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  1. AU="Kuznetsov, N S"
  2. AU=Rimmer Abi AU=Rimmer Abi
  3. AU="Zhou, Qinyao"
  4. AU="Taniguchi, Ryou"
  5. AU="Krauss, Thomas F"
  6. AU="Papoulidis, Ioannis"
  7. AU="Migaud, Henri"
  8. AU="Kelion, Andrew"
  9. AU="Harry Jabs"
  10. AU="Patel, Yatindra"
  11. AU="Aziza Jamal-Allial"
  12. AU="Montiel, Olga Martha"
  13. AU="Pérez Latorre, Leire"
  14. AU=Vardhan Seshu
  15. AU="OJ Baker"
  16. AU="Dalton, R C"
  17. AU="Mrozikiewicz-Rakowska, Beata"
  18. AU="Penkert, Judith"
  19. AU="Mak, Susanna"
  20. AU="Karkoszka, Henryk"
  21. AU="Burton, Jeffrey H"
  22. AU="Frederique Pitel"
  23. AU="Pierce, Aimee"
  24. AU="Luque-Ballesteros, Laura"
  25. AU="Dondi, Francesco"
  26. AU="McLachlan, Alex"
  27. AU="Krizova, Ludmila"
  28. AU="Balog, Attila"
  29. AU="Faerber, Karin"
  30. AU="Prettner, Klaus"
  31. AU="Ambrožová, I."
  32. AU="William, Doreen"
  33. AU="Gutiérrez-Sánchez, A M"
  34. AU="Bohan, Dana"
  35. AU="Spracklen, D."
  36. AU="Lobo, Brian C"
  37. AU=Zhuang Jianjian AU=Zhuang Jianjian
  38. AU=Pathanki Adithya M
  39. AU="Armando Vilchis-Ordoñez"
  40. AU="Zhongfu Lu"
  41. AU="Lo, Hong-Yip"
  42. AU="Ziman Xiong"
  43. AU="Oakes, Allison H"
  44. AU="Ma, Shaotong"
  45. AU="Zang, Lili"
  46. AU="Adams Brian D"
  47. AU="Maria Papaioannou"
  48. AU="Kollia, Georgia"
  49. AU="Auxiette, Catherine"
  50. AU="Guzmán, Luis"
  51. AU="Alipour, Elnaz"
  52. AU="Queiroz, Dayanna Joyce Marques"
  53. AU="Ramamurthy, Santosh"
  54. AU="Xueying Huang"
  55. AU="Cromwell, Howard C"
  56. AU="Spence, John C H"
  57. AU="Chapinal, Libertad"
  58. AU=Rohaim Mohammed A AU=Rohaim Mohammed A
  59. AU=Hempel Cornelius

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  1. Artikel: Sovremennye aspekty, vliyayushchie na taktiku vedeniya patsientov s papillyarnym rakom shchitovidnoi zhelezy.

    Skibitskaya, M V / Kuznetsov, N S

    Khirurgiia

    2023  , Heft 12, Seite(n) 89–94

    Abstract: Thyroid cancer (TC) is the most common malignant tumor of the endocrine glands and accounts to 3% of the total structure of oncological morbidity. Papillary thyroid cancer (PTC) is the most common histological variant of thyroid malignancies. It accounts ...

