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1.
Khirurgiia (Mosk) ; (8): 5-11, 2022.
Artigo em Russo | MEDLINE | ID: mdl-35920217

RESUMO

BACKGROUND: Endoscopic submucosal dissection (ESD) is a perspective method of organ-sparing treatment of benign colon tumors. MATERIAL AND METHODS: The study included 1.000 patients with colon neoplasms who underwent ESD between October 2016 and October 2021. All surgeries were performed under intravenous sedation. RESULTS: Mean dimension of tumors was 3.4 cm, median of surgery time - 51 (31; 101) minutes. Conversion of endoscopic approach occurred in 7.6% of cases. The main cause of conversion was unsatisfactory lifting in submucosal injection process. Incidence of en bloc and R0 resections was 84.1% and 68.3%, respectively. Postoperative morbidity was 2.9% that correlates with the world literature data. CONCLUSION: Endoscopic submucosal dissection is an effective and safe method for benign colon neoplasms. Considering high incidence of en bloc resection and low rate of local recurrence in benign neoplasms, further research of efficacy and safety of ESD in early colon cancer is needed.


Assuntos
Neoplasias do Colo , Ressecção Endoscópica de Mucosa , Neoplasias do Colo/patologia , Neoplasias do Colo/cirurgia , Dissecação/efeitos adversos , Dissecação/métodos , Ressecção Endoscópica de Mucosa/efeitos adversos , Ressecção Endoscópica de Mucosa/métodos , Humanos , Duração da Cirurgia , Estudos Retrospectivos , Resultado do Tratamento
2.
Vopr Onkol ; 62(1): 112-16, 2016.
Artigo em Russo | MEDLINE | ID: mdl-30444588

RESUMO

Peutz-Jeghers syndrome is a rare hereditary syndrome characterized by presence of hamartoma polyps in intestinal tract and usually by mucocutaneous pigmentation. Clinical-genetic characteristics of Russian patients with Peutz-Jeghers syndrome were studied for the first time. Four germline mutations in STK11gene were found in probands from six families and three of them had not been described previously. Clinical pattern of disease in Russian patients included: frequent polyposis of colon and stomach (62,5% and 75%, respectively) along with small bowel; frequent presence of malignant tumors (62,5%). These clinical aspects can help physicians to find out Peutz-Jeghers syndrome. Molecular-genetic testing of individuals should be recommended.


Assuntos
Mutação em Linhagem Germinativa , Proteínas de Neoplasias/genética , Síndrome de Peutz-Jeghers/genética , Proteínas Serina-Treonina Quinases/genética , Quinases Proteína-Quinases Ativadas por AMP , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Proteínas de Neoplasias/metabolismo , Síndrome de Peutz-Jeghers/enzimologia , Síndrome de Peutz-Jeghers/patologia , Projetos Piloto , Proteínas Serina-Treonina Quinases/metabolismo
3.
Vestn Ross Akad Med Nauk ; 71(4): 3223-31, 2016.
Artigo em Russo | MEDLINE | ID: mdl-29297651

RESUMO

Aim: Transanal endoscopic microsurgery (TEM) is a main treatment technique for rectal adenomas, but can also be used for selected malignant tumors. This study presents TEM experience. Methods: The study enrolled patients with rectal adenomas, and selected adenocarcinomas. Preoperative work-up included: digital rectal examination, rectoscopy with biopsy, colonoscopy, EUS, pelvic MRI. Results: Three hundred and thirty patients [mean age of 61,4±10 (33­88)] underwent TEM. The mean size ± SD of tumors was 3.2±1.2 cm (0.6­10.0). Mean distance from anal verge was 6.7±2.6 cm (2.0­14.0). Preoperative biopsy revealed: adenoma ­ 263/330 (79,7%), adenocarcinoma ­ 67/330 (20,3%). The median operating time was 40 (15­220) min. Tumor-free margins were obtained in all operative specimens. In 5/330 (1.5%) cases tumors were fragmented. The morbidity rate was 19/330 (5.7%). Pathological investigation revealed: adenoma in 192/330 (58.1%) cases, adenocarcinoma stage Tis, T1, T2 and T3 in 138/330 (41.9%). Median follow-up lasted for 24 (1­57) months. Five patients (2.0%) with adenoma and four patients (5.2%) with adenocarcinoma had local recurrence. Conclusion: Transanal endoscopic microsurgery for rectal adenomas and selected malignant tumors is associated with low morbidity and low recurrents rates.


