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2.
Biomech Model Mechanobiol ; 16(6): 1819-1832, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-28553679

RESUMEN

Proof-of-concept computational models were developed and applied as tools to gain insights into biomechanical interactions and variations of oxygen gradients of wounded tissue subject to negative pressure wound therapy (NPWT), following trans-femoral amputation. A macro-scale finite-element model of a lower limb was first developed based on computed tomography data, and distributions of maximum and minimum principal stress values we calculated for a region of interest (ROI). Then, the obtained results were applied iteratively as new sets of boundary conditions for a specific spatial position in a capillary sub-model. Data from coupled capillary stress and mass- diffusion sub-models were transferred to the macro-scale model to map the spatial changes of tissue oxygen gradients in the ROI. The -70 mmHg NPWT resulted in a dramatic change of a wound surface area and the greatest relative contraction was observed at -150 mmHg. Tissue lateral to the depth of the wound cavity revealed homogenous patterns of decrease in oxygenation area and the extent of such decrease was dependent on the distance from the wound surface. However, tissue lateral to the width of the wound demonstrated heterogeneous patterns of change, as evidenced by both gradual increase and decrease in the oxygenation area. The multiscale models developed in the current study showed a significant influence of NPWT on both macro-deformations and changes of tissue oxygenation. The patterns of changes depended on the depth of the tissue, the geometry of the wound, and also the location of tissue plane.


Asunto(s)
Amputación Quirúrgica , Simulación por Computador , Fémur/cirugía , Terapia de Presión Negativa para Heridas , Cicatrización de Heridas , Difusión , Fémur/efectos de los fármacos , Procesamiento de Imagen Asistido por Computador , Músculos/efectos de los fármacos , Músculos/patología , Oxígeno/farmacología , Soporte de Peso
8.
J Obstet Gynaecol ; 32(8): 790-4, 2012 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-23075358

RESUMEN

The aim of this study is to compare collection of sufficient material and diagnostic accuracy of Pipelle biopsy with curettage and hysterectomy. A total of 82 cases with indications for endometrial biopsy for any reason and in which endometrial biopsy was performed with dilatation and curettage (D&C) and Pipelle aspiration biopsy, and 66 cases in which an indication for hysterectomy was established for any reason were included in the study. Histopathological findings were examined in the following six groups: normal; endometrial polyps; hyperplasia without atypia; hyperplasia with atypia; atrophy; and insufficient material. Descriptive statistical methods and McNemar's test were used. When the histopathological compatibility between Pipelle and D&C was considered (n=82), a diagnosis that was different from that obtained by D&C was obtained in 22 of the 63 cases (34%), in whom normal endometrial histology was found with a Pipelle biopsy specimen. It was observed that only 1 of 13 cases of endometrial polyps was diagnosed with Pipelle biopsy. Insufficient material was obtained in six cases (7%) with Pipelle biopsies and three cases (4%) with D&C. While Pipelle biopsies and D&C have a nearly equal level of success in widespread endometrial lesions, Pipelle biopsies provide limited diagnostic accuracy in cases with focal pathologies.


Asunto(s)
Dilatación y Legrado Uterino , Endometrio/patología , Histerectomía , Legrado por Aspiración/instrumentación , Adulto , Anciano , Biopsia/instrumentación , Biopsia/métodos , Femenino , Humanos , Persona de Mediana Edad , Estudios Prospectivos
9.
Clin Exp Obstet Gynecol ; 38(1): 96-8, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21485739

RESUMEN

During pregnancy there are hemostatic changes that may result in a hypercoagulable state producing thrombotic consequences. This condition may be aggravated in women who are carriers of congenital thrombophilic factors. These factors may increase obstetric complications such as miscarriages, fetal growth restriction, placental abruption and preeclampsia. Trombophilic factors may also cause venous thromboembolism, which is the leading cause of maternal morbidity and mortality. We report a case of a 22-year-old woman with factor V Leiden mutation, whose pregnancy was complicated with deep venous thrombosis requiring placement of a vena cava filter.