    Titelübersetzung Modern aspects influencing the management of patients with papillary thyroid cancer.
    Abstract Thyroid cancer (TC) is the most common malignant tumor of the endocrine glands and accounts to 3% of the total structure of oncological morbidity. Papillary thyroid cancer (PTC) is the most common histological variant of thyroid malignancies. It accounts for about 85% of all cases of thyroid cancer. Despite good postoperative results and excellent survival compared to many other malignancies, tumor metastases to the paratracheal lymph nodes are quite common. This review of the literature considers the current personalized approach to patients with papillary thyroid cancer and current aspects influencing the management of patients with PTC.
    Mesh-Begriff(e) Humans ; Thyroid Cancer, Papillary/diagnosis ; Thyroid Cancer, Papillary/surgery ; Carcinoma, Papillary/diagnosis ; Carcinoma, Papillary/surgery ; Proto-Oncogene Proteins B-raf/genetics ; Thyroid Neoplasms/diagnosis ; Thyroid Neoplasms/surgery ; Thyroid Neoplasms/pathology ; Lymph Nodes/pathology ; Mutation
    Chemische Substanzen Proto-Oncogene Proteins B-raf (EC 2.7.11.1)
    Sprache Russisch
    Erscheinungsdatum 2023-12-13
    Erscheinungsland Russia (Federation)
    Dokumenttyp Review ; English Abstract ; Journal Article
    ZDB-ID 419230-8
    ISSN 2309-5628 ; 0023-1207
    ISSN (online) 2309-5628
    ISSN 0023-1207
    DOI 10.17116/hirurgia202312189
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  2. Artikel: Effektivnost' preparata Meksidol v korrektsii postkovidnogo sindroma u patsientov s khronicheskimi tserebrovaskulyarnymi zabolevaniyami.

    Kuznetsova, E B / Salina, E A / Kuznetsov, N S

    Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

    2023  Band 123, Heft 5, Seite(n) 117–122

    Abstract: Objective: To evaluate the effectiveness of sequential therapy with Mexidol and Mexidol FORTE 250 in the correction of postcovoid syndrome (PKS) in patients with chronic cerebrovascular diseases (CVD).: Material and methods: The analysis of the ... ...

    Titelübersetzung Efficacy of Mexidol in the correction of postcovid syndrome in patients with chronic cerebrovascular diseases.
    Abstract Objective: To evaluate the effectiveness of sequential therapy with Mexidol and Mexidol FORTE 250 in the correction of postcovoid syndrome (PKS) in patients with chronic cerebrovascular diseases (CVD).
    Material and methods: The analysis of the results of examination and treatment of 110 patients with CVD who underwent COVID-19 was carried out. Patients of the main group (OH,
    Results: There was a significant improvement in the state of cognitive functions, regression of symptoms of asthenia, improvement of night sleep in patients with OG. The differences were statistically significant both in comparison with the baseline level and the HS.
    Conclusion: The administration of the drug does not require age-related dose adjustment and is well combined with basic therapy. The recommended regimen for the use of Mexidol: 14 days of 5 ml i/v or i/m, then taking the drug Mexidol FORTE 250 at a dose of 1 table 3 times/day for 2 months.
    Mesh-Begriff(e) Humans ; COVID-19/complications ; Antioxidants ; Asthenia ; Cerebrovascular Disorders/complications ; Cerebrovascular Disorders/drug therapy ; Chronic Disease ; Syndrome
    Chemische Substanzen emoxypine succinate (2R985002CT) ; Antioxidants
    Sprache Russisch
    Erscheinungsdatum 2023-06-14
    Erscheinungsland Russia (Federation)
    Dokumenttyp English Abstract ; Journal Article
    ZDB-ID 1201462-x
    ISSN 2309-4729 ; 1997-7298 ; 0044-4588
    ISSN (online) 2309-4729
    ISSN 1997-7298 ; 0044-4588
    DOI 10.17116/jnevro2023123051117
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  3. Artikel ; Online: Spin Noise in Birefringent Media.

    Kozlov, V O / Kuznetsov, N S / Smirnov, D S / Ryzhov, I I / Kozlov, G G / Zapasskii, V S

    Physical review letters

    2022  Band 129, Heft 7, Seite(n) 77401

    Abstract: It is known that linear birefringence of the medium essentially hinders measuring the Faraday effect. For this reason, optically anisotropic materials have never been considered as objects of the Faraday-rotation-based spin noise spectroscopy. We show, ... ...

