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1.
Article de Anglais | MEDLINE | ID: mdl-31605593

RÉSUMÉ

BACKGROUND/AIM: C3 glomerulopathy (C3GP) defines a rare group of glomerulonephritis (GN), which could lead to end stage renal disease (ESRD). Histopathologic features of the disease have yet to be defined and the prognostic factors and optimal treatment are not fully known. The purpose of this study was to determine the demographic, histological change, treatment modalities and outcomes among patients with C3GP. MATERIAL AND METHOD: This retrospective observational study was conducted in the Department of Nephrology, Gazi University, Ankara, from 2013 to 2017. All patients with kidney biopsies fulfilling the criteria for C3GP were included in the study. RESULTS: Twenty-four patients with C3GP (50% male and of middle age - 43 years old) were enrolled in this study. 21% (5/24) patients developed ESRD. Renal biopsy findings such as crescent formation, glomerulo-sclerosis and tubular atrophy were similar in patients with ESRD, when compared to patients who did not develop ESRD. The treatment modalities of the patients were examined in two groups as MMF based and non-MMF based. The difference in the preservation of eGFR did not reach statistical significance between these two groups. The success rate of complete remission was similar between both groups. Serum creatinine levels >2.3 mg/dl at admission and need for renal replacement treatment (RRT) were associated with decreased renal survival. CONCLUSION: MMF based or non-MMF based treatments have similar efficacy in C3GP. Serum creatinine level higher than 2.3 mg/dl at the time of diagnosis and need for RRT during admission are a strong predictor of ESRD with high sensitivity and specificity.


Sujet(s)
Complément C3/immunologie , Glomérulonéphrite/immunologie , Glomérulonéphrite/thérapie , Adolescent , Adulte , Anticorps monoclonaux humanisés/administration et posologie , Anticorps monoclonaux humanisés/usage thérapeutique , Inhibiteurs du complément/administration et posologie , Inhibiteurs du complément/usage thérapeutique , Créatinine/sang , Antienzymes/administration et posologie , Antienzymes/usage thérapeutique , Femelle , Débit de filtration glomérulaire/physiologie , Glomérulonéphrite/complications , Glomérulonéphrite/anatomopathologie , Humains , Défaillance rénale chronique/étiologie , Mâle , Adulte d'âge moyen , Acide mycophénolique/administration et posologie , Acide mycophénolique/usage thérapeutique , Induction de rémission , Traitement substitutif de l'insuffisance rénale/méthodes , Études rétrospectives , Résultat thérapeutique , Jeune adulte
2.
Hum Exp Toxicol ; 38(12): 1366-1377, 2019 Dec.
Article de Anglais | MEDLINE | ID: mdl-31280613

RÉSUMÉ

OBJECTIVES: Colistin is a vital antibiotic used in multidrug-resistant infections. Its most important side effect is nephrotoxicity. Colistin is a weak acid. This study aims to evaluate whether urine alkalinization is protective in the nephrotoxicity of colistin. METHODS: Twenty-eight male Sprague-Dawley rats were divided into groups. Group I (n = 4) was injected with intramuscular distilled water twice a day for 7 days. Group II (n = 8) was injected with 750,000 IU/kg/day colistin for 7 days. Group III (n = 8) was injected with the same dose of colistin after their urinary pH was ≥7 through the addition of bicarbonate in their drinking water. Group IV (n = 8) was injected with the same dose of colistin after their urine density fell below 1010 through the addition of NaCl molds in their food and 12.6 mg/L NaCl in their drinking water. RESULTS: According to tubular degenerations (scored 0-5), group I scored 0, group II scored 4.25, group III scored 2, and group IV scored 1.5. In groups III and IV, protection was achieved (p = 0.001). The bicarbonate group was not superior to the NaCl group (p = 0.789). In transmission electron microscopy, group III had more microvilli integrity and autophagic vacuoles compared to group IV. Group IV had mitochondrial swelling and cristae lysis. A lower urine density was related to lower tubular scores (p = 0.001). CONCLUSIONS: Colistin was highly nephrotoxic without protection. Light microscopy findings revealed that urinary alkalinization and NaCl hydration were similarly protective. Urine alkalinization further prevents ultrastructural changes as revealed by electron microscopy.


Sujet(s)
Antibactériens/toxicité , Hydrogénocarbonates/pharmacologie , Colistine/toxicité , Maladies du rein/prévention et contrôle , Chlorure de sodium/pharmacologie , Urine/composition chimique , Animaux , Concentration en ions d'hydrogène , Rein/effets des médicaments et des substances chimiques , Rein/anatomopathologie , Rein/ultrastructure , Maladies du rein/induit chimiquement , Maladies du rein/anatomopathologie , Mâle , Microscopie électronique à transmission , Rat Sprague-Dawley
3.
APMIS ; 127(9): 607-615, 2019 Sep.
Article de Anglais | MEDLINE | ID: mdl-31243811

RÉSUMÉ

Poorly differentiated chordoma (PDC) is a newly described variant of chordomas, which is not considered as a subtype yet, but has its own distinct features in terms of morphology, immunohistochemical and molecular characteristics, and clinical outcome. To provide a brief review of clinical, morphological, immunohistochemical, and molecular features of poorly differentiated chordoma. PubMed search using keyword 'poorly differentiated chordoma'. A critical review of all studies with a total of 53 cases using inclusion criteria of involvement of axial skeleton (vertebra and clivus), INI1 loss (either with the aid of immunohistochemistry or various molecular techniques), and immunohistochemical brachyury expression. PDC is characterized by a young population with slight female predominance, clivus/cervix location, multinodular sheets of epithelioid cells with eosinophilic cytoplasm and prominent pleomorphism, and loss of SMARCB1/INI1 expression, which can be demonstrated both with immunohistochemical and molecular studies, and is unexpected for other types of chordoma. However, classical chordomas lacking SMARCB1/INI1 expression were also reported and how to classify these cases has not been addressed yet. This unique entity is a candidate to be recognized and distinguished from other types of chordoma or SMARCB1-deficient tumors which are clinically important differential diagnoses that represent a challenging task for the pathologists.


