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1.
Clin Nephrol ; 100(3): 107-114, 2023 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-37485880

RESUMO

PURPOSE: Alterations in skin structure and function are very common in uremic patients, but still there is no unifying hypothesis for uremic skin disorders. Fibroblast growth factor-23 (FGF-23) deficiency has been linked to skin disorders in non-uremic animals. We aimed to study alterations in FGF-23 and fibroblast growth factor-23 receptor 1 (FGFR1) expression in uremic rat skins. MATERIAL AND METHODS: Wistar albino rats were divided into two groups: sham group (SG, n = 8) and uremic group (UG, n = 8). Uremia was induced by reduction of the total kidney mass in the UG. Animals were sacrificed after 14 weeks of the follow-up. RESULTS: Serum creatinine and blood urea nitrogen levels in the UG increased significantly, compared to the SG, at the end of the experiment (0.69 ± 0.08 vs. 0.3 ± 0.04 Mann-Whitney U test (MWU), p = 0,003 and 55.2 ± 8.9 vs. 29.6 ± 6.8 MWU, p = 0.002, respectively). Serum FGF-23 level in the UG was increased non-significantly, compared to the SG (53.5 ± 20.9 vs. 37.2 ± 9.7 MWU, p = 0.072), whereas serum 1,25(OH)2D3 level was significantly lower in the UG (149.4 ± 33.5 vs. 213.8 ± 43.8 MWU, p < 0.05). Expression of FGF-23 in UG skins, assessed by western blot, was significantly higher than that in the SG (186.3 ± 16.8 vs. 148.9 ± 25.9, MWU, p < 0.01). FGFR1 expression was increased in almost all parts of the uremic skin. Receptor expression was most dense at the epidermis and hair follicles. Normal skin appendages and cells either expressed no receptor, or expressed it very weakly. CONCLUSION: This study shows increased FGF-23 levels and FGFR1 expression in uremic rat skins. It deserves further study to fully place this finding in the pathophysiology and clinical picture of uremic skin diseases.


Assuntos
Insuficiência Renal , Uremia , Ratos , Humanos , Animais , Fator de Crescimento de Fibroblastos 23 , Ratos Wistar , Expressão Gênica , Receptor Tipo 1 de Fator de Crescimento de Fibroblastos
2.
J Clin Pediatr Dent ; 34(4): 351-4, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20831140

RESUMO

OBJECTIVE: Klippel-Trénaunay syndrome (KTS) is characterized by triad of venous varicosity, naevus flammeus, and soft/hard tissue hypertrophy. Manifestations of the syndrome in the head and neck region are rare, but in some cases hemangioma of the lips, tongue, and gums, open bite and cross bite, and early tooth eruption are associated with the disease. STUDY DESIGN: We report a 12-year-old KTS patient with gingival hyperplasia, congenital missing teeth, and increased mucosal vascularization as oral manifestations. RESULTS AND CONCLUSION: All manifestations of the KTS were observed on the same side of the head, except bilateral missing teeth. Histological examination showed several vascular enlargements in enlarged gingiva. It is suggested that oral manifestations of the syndrome are generally related to the severity of the disease, but they do not always present in the same pattern.


Assuntos
Anodontia/patologia , Crescimento Excessivo da Gengiva/patologia , Síndrome de Klippel-Trenaunay-Weber/patologia , Dente Pré-Molar/anormalidades , Capilares/patologia , Criança , Células Epiteliais/patologia , Gengiva/irrigação sanguínea , Humanos , Hipertrofia , Lábio/irrigação sanguínea , Lábio/patologia , Masculino , Plasmócitos/patologia
3.
Arch Pediatr ; 12(12): 1734-41, 2005 Dec.
Artigo em Francês | MEDLINE | ID: mdl-16219450

RESUMO

Autism is defined by 3 main criteria: disturbance of reciprocal social interaction, disturbance of communication (including language comprehension and spoken language) and disturbance of normal variation in behaviour and imaginative activities; an onset before age 36 months is also required. The neuropediatric contribution to autism is dominated by the search for an underlying organic etiology, especially if there are arguments for an associated encephalopathy: ante- or perinatal medical history, dysmorphic signs, skin spots, neurological abnormalities, somatic abnormalities compatible with a neurometabolic disorder. The main associated conditions with autism are: chromosome anomalies, monogenic syndrome (including fragile X syndrome), neurocutaneous syndromes, epileptic encephalopathies, neurometabolic diseases, and dystrophinopathies. The identification of an associated medical condition to autism is primordial in prospect of genetic counselling, and by the change induced in familial perception of autism.