    Abstract It is known that linear birefringence of the medium essentially hinders measuring the Faraday effect. For this reason, optically anisotropic materials have never been considered as objects of the Faraday-rotation-based spin noise spectroscopy. We show, both theoretically and experimentally, that strong optical anisotropy that may badly suppress the regular Faraday rotation of the medium, practically does not affect the measurement of the spatially uncorrelated spin fluctuations. We also show that the birefringent media provide additional opportunity to measure spatial spin correlations. Results of the experimental measurements of the spin-noise spectra performed on Nd^{3+} ions in the uniaxial crystal matrices well agree with the theory.
    Sprache Englisch
    Erscheinungsdatum 2022-08-26
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 208853-8
    ISSN 1079-7114 ; 0031-9007
    ISSN (online) 1079-7114
    ISSN 0031-9007
    DOI 10.1103/PhysRevLett.129.077401
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  4. Artikel: Enukleatsiya opukholei podzheludochnoi zhelezy (mnogotsentrovoe issledovanie).

    Solodkiy, V A / Kriger, A G / Akhaladze, G G / Goev, A A / Goncharov, S V / Gorin, D S / Zagainov, V E / Kuznetsov, N S / Kuchin, D M / Latkina, N V / Lysanyuk, M V / Maistrenko, N A / Martirosyan, T A / Romashchenko, P N / Shuinova, E A / Yukina, M Yu

    Khirurgiia

    2023  , Heft 2, Seite(n) 13–20

    Abstract: Objective: To evaluate the immediate results of enucleation of pancreatic neuroendocrine tumors (pNETs).: Material and methods: The results of enucleation of pancreatic neuroendocrine tumors (pNETs) were analyzed in 95 patients between 2016 and 2021. ...

    Titelübersetzung Enucleation of pancreatic tumors: a multiple-center study.
    Abstract Objective: To evaluate the immediate results of enucleation of pancreatic neuroendocrine tumors (pNETs).
    Material and methods: The results of enucleation of pancreatic neuroendocrine tumors (pNETs) were analyzed in 95 patients between 2016 and 2021. Functioning tumors (mean size 16.8 mm) were found in 70 patients, non-functioning (mean size 25 mm) - in 25 patients. Intraparenchymal tumors were found in 48 people, extraorganic lesion - in 47 patients.
    Results: There were 262 patients with pNETs who underwent various surgeries between 2016 and 2021. Various resections were performed in 167 (63.8%) cases, enucleations - in 95 (36.2%) patients. Traditional surgical approach was used in 65 patients. Pancreatic fistula occurred in 21 patients (type B - 17, type C - 4), while arrosive bleeding occurred in 6 patients with unfavorable outcomes in 2 cases. Minimally invasive surgeries were performed in 30 patients. Eight patients with intraparenchymal tumors required conversion to open surgery. Type B pancreatic fistula occurred in 5 patients that led to arrosive bleeding in 2 cases (hemostasis was provided by endovascular method). Comparison of intraparenchymal and extraorgan tumors regarding the incidence of pancreatic fistula revealed odds ratio 5.26 (95% CI 1.5355; 18.0323,
    Conclusion: Enucleation is advisable for highly differentiated pancreatic neuroendocrine tumors up to 2 cm. Minimally invasive enucleation is indicated for extraorgan tumors. Intraparenchymal tumors significantly increase the risk of postoperative complications.
    Mesh-Begriff(e) Humans ; Pancreatectomy/adverse effects ; Pancreatectomy/methods ; Pancreatic Fistula/epidemiology ; Pancreatic Fistula/etiology ; Pancreatic Fistula/surgery ; Neuroendocrine Tumors/complications ; Treatment Outcome ; Retrospective Studies ; Pancreatic Neoplasms/pathology ; Postoperative Complications/epidemiology ; Postoperative Complications/etiology ; Postoperative Complications/surgery ; Neuroectodermal Tumors, Primitive/complications ; Neuroectodermal Tumors, Primitive/surgery
    Sprache Russisch
    Erscheinungsdatum 2023-02-02
    Erscheinungsland Russia (Federation)
    Dokumenttyp Multicenter Study ; English Abstract ; Journal Article
    ZDB-ID 419230-8
    ISSN 2309-5628 ; 0023-1207
    ISSN (online) 2309-5628
    ISSN 0023-1207
    DOI 10.17116/hirurgia202302113
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  5. Artikel ; Online: [Survival predictors in patients with ectopic acth syndrome].

