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1.
Diagn Cytopathol ; 44(7): 582-90, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27089849

RESUMO

Liquid-based cytology (LBC) has recently become the preferred method for urine cytology analysis, but differences with conventional cytology (CC) have been observed. The purpose of this study is to analyze these differences and the clinical relevance of non-atypical urothelial cell groups (UCG) in voided urine specimens. Reporting terminology is discussed. Initially, diagnostic categories from 619 LBC and 474 CC samples, reviewed by five different pathologists, were compared (phase 1). Five years after LBC was implemented and applying strict cytologic criteria for UCG diagnosis, 760 samples were analyzed (phase 2) and compared to previous LBC specimens. Diagnostic differences, interobserver variability and clinicopathological correlation with a 6-month follow-up, were analyzed. UCG increased from 6.5% with CC to 20.7% (218%, 3.2 fold, P < 0.0001) with LBC. This difference was not related to interobserver variability. Five years later, the rate of UCG had decreased to 13 2%. While 6% of cases with a negative cytology had urothelial carcinoma (UC) within 6 months of diagnosis, this percentage increased to 15.7% with UCG. The sensitivity of the UCG category for UC was low (30.4%), but the specificity and the negative predictive value (NPV) were high (87.1% and 94%, respectively). LBC increases UCG when compared to CC. This can be corrected with observers experience and using set cytological criteria. Due to its association with carcinoma, the presence of UCG in voided urine should be framed in a diagnostic category other than "negative for malignancy." Diagn. Cytopathol. 2016;44:582-590. © 2016 Wiley Periodicals, Inc.


Assuntos
Carcinoma/patologia , Urina/citologia , Neoplasias Urogenitais/patologia , Urotélio/patologia , Biópsia , Carcinoma/urina , Humanos , Sensibilidade e Especificidade , Neoplasias Urogenitais/urina
2.
Am J Dermatopathol ; 30(5): 431-5, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-18806483

RESUMO

Superficial acral fibromyxoma (SAF) is an uncommon tumor of the superficial soft tissues of acral extremities in middle-aged adults, firstly described in a series of 37 cases by Fetsch et al. in 2001. Since then, just a few case reports have been published. It is histologically characterized by a slightly to moderately cellular proliferation of spindled and stellate-shaped bland fibroblastic cells, arranged in a random, loose storiform, or fascicular growth pattern, within a myxoid, myxocollagenous, or collagenous stroma, with a prominent vasculature. The cells express CD34, CD99, and, frequently, epithelial membrane antigen. We report 4 cases that show clinical, morphological, and immunohistochemical characteristics of SAF and, additionally, exhibit two features rarely documented in previous publications, such as CD10 expression and a lipomatous component. Three of our 4 cases express CD10. The single previously reported case tested for CD10 was also positive. One of our cases contains mature fat cells intermingled with the spindle cells throughout the lesion. This finding has not been documented before in SAF. Our small series shows that SAF frequently expresses CD10 and occasionally can have a lipomatous component.


Assuntos
Adipócitos/patologia , Fibroma/metabolismo , Fibroma/patologia , Neprilisina/metabolismo , Neoplasias de Tecidos Moles/metabolismo , Neoplasias de Tecidos Moles/patologia , Antígeno 12E7 , Adulto , Antígenos CD/metabolismo , Antígenos CD34/metabolismo , Moléculas de Adesão Celular/metabolismo , Feminino , Fibroma/diagnóstico , Dedos , Regulação Neoplásica da Expressão Gênica , Humanos , Masculino , Pessoa de Meia-Idade , Mucina-1/metabolismo , Neprilisina/genética , Neoplasias de Tecidos Moles/diagnóstico , Dedos do Pé
3.
J Crohns Colitis ; 2(2): 114-22, 2008 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21172201

RESUMO

OBJECTIVES: Perinuclear anti-neutrophil cytoplasmic antibody (p-ANCA) and anti-Saccharomyces cerevisiae antibody (ASCA) have been proposed as markers for diagnosis and for subtyping of inflammatory bowel disease (IBD). The aim of this study was to investigate the association of p-ANCA and ASCA with a 10-year disease outcome in terms of cumulative rate of colectomy and relapse in a population-based European inception cohort of ulcerative colitis (UC) patients. METHODS: Serum samples from 432 consenting patients were analysed for p-ANCA and ASCA. The results were compared with the cumulative colectomy rate, relapsing disease and total number of relapses. We used multiple regression analyses adjusted for age, sex, residence, disease extent at diagnosis, smoking, familial IBD and drug treatment to study the relationship between serological values and disease course. RESULTS: The relapse rate was higher in the p-ANCA-positive patients: 82% (95% confidence interval [CI] 75-89%) compared with 67% (CI 62-72%, p=0.011) in the p-ANCA-negative patients. The risk of relapsing disease course was higher by a factor of 1.4 (CI 1.1-1.8, p=0.009) for p-ANCA-positive patients than for p-ANCA-negative patients, and the corresponding relative risk (RR) for the total number of relapses was 1.9 (CI 1.7-2.1, p<0.001). In ASCA-positive patients RR for the total number of relapses was 1.8 (CI 1.5-2.1, p<0.001). No significant association with colectomy rate was found for the presence of either p-ANCA or ASCA. CONCLUSION: UC patients positive for p-ANCA and possibly for ASCA may have a more unfavourable long-term disease outcome in terms of relapse than UC patients without these markers.