Asunto(s)
Complicaciones Hematológicas del Embarazo/terapia , Trombofilia/terapia , Filtros de Vena Cava , Trombosis de la Vena/terapia , Factor V/genética , Femenino , Humanos , Recién Nacido , Masculino , Embarazo , Complicaciones Hematológicas del Embarazo/sangre , Complicaciones Hematológicas del Embarazo/genética , Trombofilia/genética , Trombosis de la Vena/sangre , Trombosis de la Vena/genética , Adulto Joven
10.
Clin Exp Obstet Gynecol ; 38(4): 347-50, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-22268272

RESUMEN

PURPOSE OF INVESTIGATION: To evaluate the prevalence and effects of inherited thrombophilia caused by factor V Leiden, prothrombin G20210A and methylenetetrahydrofolate reductase (MTHFR) C677T mutations in women with recurrent pregnancy loss. METHODS: A study group of 97 women with recurrent miscarriages and a control group of 71 healthy pregnant women were included in the study. Genotype analyses for factor V Leiden, prothrombin G20210A and MTHFR C677T polymorphisms were performed by real-time polymerase chain reaction (RT-PCR). RESULTS: The frequency of factor V Leiden, prothrombin G20210A and MTHFR C677T mutations were similar in both the study and control group. There were eight patients (8.2%) who had more than one gene mutation in the study group and one patient in the control group (1.4%). This difference was not statistically significant. Study group patients (n = 97) were compared in terms of the number of miscarriages and the abortion week, in addition to being a carrier of factor V Leiden and MTHFR C677T gene mutations. No statistically significant correlation was found between being a factor V Leiden and MTHFR C677T mutation carrier with either the number of miscarriages or the abortion week. CONCLUSION: Factor V Leiden, prothrombin G20210A and MTHFR C677T gene mutations are not individually related with recurrent pregnancy loss. However, combined gene mutation status may be associated with recurrent miscarriages.


Asunto(s)
Aborto Habitual , Trombofilia/genética , Adulto , Estudios de Casos y Controles , Factor V/genética , Femenino , Humanos , Metilenotetrahidrofolato Reductasa (NADPH2)/genética , Mutación , Embarazo , Protrombina/genética , Adulto Joven
11.
Clin Exp Obstet Gynecol ; 37(2): 112-4, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-21077499

RESUMEN

PURPOSE OF INVESTIGATION: The effects of tamoxifen on lipid peroxidation and oxidant-antioxidant balance in an animal model were studied. METHODS: Twelve female adult rats were divided into two groups and DMSO and tamoxifen dissolved in DMSO were administered. Tissues taken from the brain, liver and ovary of rats were dissected. MDA, nitrite, nitrate levels and plasma LDL oxidation in brain, ovary and liver tissues were measured and compared. RESULTS: Induced LDL MDA levels were significantly lower in the tamoxifen group (p = 0.009). MDA levels in the liver were significantly lower in the tamoxifen group whereas nitrite levels were found significantly higher (p < 0.05). Brain and ovarian tissues demonstrated no significant difference with respect to MDA, nitrite and nitrate levels. CONCLUSION: Tamoxifen has no negative effects on lipid peroxidation in an animal model.


Asunto(s)
Antineoplásicos Hormonales/farmacología , Peroxidación de Lípido/efectos de los fármacos , Nitratos/metabolismo , Nitritos/metabolismo , Tamoxifeno/farmacología , Animales , Encéfalo/metabolismo , Femenino , Lipoproteínas LDL/sangre , Hígado/metabolismo , Ovario/metabolismo , Ratas
12.
Eur J Gynaecol Oncol ; 31(4): 415-7, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-20882884

RESUMEN

PURPOSE OF INVESTIGATION: To evaluate the effects of tamoxifen on the endometrium of breast cancer patients by hysteroscopy and endometrial sampling. METHODS: Thirty-seven breast cancer patients using tamoxifen underwent hysteroscopy because of postmenopausal endometrial thickening or abnormal uterine bleeding. Hysteroscopic findings were compared with histopathology and ultrasonographic measurement of the endometrium. RESULTS: Nineteen women showed endometrial abnormalities (51%) out of 37 patients. Negative and positive predictive values for hysteroscopy in detecting endometrial abnormalities were 100% and 94%, respectively. CONCLUSION: Endometrial surveillance is an important part of gynecological follow-up in breast cancer patients using tamoxifen and the liberal use of hysteroscopy aids in the diagnosis of abnormal endometrium.