    Golounina, O O / Belaya, Zh/ E / Rozhinskaya, L Ya / Pikunov, M Yu / Markovich, A A / Dzeranova, L K / Marova, E I / Kuznetsov, N S / Fadeev, V V / Melnichenko, G A / Dedov, I I

    Problemy endokrinologii

    2022  Band 68, Heft 6, Seite(n) 30–42

    Abstract: Aim: To determine significant factors affecting the survival of patients with ectopic ACTH syndrome (EAS).: Materials and methods: A multi-center, observational study with a retrospective analysis of patients with EAS. The end point of the study was ... ...

    Abstract Aim: To determine significant factors affecting the survival of patients with ectopic ACTH syndrome (EAS).
    Materials and methods: A multi-center, observational study with a retrospective analysis of patients with EAS. The end point of the study was the fatal outcome of patients from various causes. In order to identify predictors of survival or mortality, univariate and multifactorial Cox regression analyses were carried out. ROC-analysis was used to determine the prognostic threshold values of individual predictors. The survival analysis was carried out using the Kaplan-Mayer method. Statistical data processing was carried out by using IBM SPSS Statistics 23.
    Results: The age of patients at the time of diagnosis ranged from 12 to 76 years (Me 40 years [28;54]). The age of the studied population was 55 years [38; 64] for women and 42 years [32; 54] for men. The median period of observation was 50 months [13;91], with a maximum follow-up of 382 months. 92 patients (60,9%) had bronchopulmonary NET, 17 (11,3%) - thymic carcinoid, 8 - pancreatic NET, 5 -pheochromocytoma, 1- cecum NET, 1- appendix carcinoid tumor, 1 - medullary thyroid cancer and 26 (17,2%) patients had an occult NET. The primary tumor was removed in 101 patients (66,9%). Bilateral adrenalectomy was performed in 42 (27,8%) cases. Metastases were revealed in 23,2% (n=35) of patients. Relapse of the disease was observed in 24,4%, long-term remission was preserved in 64 patients (74,4%). Death occurred in 42 patients (28%). The average age of survivors was 47,0±15,2 versus 53,5±15,6 years for the deceased (p=0,022). The average survival time from diagnosis for the deceased was 32 months, Me 16,5 months [7;54]. Multivariate analysis revealed that the following factors have a direct impact on survival: age of diagnosis ≥51 years (OR 4,493; 95% CI 2,056-9,818, p<0,001), bronchopulmonary neuroendocrine tumor (NET) (OR 0,281; 95% CI 0,119-0,665, p=0,004), the presence of distant metastases (OR 2,489; 95% CI 1,141-5,427, p=0,022), late-night salivary cortisol (LNSC) ≥122,2 nmol/L (OR 2,493; 95% CI 1,014-6,128, p=0,047).
    Conclusion: The prognosis of patients with EAS is influenced by the age of diagnosis, NET localization, distant metastases and level of LNSC. The most common cause of ectopic ACTH syndrome was bronchopulmonary NET which was associated with the best survival rate.
    Mesh-Begriff(e) Male ; Humans ; Female ; Infant, Newborn ; Child ; Adolescent ; Young Adult ; Adult ; Middle Aged ; Aged ; ACTH Syndrome, Ectopic/diagnosis ; Retrospective Studies ; Carcinoid Tumor ; Neuroendocrine Tumors/diagnosis ; Adrenal Gland Neoplasms
    Sprache Russisch
    Erscheinungsdatum 2022-08-15
    Erscheinungsland Russia (Federation)
    Dokumenttyp Observational Study ; English Abstract ; Journal Article
    ZDB-ID 421785-8
    ISSN 2308-1430 ; 2072-6406 ; 0032-9509 ; 0375-9660
    ISSN (online) 2308-1430
    ISSN 2072-6406 ; 0032-9509 ; 0375-9660
    DOI 10.14341/probl13144
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  6. Artikel: Khirurgicheskoe lechenie AKTG-éktopicheskogo sindroma.