4.
Arch Neurol ; 62(4): 666-70, 2005 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15824270

RESUMO

BACKGROUND: l-2-Hydroxyglutaric aciduria is a rare, infantile-onset, autosomal recessive organic aciduria affecting exclusively the central nervous system. To our knowledge, only 1 complete report of the neuropathological findings in an adult has been published. OBJECTIVE: To present the clinical, neuroimaging, and neuropathological findings of l-2-hydroxyglutaric aciduria. DESIGN: Case report. SETTING: Complexo Hospitalario de Pontevedra, Pontevedra, Spain. PATIENT: A 15-year-old boy who had early infantile-onset progressive psychomotor regression, mild choreodystonia affecting the distal part of the upper limbs, pyramidal signs, and epilepsy. RESULTS: The diagnosis of l-2-hydroxyglutaric aciduria was confirmed by the finding of highly elevated levels of l-2-hydroxyglutaric acid in the serum, urine, and cerebrospinal fluid. The neuroimaging findings showed striking confluent subcortical white matter lesions and minimal basal ganglia (pallidum, thalamic, and putaminal) abnormalities. The patient died of a spontaneous mesenteric thrombosis. The postmortem neuropathological findings showed spongiosis and cystic cavitations in subcortical white matter, with minimal abnormalities of the basal ganglia. The dentate nucleus, a structure usually affected in neuroimaging studies, showed minimal neuronal loss but was surrounded by important spongiosis and microvacuolation with astrocytic proliferation. CONCLUSIONS: This case reaffirms that l-2-hydroxyglutaric aciduria is a spongiform type of leukoencephalopathy with cystic cavitations predominating in the subcortical areas. Although the neuroimaging findings are highly characteristic of the disease, in this patient cerebellar abnormalities were minimal and dentate signal abnormalities were not present.


Assuntos
Encefalopatias Metabólicas Congênitas/sangue , Encefalopatias Metabólicas Congênitas/patologia , Encéfalo/patologia , Encéfalo/fisiopatologia , Glutaratos/sangue , Glutaratos/urina , Adolescente , Atrofia/etiologia , Atrofia/patologia , Atrofia/fisiopatologia , Encéfalo/metabolismo , Encefalopatias Metabólicas Congênitas/urina , Epilepsia/etiologia , Epilepsia/metabolismo , Epilepsia/fisiopatologia , Evolução Fatal , Ácido Fólico/uso terapêutico , Genes Recessivos/genética , Glutaratos/líquido cefalorraquidiano , Humanos , Deficiência Intelectual/genética , Deficiência Intelectual/metabolismo , Deficiência Intelectual/patologia , Imageamento por Ressonância Magnética , Masculino , Oclusão Vascular Mesentérica/etiologia , Oclusão Vascular Mesentérica/patologia , Oclusão Vascular Mesentérica/fisiopatologia , Veias Mesentéricas/patologia , Veias Mesentéricas/fisiopatologia , Fibras Nervosas Mielinizadas/metabolismo , Fibras Nervosas Mielinizadas/patologia , Espanha
5.
Actas dermo-sifiliogr. (Ed. impr.) ; 95(6): 378-381, jul. 2004. ilus
Artigo em Es | IBECS | ID: ibc-33407

RESUMO

Las placas colágenas degenerativas de las manos son un trastorno adquirido, raro, habitualmente incluido entre las acroqueratodermias papulosas marginales. Se presenta un caso de placas colágenas degenerativas de las manos en una mujer de 44 años, con claros factores desencadenantes de tipo mecánico. Se exponen los hallazgos clínicos, histológicos y ultraestructurales, y se discute sobre la base de estos hallazgos su posición nosológica actual (AU)


Assuntos
Adulto , Feminino , Humanos , Dermatoses da Mão/patologia , Deformidades Adquiridas da Mão/patologia , Microscopia Eletrônica
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