Asunto(s)
Neoplasias de la Mama/tratamiento farmacológico , Endometrio/efectos de los fármacos , Antagonistas de Estrógenos/efectos adversos , Histeroscopía , Tamoxifeno/efectos adversos , Adulto , Anciano , Neoplasias de la Mama/patología , Endometrio/patología , Femenino , Humanos , Persona de Mediana Edad , Estudios Retrospectivos
13.
Eur J Gynaecol Oncol ; 31(6): 627-31, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-21319504

RESUMEN

PURPOSE OF INVESTIGATION: To evaluate the immunohistochemical expressions of p16 and p53 in cervical intraepithelial neoplasia (CIN) and do a comparison with non-neoplastic cervical lesions. METHODS: Sixty cases diagnosed as CIN after histopathological examination and 25 controls diagnosed as chronic cervicitis were included in the study. Immunohistochemical expressions for p16 and p53 were evaluated and compared in all cases. The cases in the study were defined according to the Bethesda system. Of these, 31.8% (n = 27) had a low-grade squamous intraepithelial lesion (LGSIL), and 38.8% (n = 33) had a high-grade squamous intraepithelial lesion (HGSIL). RESULTS: There was a statistically significant difference between chronic cervicitis and CIN in terms of p53 and p16 expression levels (p = 0.001). On the other hand, the level of p16 expression was statistically different between LGSIL and HGSIL (p = 0.001), while there was no significant difference in terms of p53 expression. Among the HGSIL cases (n = 33), 91% had p16 expression, while 66.7% (n = 27) of the LGSIL patients had no p16 expression. In the chronic cervicitis group, 84% (n = 21) did not reveal any p16 expression, while 96% (n = 24) did not reveal any p53 expression. Various levels of p53 expressions were detected in 59.2% (n = 16) of CIN1 cases, 69.3% (n = 9) of CIN2 cases, and 90% (n = 18) of CIN3 cases. CONCLUSION: While p16 is useful in detecting high-grade cervical lesions, p53 is not a good biomarker for distinguishing high-grade lesions from low grade ones.


Asunto(s)
Biomarcadores de Tumor/análisis , Inhibidor p16 de la Quinasa Dependiente de Ciclina/metabolismo , Infecciones por Papillomavirus/metabolismo , Proteína p53 Supresora de Tumor/metabolismo , Displasia del Cuello del Útero/metabolismo , Neoplasias del Cuello Uterino/metabolismo , Adulto , Femenino , Perfilación de la Expresión Génica , Humanos , Inmunohistoquímica/métodos , Infecciones por Papillomavirus/virología , Medición de Riesgo , Sensibilidad y Especificidad , Índice de Severidad de la Enfermedad , Turquía , Neoplasias del Cuello Uterino/virología , Adulto Joven , Displasia del Cuello del Útero/virología
14.
Eur J Gynaecol Oncol ; 31(6): 719-21, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-21319528

RESUMEN

Adenomyosis is defined by the presence of endometrial tissue (glands and stroma) within the myometrium and malignant transformation of adenomyosis in premenopausal women with normal endometrium is extremely rare. Adenocarcinomas arising within adenomyosis need to be distinguished from endometrial carcinomas which arise from the eutopic endometrium, then extend into preexisting adenomyosis of the uterine wall. We report a case of grade 2 endometrioid adenocarcinoma arising from an adenomyotic focus in the uterus.