    Krylov, V V / Dobreva, E A / Kharnas, S S / Kuznetsov, N S / Marova, E I / Levkin, V V

    Khirurgiia

    2019  , Heft 8, Seite(n) 74–78

    Abstract: ACTH-ectopic syndrome is a severe, multiple-symptom disease characterized by secretion of adrenocorticotropic hormone (ACTH) by ectopic tumor, increased release of adrenal cortical hormones and clinical picture of hypercorticism. Diagnosis and treatment ... ...

    Titelübersetzung Surgical treatment of ACTH-ectopic syndrome.
    Abstract ACTH-ectopic syndrome is a severe, multiple-symptom disease characterized by secretion of adrenocorticotropic hormone (ACTH) by ectopic tumor, increased release of adrenal cortical hormones and clinical picture of hypercorticism. Diagnosis and treatment of ACTH-ectopic syndrome is still difficult problem despite the achievements of modern medicine. There are several unresolved issues including optimal diagnostic algorithm, indications for various surgical procedures and their optimal dates. This review is devoted to these questions.
    Mesh-Begriff(e) ACTH Syndrome, Ectopic/diagnosis ; ACTH Syndrome, Ectopic/etiology ; ACTH Syndrome, Ectopic/surgery ; Adrenocortical Hyperfunction/diagnosis ; Adrenocortical Hyperfunction/etiology ; Adrenocortical Hyperfunction/surgery ; Algorithms ; Humans
    Sprache Russisch
    Erscheinungsdatum 2019-09-26
    Erscheinungsland Russia (Federation)
    Dokumenttyp Journal Article ; Review
    ZDB-ID 419230-8
    ISSN 2309-5628 ; 0023-1207
    ISSN (online) 2309-5628
    ISSN 0023-1207
    DOI 10.17116/hirurgia201908174
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  7. Artikel: [Clinical and laboratory characteristics and results of treatment of patients with ACTH-producing neuroendocrine tumors of various localization].

    Golounina, O O / Belaya, Z E / Rozhinskaya, L Y / Marova, E I / Pikunov, M Y / Khandaeva, P M / Arapova, S D / Dzeranova, L K / Kuznetsov, N S / Fadeev, V V / Melnichenko, G A / Dedov, I I

    Terapevticheskii arkhiv

    2021  Band 93, Heft 10, Seite(n) 1171–1178

    Abstract: Aim: To study the clinical, biochemical characteristics, treatment results and follow-up of patients with ectopic ACTH syndrome EAS (ACTH adrenocorticotropic hormone ).: Materials and methods: A retrospective, observational, single-center study of ... ...

