005
- Full Text
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9. First auditory brainstem implant in the Czech Republic.
- Author
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Zvĕrina E, Sollmann WP, Betka J, Skrivan J, Tichý T, Nevison B, and Urgosík D
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- Adult, Czech Republic, Evoked Potentials, Auditory, Brain Stem, Female, Hearing Loss, Central complications, Humans, Lipreading, Neurofibromatosis 2 complications, Treatment Outcome, Brain Stem surgery, Cochlear Nucleus, Hearing Loss, Central surgery, Neurofibromatosis 2 surgery, Prosthesis Implantation
- Abstract
In the Czech Republic, the first implantation of a stimulation electrode into the brainstem was performed on 11 January 1999 in the Department of ORL, Head and Neck Surgery, The First Medical Faculty, Charles University in Prague, University Hospital Motol. The selected patient was a 40-year-old woman with neurofibromatosis type 2 (NF2) who had previously undergone bilateral vestibular schwannoma surgery. Both tumours had been radically removed, the left-sided tumour in 1987, the right-sided one in 1988. She had been completely deaf since the last operation, i.e., for 11 years. The surgery was realized by the international cooperation of three teams. Placement of the electrode pad of the Nucleus CI21 + 1M system on the ventral and dorsal cochlear nuclei was performed. Electrically evoked auditory brainstem responses (EABRs) proved the correct position of the electrode array. The post-operative course was uneventful. Six weeks after the surgery the patient received her speech processor. Since that time, the patient already absolved several sessions of a speech processor tune-up. She uses the device as an aid in lip-reading. No adverse or pathological side effects have been observed. The patient was the 45th person in Europe to receive an ABI and the first in the Czech Republic.
- Published
- 2000
- Full Text
- View/download PDF
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