Asunto(s)
Carcinoma Endometrioide/patología , Neoplasias Endometriales/patología , Endometriosis/patología , Carcinoma Endometrioide/etiología , Neoplasias Endometriales/etiología , Endometriosis/complicaciones , Femenino , Humanos , Persona de Mediana Edad , Estadificación de Neoplasias , Pronóstico
15.
Clin Exp Obstet Gynecol ; 37(4): 269-72, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-21355455

RESUMEN

PURPOSE OF INVESTIGATION: To find the relationship between fetal Doppler findings and perinatal outcomes in intrauterine growth restriction. METHODS: Eighty-two cases with a prenatal diagnosis of intrauterine growth restriction between November 2008 and July 2009 were included in this prospective study at Ege University School of Medicine. Fetuses were grouped according to Doppler parameters: those with normal Doppler findings (n = 43), and those with impaired arterial (n = 27) and venous systems (n = 12). RESULTS: Out of 82 growth restricted cases, 43 (52.4%) had normal Doppler findings, while 27 (32.9%) displayed impaired arterial parameters and 12 (14.6%) had impaired venous parameters. The mean first minute Apgar scores were 7.57 +/- 1.53 for the group with normal Doppler flows, 6.8 +/- 2 for the group with an impaired arterial system, and 4 +/- 1.94 for the group with an impaired venous system. Two cases from the normal Doppler flow group (n = 42), four cases from the impaired arterial flow group (n = 27), and 11 cases from the impaired venous flow group (n = 11) had fifth minute Apgar scores under 6. Evaluation of the umbilical artery blood gas revealed acidosis in two cases from the normal Doppler flow group (n = 42), three cases from the impaired arterial system group (n = 27), and five cases from the impaired venous system group (n = 11). CONCLUSION: A Doppler spectrum from normal to venous system impairment correlated with poor fetal outcomes including fetal acidosis, fetal mortality and morbidity, decreased Apgar scores at 1 and 5 min, and neonatal morbidity.


Asunto(s)
Arterias/embriología , Retardo del Crecimiento Fetal/diagnóstico por imagen , Resultado del Embarazo/epidemiología , Ultrasonografía Prenatal , Venas/embriología , Puntaje de Apgar , Arterias/diagnóstico por imagen , Peso al Nacer , Velocidad del Flujo Sanguíneo , Análisis de los Gases de la Sangre , Femenino , Retardo del Crecimiento Fetal/fisiopatología , Edad Gestacional , Humanos , Recién Nacido , Embarazo , Estudios Prospectivos , Venas/diagnóstico por imagen
16.
Clin Exp Obstet Gynecol ; 37(4): 322-3, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-21355468

RESUMEN

PURPOSE OF INVESTIGATION: To evaluate placental growth factor as a screening test for gestational diabetes mellitus in the first trimester. METHODS: Sixty-seven pregnant women who were admitted to the outpatient clinic of Ege University Obstetrics and Gynecology Department consecutively for first trimester bioanalysis between May 2005 and February 2006 were included in the study. The cohort of patients underwent 50 g or 100 g oral glucose tolerance tests at the 24th week of pregnancy. Placental growth factor levels were analyzed by ELISA (human PGIF, ELIZA kit, Quantikine, R&D systems, USA) from the maternal blood collected at the time of first trimester screening. RESULTS: The study group of 15 patients with gestational diabetes were compared with a control group of 52 pregnant women with normal oral glucose tolerance tests. The level of placental growth factor was mean 35.79 +/- 16.79 pg/ml in the study group whereas it was mean 45,12 +/- 28.07 pg/ml in the control group. There was no significant difference between either group for placental growth factor maternal serum levels. CONCLUSION: Maternal placental growth factor serum levels are not useful in predicting gestational diabetes mellitus.


Asunto(s)
Diabetes Gestacional/sangre , Edad Gestacional , Tamizaje Masivo/métodos , Proteínas Gestacionales/sangre , Adulto , Peso al Nacer , Femenino , Prueba de Tolerancia a la Glucosa , Humanos , Factor de Crecimiento Placentario , Embarazo , Primer Trimestre del Embarazo
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