    Abstract Aim: To study the clinical, biochemical characteristics, treatment results and follow-up of patients with ectopic ACTH syndrome EAS (ACTH adrenocorticotropic hormone ).
    Materials and methods: A retrospective, observational, single-center study of 130 patients with EAS. Demographic information of patients, medical history, results of laboratory and instrumental investigations at the pre- and postoperative stages and follow-up of EAS were analyzed.
    Results: The mean age at the diagnosis ranged from 12 to 74 years (Me 40 years [28; 54]). The duration of the disease from the onset of symptoms to the verification of the diagnosis varied from 2 to 168 months (Me 17.5 months [7; 46]). Eighty-one (62,3%) patients had bronchopulmonary NET, 9 thymic carcinoid, 7 pancreatic NET, 5 pheochromocytoma, 1 cecum NET, 1 appendix carcinoid tumor, 1 medullary thyroid cancer and 25 (19.2%) had an occult source of ACTH. The median follow-up period of patients was 27 months [9.75; 61.0] with a maximum follow-up of 372 months. Currently, primary tumor was removed in 82 (63.1%) patients, bilateral adrenalectomy was performed in 23 (18%) patients, in 16 of them there was an occult source of ACTH-producing NET and in 7 patients in order to control hypercortisolism after non-successful surgical treatment. Regional and distant metastases were revealed in 25 (19.2%) patients. At the time of the last observation 59 (72%) patients were exhibited a full recovery, 12 (14.6%) had relapse of the disease and 26 (20%) died from multiple organ failure (n=18), pulmonary embolism (n=4), surgical complications (n=2), disseminated intravascular coagulation syndrome (n=1) or COVID-19 (n=1).
    Conclusion: In our cohort of patients bronchopulmonary NET are the most frequent cause of EAS (62.3%). Surgical treatment leads to remission of hypercortisolism in 72% cases; the proportion of relapse (14.6%) and fatal outcome (20%) remains frequent in EAS.
    Mesh-Begriff(e) Humans ; Child ; Adolescent ; Young Adult ; Adult ; Middle Aged ; Aged ; Neuroendocrine Tumors/diagnosis ; Neuroendocrine Tumors/surgery ; Cushing Syndrome/diagnosis ; Cushing Syndrome/etiology ; Retrospective Studies ; COVID-19 ; Neoplasm Recurrence, Local/complications ; Adrenocorticotropic Hormone
    Chemische Substanzen Adrenocorticotropic Hormone (9002-60-2)
    Sprache Russisch
    Erscheinungsdatum 2021-10-15
    Erscheinungsland Russia (Federation)
    Dokumenttyp English Abstract ; Journal Article
    ZDB-ID 40718-5
    ISSN 2309-5342 ; 0040-3660
    ISSN (online) 2309-5342
    ISSN 0040-3660
    DOI 10.26442/00403660.2021.10.201102
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.A 79: Hefte anzeigen Standort:
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  8. Artikel: [ACTH-producing tumors of the chest: features of clinical course, diagnosis and surgical treatment].

    Dobreva, E A / Krylov, V V / Kuznetsov, N S / Parshin, V V / Ippolitov, L I

    Khirurgiia

    2015  , Heft 8 Pt 2, Seite(n) 45–51

    Mesh-Begriff(e) Adrenocorticotropic Hormone/blood ; Biomarkers, Tumor/blood ; Diagnostic Imaging/methods ; Humans ; Thoracic Neoplasms/diagnosis ; Thoracic Neoplasms/secretion ; Thoracic Neoplasms/surgery ; Thoracoscopy/methods
    Chemische Substanzen Biomarkers, Tumor ; Adrenocorticotropic Hormone (9002-60-2)
    Sprache Russisch
    Erscheinungsdatum 2015
    Erscheinungsland Russia (Federation)
    Dokumenttyp Journal Article ; Review
    ZDB-ID 419230-8
    ISSN 2309-5628 ; 0023-1207
    ISSN (online) 2309-5628
    ISSN 0023-1207
    DOI 10.17116/hirurgia20158245-51
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel: [Bronchopulmonary ACTH-producing tumors].

    Pikunov, M Iu / Kuznetsov, N S / Latkina, N V / Dobreva, E A / Remizov, O V

    Khirurgiia

    2014  , Heft 5, Seite(n) 21–27

    Abstract: Neuroendocrine tumors have the ability to produce the hormones and vasoactive peptides. Excess of these hormones leads to different symptoms and syndromes because of organs' injuries. Detection of ACTH origin by using of modern diagnostic methods is not ... ...