Sujet(s)
Chordome/diagnostic , Chordome/anatomopathologie , Diagnostic différentiel , Cellules épithélioïdes/anatomopathologie , Femelle , Humains , Immunohistochimie/méthodes
4.
Indian J Cancer ; 54(1): 321-325, 2017.
Article de Anglais | MEDLINE | ID: mdl-29199714

RÉSUMÉ

BACKGROUND: Synovial sarcoma (SS) is a malignant mesenchymal tumor, which comprises 5%-10% of all the sarcomas. There is insufficient information on prognostic factors and salvage treatments of advanced SS. In this study, we aimed to further clarify the clinicopathological features, prognostic factors, and treatment modalities in advanced SS. MATERIALS AND METHODS: A total of 45 SS patients followed up between 2001 and 2015 at our cancer institute, Department of Medical Oncology, were retrospectively evaluated. Eleven patients were initially metastatic, and remaining patients developed metastasis or became inoperable due to locally advanced disease. Overall survival was evaluated by Kaplan-Meier analysis. RESULTS: The median age of patients was 37 (17-70) years and 60% (n = 26) of them were female. SS was most commonly localized in the lower extremity and abdomen-pelvis (29% and 29%, respectively). Median follow-up time was 33 (6-175) months. Patients were treated with a median of two (1-5) line chemotherapies at metastatic stage. Ifosfamide plus adriamycin (IMA) (49%, n = 22) and cisplatin-etoposide (13%, n = 6) were the most often used chemotherapy regimen as first line in metastatic stage. Partial response was obtained in 32% of the patients treated with IMA chemotherapy. Furthermore, median progression-free survival was 6 (1-123) months. Median survival of metastatic stage at diagnosis or in follow-up was 21 months (14-27) and 21 (12-29) months (P = 0.53), respectively. Most metastatic locations were lung (75%) and bone. Factors influencing survival at metastatic stage were evaluated; statistically significant longer survival was observed in patients with lung metastasis, primary tumor size smaller than 10 cm, patients who underwent surgery for the metastasis, and development-to-metastasis period longer than 12 months. CONCLUSION: Median survival of patients in metastatic stage SS was 21 months. Lung was the most common metastatic site.


Sujet(s)
Pronostic , Sarcome synovial/traitement médicamenteux , Sarcome synovial/radiothérapie , Adolescent , Adulte , Sujet âgé , Protocoles de polychimiothérapie antinéoplasique/administration et posologie , Cisplatine/administration et posologie , Association thérapeutique , Survie sans rechute , Doxorubicine/administration et posologie , Étoposide/administration et posologie , Femelle , Études de suivi , Humains , Ifosfamide/administration et posologie , Mâle , Adulte d'âge moyen , Métastase tumorale , Sarcome synovial/anatomopathologie , Jeune adulte
5.
PLoS One ; 9(10): e111446, 2014.
Article de Anglais | MEDLINE | ID: mdl-25333736

RÉSUMÉ

BACKGROUND: The term "Defensive" medicine was coined in the early 1970's and has been an important topic of scientific investigation and professional debate ever since. OBJECTIVE: The aim of this study was to investigate the characteristics of defensive medicine, its reasons, and the extent to which it is practiced in the Turkish health care system. This is the first national survey to study the practice of defensive medicine among neurosurgeons in Turkey. METHODS: The present cross-sectional study on defensive medicine assessed neurosurgeons registered at the Turkish Neurosurgical Society, who are actively working in various centers and hospitals within the Turkish health care system. A 40-question survey was adapted from existing measures described in the literature and was completed by a total of 404 neurosurgeons, representing 36.7% of the neurosurgeons registered at the Turkish Neurosurgical Society. RESULTS: Seventy-two percent of the participants in the current study reported practicing defensive medicine. This practice was mainly reported among inexperienced neurosurgeons (74.4%). Most were younger than 40 years of age (75.2%), working in state hospitals/universities (72.7%), and living in the Marmara region (38%). Respondents reported engaging in defensive medicine by avoiding high-risk surgery (62.6%), ordering additional imaging studies (60.9%) and laboratory tests (33.7%), and referring patients to consultants (31.2%). Most participants consider every patient as a potential threat in terms of a medical lawsuit (68.3%) and do not believe the courts can distinguish malpractice from complications (89.6%). CONCLUSION: Concerns and perceptions about medical liability lead neurosurgeons to practice defensive medicine. By avoiding high-risk surgery, ordering unnecessary diagnostic tests, and referring the patients to consultants, neurosurgeons try to minimize the risk of malpractice and protect themselves from legal risks, resulting in higher healthcare expenditure and longer treatment periods.


Sujet(s)
Attitude du personnel soignant , Assurance responsabilité civile , Neurochirurgiens/éthique , Adulte , Femelle , Humains , Mâle , Faute professionnelle/économie , Faute professionnelle/législation et jurisprudence , Adulte d'âge moyen , Neurochirurgiens/économie , Neurochirurgiens/législation et jurisprudence , Neurochirurgie/économie , Neurochirurgie/éthique , Neurochirurgie/législation et jurisprudence , Turquie
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