Assuntos
Transtorno Autístico/diagnóstico , Transtorno Autístico/fisiopatologia , Pediatria , Transtorno Autístico/genética , Criança , Aberrações Cromossômicas , Diagnóstico Diferencial , Relações Familiares , Aconselhamento Genético , Humanos , Imageamento por Ressonância Magnética , Neurologia , Fatores de Risco
4.
BJU Int ; 93(7): 1087-93, 2004 May.
Artigo em Inglês | MEDLINE | ID: mdl-15142169

RESUMO

OBJECTIVE: To determine if use of cell proliferation, cell adhesion, level of angiogenesis-related factors and presence of microscopic vascular invasion (MVI) could better predict the biological behaviour of renal cell carcinoma (RCC), which has a widely variable clinical outcome despite the use of conventional prognostic factors (staging and grading). MATERIALS AND METHODS: The expression of Ki-67, CD44H and vascular endothelial growth factor (VEGF) were assessed immunohistochemically in formalin-fixed, paraffin-embedded tissues from 48 RCCs, using a Ki-67 labelling index (LI), CD44 LI and level of VEGF expression, respectively. In addition all the pathological slides were reviewed retrospectively for the presence and absence of MVI. The prognostic value of all the variables assessed was then evaluated, and correlated with the usual prognostic variables and cancer-specific survival. RESULTS: Univariate analysis of cancer-specific survival showed that tumour stage (P < 0.001), tumour size (P = 0.005), metastasis, MVI, Ki-67 LI, CD44H LI and VEGF expression (all P < 0.001) were predictors of tumour-related death. There was a statistical correlation between CD44H LI and each of Ki-67 LI (r = 0.61), expression level of VEGF (r = 0.72) and presence of MVI (r = 0.71). Independent predictors of cancer-specific survival in a multivariate analysis were: in all patients with RCC, the MVI (P = 0.003) and VEGF expression (P = 0.01); in those with no metastases, MVI (P = 0.01); in patients with no MVI, VEGF (P = 0.04); and in patients with MVI, Ki-67 LI (P = 0.003). No independent predictor was identified in patient with metastases. CONCLUSION: This study suggests that cell proliferation, cell adhesion, the level of VEGF expression and the presence of MVI represent a complex tumour-host interaction that may favour the progression of RCC. Cell proliferation, CD44H and VEGF expression appear to be powerful markers for identifying patients with an adverse prognosis.


Assuntos
Carcinoma de Células Renais/metabolismo , Receptores de Hialuronatos/metabolismo , Antígeno Ki-67/metabolismo , Neoplasias Renais/metabolismo , Proteínas de Neoplasias/metabolismo , Fatores de Crescimento do Endotélio Vascular/metabolismo , Adulto , Idoso , Idoso de 80 Anos ou mais , Carcinoma de Células Renais/irrigação sanguínea , Feminino , Humanos , Imuno-Histoquímica , Neoplasias Renais/irrigação sanguínea , Masculino , Microcirculação , Pessoa de Meia-Idade , Prognóstico , Análise de Sobrevida
5.
Mikrobiyol Bul ; 25(3): 247-55, 1991 Jul.
Artigo em Turco | MEDLINE | ID: mdl-1762592

RESUMO

The frequency of female genital tract tuberculosis exhibits a parallelism that of pulmonary tuberculosis in the population. It is generally found in reproductive women, but also occurs in postmenopausal ones. Its frequency has declined since the introduction of specific treatment, but it is discovered incidentally during the course of an investigation for infertility. The most common location is in fallopian tubes. In the Department of Pathology from the Medical School of Cumhuriyet University 11 female genital tract tuberculosis have been described between the years of 1984 and 1990. In this study, age, symptoms, localizations and pathological findings of these cases have been reviewed.


Assuntos
Tubas Uterinas/patologia , Tuberculose dos Genitais Femininos/epidemiologia , Adolescente , Adulto , Fatores Etários , Feminino , Humanos , Pessoa de Meia-Idade , Prevalência , Estudos Retrospectivos , Tuberculose dos Genitais Femininos/patologia , Turquia/epidemiologia
6.
Fundam Clin Pharmacol ; 3(1): 37-46, 1989.
Artigo em Inglês | MEDLINE | ID: mdl-2714731

RESUMO

[3H]52770 RP, a PAF antagonist, was found to bind with high affinity and in a reversible manner on specific and saturable binding sites in guinea pig cortical membranes. Scatchard analysis revealed the presence of one class of binding sites with an equilibrium dissociation constant of 0.38 nM and a Bmax of 1190 fmol/mg protein. However, these binding sites did not correspond to the PAF receptors described with this ligand in platelet plasma membranes; indeed, PAF and its analogs were unable to displace [3H]52770 RP binding in guinea pig brain. Therefore, one may conclude that [3H]52770 RP in guinea pig brain labels acceptor or recognition sites, rather than true receptor sites.


Assuntos
Antibacterianos , Antibióticos Antituberculose/metabolismo , Encéfalo/metabolismo , Fator de Ativação de Plaquetas/antagonistas & inibidores , Receptores de Droga/metabolismo , Animais , Antibióticos Antituberculose/farmacocinética , Cátions/farmacologia , Córtex Cerebral/metabolismo , Cobaias , Técnicas In Vitro , Masculino , Membranas/metabolismo , Peptídeos/metabolismo , Peptídeos/farmacocinética , Proteínas/metabolismo , Estereoisomerismo
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