    Abstract Neuroendocrine tumors have the ability to produce the hormones and vasoactive peptides. Excess of these hormones leads to different symptoms and syndromes because of organs' injuries. Detection of ACTH origin by using of modern diagnostic methods is not always possible. Lungs and bronchi are one of the most frequent localization of ACTH-producing tumors. It is considered that carcinoids with bronchopulmonary localization like a benign tumors in the clinical course. But at the same time carcinoid tends to metastasize, so timely diagnostics and treatment improve quality of life significant and increase the life expectancy of patients. The modern state of diagnostics and surgical treatment problem of ACTH-producing tumors with bronchopulmonary localization is presented in the article. It was described the brief historical background, clinical symptoms, instrumental and biochemical methods of diagnosis. The principles of surgical treatment are presented in the article.
    Mesh-Begriff(e) ACTH Syndrome, Ectopic/blood ; ACTH Syndrome, Ectopic/diagnosis ; ACTH Syndrome, Ectopic/etiology ; ACTH Syndrome, Ectopic/physiopathology ; ACTH Syndrome, Ectopic/surgery ; Adolescent ; Adrenocorticotropic Hormone/blood ; Adult ; Algorithms ; Bronchial Neoplasms/blood ; Bronchial Neoplasms/complications ; Bronchial Neoplasms/pathology ; Bronchial Neoplasms/surgery ; Dexamethasone ; Early Detection of Cancer ; Early Medical Intervention ; Female ; Humans ; Lung Neoplasms/blood ; Lung Neoplasms/complications ; Lung Neoplasms/pathology ; Lung Neoplasms/surgery ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Monitoring, Physiologic/methods ; Neuroendocrine Tumors/blood ; Neuroendocrine Tumors/complications ; Neuroendocrine Tumors/pathology ; Neuroendocrine Tumors/surgery ; Pneumonectomy/methods ; Pneumonectomy/psychology ; Prognosis ; Quality of Life ; Tomography, X-Ray Computed ; Treatment Outcome
    Chemische Substanzen Dexamethasone (7S5I7G3JQL) ; Adrenocorticotropic Hormone (9002-60-2)
    Sprache Russisch
    Erscheinungsdatum 2014
    Erscheinungsland Russia (Federation)
    Dokumenttyp English Abstract ; Journal Article
    ZDB-ID 419230-8
    ISSN 2309-5628 ; 0023-1207
    ISSN (online) 2309-5628
    ISSN 0023-1207
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel: [Is the localization of the tumor in intra-peritoneal part of the rectum contraindication to transanal endoscopic microsurgery].

    Shelygin, Iu A / Rybakov, E G / Chernyshov, S V / Kuznetsov, N S

    Vestnik khirurgii imeni I. I. Grekova

    2014  Band 173, Heft 4, Seite(n) 43–46

    Abstract: Transanal endoscopic microsurgery (TEM) is the method used in cases of benign tumors at the early stages of rectal cancer. The tumor localization in peritonized part of the rectum indicates a limiting level for removal of the neoplasm. TEM was performed ... ...

    Abstract Transanal endoscopic microsurgery (TEM) is the method used in cases of benign tumors at the early stages of rectal cancer. The tumor localization in peritonized part of the rectum indicates a limiting level for removal of the neoplasm. TEM was performed on 137 patients. The mean age was 63.8 ± 9.8 years and the number of women consisted of 65.7%. Neoplasms were located in the upper ampullar rectum and a potential possibility of connection with the peritoneal cavity was noted in 12 (8.7%) patients, but during TEM it was only in 5 cases. There wasn't any conversion to a peritoneal surgery. The wound closures were carried out from the side of the rectum lumen and all the operations were finished with the control laparoscopy and formation of sigmostoma. The stomas were closed in 3 patients on fifth- sixth weeks. A connection with the peritoneal cavity during TEM isn't critical event in the case of wound closure through surgical rectoscope and it doesn't lead to the conversion to radical operation.
    Mesh-Begriff(e) Adenocarcinoma/pathology ; Adenocarcinoma/surgery ; Aged ; Colon, Sigmoid/surgery ; Colostomy/methods ; Female ; Humans ; Laparoscopy/methods ; Male ; Middle Aged ; Moscow ; Natural Orifice Endoscopic Surgery/adverse effects ; Natural Orifice Endoscopic Surgery/methods ; Neoplasm Staging ; Peritoneum/pathology ; Postoperative Care/methods ; Postoperative Complications/prevention & control ; Proctoscopy/adverse effects ; Proctoscopy/methods ; Rectal Neoplasms/pathology ; Rectal Neoplasms/surgery ; Rectum/pathology ; Rectum/surgery ; Retrospective Studies ; Treatment Outcome
    Sprache Russisch
    Erscheinungsdatum 2014
    Erscheinungsland Russia (Federation)
    Dokumenttyp English Abstract ; Journal Article
    ZDB-ID 603433-0
    ISSN 0042-4625
    ISSN 0042-4625
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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