Assuntos
Adenocarcinoma , Adenoma , Complicações Pós-Operatórias , Neoplasias Retais , Microcirurgia Endoscópica Transanal , Adenocarcinoma/diagnóstico , Adenocarcinoma/patologia , Adenocarcinoma/cirurgia , Adenoma/diagnóstico , Adenoma/patologia , Adenoma/cirurgia , Adulto , Idoso , Idoso de 80 Anos ou mais , Biópsia/estatística & dados numéricos , Humanos , Margens de Excisão , Pessoa de Meia-Idade , Recidiva Local de Neoplasia/epidemiologia , Recidiva Local de Neoplasia/patologia , Estadiamento de Neoplasias , Duração da Cirurgia , Complicações Pós-Operatórias/diagnóstico , Complicações Pós-Operatórias/epidemiologia , Prognóstico , Neoplasias Retais/diagnóstico , Neoplasias Retais/patologia , Neoplasias Retais/cirurgia , Federação Russa/epidemiologia , Microcirurgia Endoscópica Transanal/efeitos adversos , Microcirurgia Endoscópica Transanal/métodos , Resultado do Tratamento
4.
Vopr Onkol ; 61(6): 998-1005, 2015.
Artigo em Russo | MEDLINE | ID: mdl-26995995

RESUMO

Transanal endoscopic microsurgery (TEM/TEO) is a standard treatment for rectal adenomas but can also be used for selected malignant tumors. Rectal adenomas, selected adenocarcinomas and carcinoids were chosen for operations. Preoperative work-up included: digital rectal examination, rectoscopy with biopsy, colonoscopy, EUS, pelvic CT (MRI). Two hundred and two patients [mean age of 62.4 ± 10.3 (33-86)] had TEO. The mean size ± SD of tumors was 3.2 ± 1.4 cm (0.6-8.0). Mean distance from anal verge and dental line was 7.1 ± 2.4 cm (2.5-14.0) and 4.6 ± 2.6 cm (0.5-12.0), respectively. Preoperative biopsy revealed: adenoma--156/202 (77.2%), adenocarcinoma--39/202 (19.3%) and carcinoid--7/202 (3.5%). The median operating time was 40 (20-180) min. Tumor-free margins were obtained in 200/202 (99%) operative specimens, 2/202 (1.0%) cases tumors were fragmented. Morbidity was 7/202 (3.5%). Pathological investigation revealed: adenoma in 109/202 (54.0%) cases, adenocarcinoma stage Tis, T1, T2 and T3 in 86/202 (42.5%), carcinoid in 5/202 (2.5%), neurilemoma in 1/202 (0.5%), neurofibroma in 1/202 (0.5%). One hundred and two patients had follow-up (95%). Median follow-up at 20 (1-41) months; 3/192 patients with adenocarcinoma, 1/192 patient with adenoma and 1/192 patient with carcinoid had local recurrence. Thus, transanal endoscopic microsurgery for rectal adenomas and selected malignant tumors is associated with low morbidity and low recurrents rates.


Assuntos
Neoplasias Retais/cirurgia , Microcirurgia Endoscópica Transanal , Adenocarcinoma/cirurgia , Adenoma/cirurgia , Adulto , Idoso , Tumor Carcinoide/cirurgia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Recidiva Local de Neoplasia/cirurgia , Neurofibroma/cirurgia , Duração da Cirurgia , Lesões Pré-Cancerosas/cirurgia , Neoplasias Retais/diagnóstico , Resultado do Tratamento
5.
Bull Exp Biol Med ; 158(1): 80-3, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25403403

RESUMO

Flow cytometry measurement of the expression of surface marker CD133 simultaneously with the analysis of fluorescent dye exclusion was performed in order to develop new methods for detection of cancer stem cell populations in tumor tissue samples from patients with colorectal adenocarcinoma. No correlation was found between the count of CD133(+) cancer cells and the volume of the "population" formed from cells actively pumping off the fluorescent dye. On the other hand, the fluorescence distribution plot showed predominant location of CD133(+) cancer cells among cells stained with neither DyeCycle Violet DNA-binding dye, nor rhodamine 123 mitochondrial dye. These cells did not show the properties of the classical "side population", because they did not shift to the area of stained cell after treatment with ionic channel blocker verapamil.


