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1.
J Small Anim Pract ; 59(11): 714-718, 2018 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-29355995

RESUMO

A 14-month-old female pitbull terrier mix was presented for evaluation of dysphagia of 8 months' duration secondary to intermittent dorsiflexion of the tongue apex. Physical and neurological examinations were unremarkable with the exception of the dorsiflexed tongue. Serum creatine kinase activity was increased (703 IU/L, reference interval: 55 to 257 IU/L), and electromyography of the tongue demonstrated areas of fibrillation potentials. Histopathology of the tongue showed myopathic changes with excessive variability in myofibre size and endomysial fibrosis. Cytochemical stains verified mixed mononuclear cells throughout the endomysium and perimysium consistent with a chronic inflammatory myopathy. No improvement was reported following prednisone administration; although the dog was able to prehend kibble, it needed assistance when drinking water. This is the first report documenting a focal lingual myopathy in a non-corgi breed and highlights the utility of determining creatine kinase activity and obtaining tongue biopsies when warranted in dysphagic animals.


Assuntos
Transtornos de Deglutição/veterinária , Doenças do Cão/fisiopatologia , Miosite/veterinária , Doenças da Língua/veterinária , Animais , Creatina Quinase/metabolismo , Transtornos de Deglutição/etiologia , Transtornos de Deglutição/patologia , Doenças do Cão/enzimologia , Doenças do Cão/patologia , Cães , Feminino , Miosite/complicações , Miosite/enzimologia , Miosite/patologia , Língua/patologia , Doenças da Língua/enzimologia , Doenças da Língua/etiologia , Doenças da Língua/patologia
2.
J Contemp Dent Pract ; 16(2): 107-11, 2015 02 01.
Artigo em Inglês | MEDLINE | ID: mdl-25906800

RESUMO

BACKGROUND: Matrix metalloproteinase-3 (MMP-3) plays a key role in development of cancer. The purpose of this study was to assess MMP-3 in the serum and saliva of patients with oral lichen planus (OLP) and oral squamous cell carcinoma (OSCC). MATERIALS AND METHODS: Thirty patients with OLP (8 reticular and 22 erosive forms), and 20 patients with OSCC (6 in low stage and 14 in advanced stage), were enrolled in this study, conducted at the Cancer Department, Clinic of Oral Medicine, Tehran University of Medical Sciences. The serum and saliva MMP-3 was assayed by ELISA method. Statistical analysis of the Student's t-test, ANOVA and Pearson correlation coefficient was performed. The mean saliva and serum levels of MMP-3 were significantly higher in patients with OSCC compared with OLP. RESULTS: The serum and saliva MMP-3 concentrations increased from reticular form of OLP to erosive form of OLP, and increased further to low stage of OSCC and advanced stage of OSCC. Serum MMP-3 correlated significantly with unstimulated (r = 0.310, p = 0.038) and stimulated (r = 0.365, p < 0.026) saliva MMP-3. CONCLUSION: Serum and saliva MMP-3 levels appear associated with OLP and OSCC.


Assuntos
Carcinoma de Células Escamosas/enzimologia , Líquen Plano Bucal/enzimologia , Metaloproteinase 3 da Matriz/sangue , Neoplasias Bucais/enzimologia , Saliva/enzimologia , Adulto , Idoso , Carcinoma de Células Escamosas/sangue , Feminino , Doenças da Gengiva/sangue , Doenças da Gengiva/enzimologia , Humanos , Líquen Plano Bucal/sangue , Neoplasias Labiais/sangue , Neoplasias Labiais/enzimologia , Masculino , Metaloproteinase 3 da Matriz/análise , Pessoa de Meia-Idade , Neoplasias Bucais/sangue , Estadiamento de Neoplasias , Doenças da Língua/sangue , Doenças da Língua/enzimologia , Neoplasias da Língua/sangue , Neoplasias da Língua/enzimologia
3.
Artigo em Inglês | MEDLINE | ID: mdl-16632275

RESUMO

Cowden syndrome is a rare condition defined by multiple hamartomatous growths and a guarded prognosis owing to the high risk of cancer development. The syndrome is inherited as an autosomal dominant trait with incomplete penetrance and variable expressivity. The PTEN/MMAC1/TEP1 tumor suppressor gene on chromosome 10q23.3, has proven to contain a germline mutation predisposing for uncontrolled cell growth and survival via the PI3K/AKT pathway. Presented here is a case of Cowden syndrome in a patient with multiple hamartomas of the nose, midfacial skin and oral mucosa, and fissured tongue; plus a history of bipolar disease, iron deficiency anemia, basal cell carcinoma, fibroids of the uterus, and arthritis. The family history was significant for a daughter diagnosed with lung cancer. A final diagnosis of Cowden syndrome was made on the basis of established criteria and confirmed using immunohistochemistry directed against PTEN and phosphorylated-AKT.


Assuntos
Síndrome do Hamartoma Múltiplo/patologia , Mucosa Bucal/patologia , Dermatopatias/patologia , Doenças da Língua/patologia , Anti-Inflamatórios não Esteroides/farmacologia , Feminino , Expressão Gênica/efeitos dos fármacos , Regulação Enzimológica da Expressão Gênica , Mutação em Linhagem Germinativa , Síndrome do Hamartoma Múltiplo/enzimologia , Síndrome do Hamartoma Múltiplo/genética , Humanos , Técnicas Imunoenzimáticas , Pessoa de Meia-Idade , Mucosa Bucal/química , Mucosa Bucal/enzimologia , PTEN Fosfo-Hidrolase/análise , PTEN Fosfo-Hidrolase/genética , Proteínas Proto-Oncogênicas c-akt/análise , Dermatopatias/enzimologia , Doenças da Língua/enzimologia
4.
Jikken Dobutsu ; 36(4): 395-8, 1987 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-3436372

RESUMO

Spontaneously occurring calcified lesions were found in the tongues of DBA/2NCrj and CBA/BrA mice. In the DBA/2NCrj strain, the frequency of the lesion was 80% (males) and 88% (females). The youngest age of a mouse with this lesion was 18 days after birth, and 3-4 lesions were found in the tongue of 6- to 8-week-old mice. In CBA/BrA mice, 20% of females and 48% of males had the lesions. No significant differences were found in the serum calcium concentrations in high and low lesion-developing strains, but the alkaline phosphatase activities in the high-developing DBA/2NCrj, DBA/LiA, and CBA/BrA strains were higher than in strains with no calcified lesions.


Assuntos
Fosfatase Alcalina/sangue , Calcinose/veterinária , Camundongos Endogâmicos CBA/sangue , Camundongos Endogâmicos DBA/sangue , Doenças dos Roedores/enzimologia , Doenças da Língua/veterinária , Animais , Calcinose/enzimologia , Cálcio/sangue , Feminino , Masculino , Camundongos , Fosfatos/sangue , Doenças da Língua/enzimologia
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