Assuntos
Transportadores de Cassetes de Ligação de ATP/metabolismo , Adenocarcinoma/metabolismo , Antígenos CD/metabolismo , Neoplasias Colorretais/metabolismo , Corantes Fluorescentes/metabolismo , Glicoproteínas/metabolismo , Peptídeos/metabolismo , Antígeno AC133 , Adenocarcinoma/patologia , Biomarcadores Tumorais/metabolismo , Neoplasias Colorretais/patologia , Humanos , Células-Tronco Neoplásicas/metabolismo , Rodamina 123/metabolismo , Coloração e Rotulagem
6.
Colorectal Dis ; 16(5): O182-5, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24330465

RESUMO

AIM: This publication will describe our own experience of using the ERBEJET2(®) water-jet dissector during surgical interventions for rectal cancer. METHOD: We utilized the water-jet dissection technique to obtain tissue specimens in 10 patients with rectal cancer. All patients thus underwent nerve-sparing low anterior resection of the rectum along with para-aortic lymphadenectomy. No intraoperative complications were registered. The postoperative period went uncomplicated in all patients. No dysuria was observed. Obtained tissue specimens were examined morphologically. Macroscopic examination included assessments of the preservation of the rectal fascia propria and the amount of cellular tissue along the anterior, posterior, and lateral surfaces of the rectum. We performed microscopy of the circumferential resection margin to characterize the surgical clearance and the intensity and depth of damage to the mesorectal tissue. On morphological examination, the quality of mesorectal excision was found to be good (Grade 3) in all 10 patients. RESULTS: As the results of our study demonstrate, the depth of lateral tissue damage is minimal with the water-jet dissector. CONCLUSION: Water-jet dissectors have their own place in the long list of armamentarium used in surgical interventions performed for rectal cancer and contribute to improving oncological and functional outcomes of surgical treatment in this patient population.


Assuntos
Dissecação/instrumentação , Excisão de Linfonodo , Neoplasias Retais/patologia , Neoplasias Retais/cirurgia , Idoso , Aorta , Perda Sanguínea Cirúrgica , Dissecação/efeitos adversos , Dissecação/métodos , Fáscia/lesões , Feminino , Humanos , Tempo de Internação , Masculino , Pessoa de Meia-Idade , Neoplasia Residual , Duração da Cirurgia , Reto/lesões
7.
Bull Exp Biol Med ; 152(6): 739-42, 2012 Apr.
Artigo em Inglês, Russo | MEDLINE | ID: mdl-22803178

RESUMO

Co-expression of colorectal adenocarcinoma cancer stem cells marker CD133 and a set of surface molecules described in published reports as possible cancer stem cell markers of other solid tumors was analyzed by flow cytometry. Minor cell populations expressing CD29, CD34, CD90, and CD117 against the background of CD133 expression were detected in cancer cells suspensions from the patients with colorectal adenocarcinoma. Our findings suggest that these markers can be used as additional markers of cancer stem cells of human colorectal adenocarcinoma.


Assuntos
Adenocarcinoma/genética , Antígenos CD/genética , Biomarcadores Tumorais/genética , Neoplasias Colorretais/genética , Células-Tronco Neoplásicas/metabolismo , Adenocarcinoma/imunologia , Adenocarcinoma/patologia , Antígenos CD/imunologia , Biomarcadores Tumorais/imunologia , Biópsia , Neoplasias Colorretais/imunologia , Neoplasias Colorretais/patologia , Citometria de Fluxo , Expressão Gênica , Humanos , Células-Tronco Neoplásicas/imunologia , Células-Tronco Neoplásicas/patologia
8.
Bull Exp Biol Med ; 151(2): 234-8, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-22238758

RESUMO

The expression of puitative surface molecular markers of cancer stem cells on human colorectal adenocarcinoma cells was analyzed by flow cytofluorometry. Cell subpopulations expressing markers of epithelial and malignant cells and stem cell markers were identified. Four minor subpopulations with CD24(+)/CD133(+), CD44(+)/CD133(+), CD90(+)/CD71(+), or CD90(+)/CD24(+) phenotypes meeting this requirement were detected; presumably, those were cancer stem cell subpopulations. These results extend our knowledge on heterogeneity of human colorectal adenocarcinoma cell population and outline new trends of research of cancer stem cell phenotype in these tumors.


Assuntos
Adenocarcinoma/patologia , Antígenos CD/metabolismo , Antígenos de Neoplasias/metabolismo , Biomarcadores Tumorais/metabolismo , Moléculas de Adesão Celular/metabolismo , Neoplasias Colorretais/patologia , Células-Tronco Neoplásicas/metabolismo , Adenocarcinoma/metabolismo , Neoplasias Colorretais/metabolismo , Molécula de Adesão da Célula Epitelial , Citometria de Fluxo , Humanos
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