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1.
Acta Neurochir (Wien) ; 149(12): 1229-36; discussion 1236-7, 2007 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17924056

RESUMO

Choroid plexus papillomas (CPP) are rare intracranial tumours with a favourable long-term outcome after surgical excision. Although they are histologically benign, local recurrences may occasionally occur, but leptomeningeal dissemination is exceptional. We report an unusual example of a fourth ventricle choroid plexus papilloma with diffuse leptomeningeal seeding. Neither the initial tumour nor the recurrence showed malignant histological features. Treatment with systemic and intrathecal chemotherapy was ineffective in this patient. We review the literature concerning leptomeningeal dissemination of benign choroid plexus papillomas.


Assuntos
Neoplasias do Ventrículo Cerebral/cirurgia , Quarto Ventrículo/cirurgia , Neoplasias Meníngeas/secundário , Inoculação de Neoplasia , Papiloma do Plexo Corióideo/cirurgia , Adulto , Biomarcadores Tumorais/análise , Biópsia , Neoplasias do Ventrículo Cerebral/patologia , Progressão da Doença , Evolução Fatal , Feminino , Quarto Ventrículo/patologia , Humanos , Antígeno Ki-67/análise , Laminectomia , Imageamento por Ressonância Magnética , Neoplasias Meníngeas/patologia , Neoplasias Meníngeas/cirurgia , Meninges/patologia , Papiloma do Plexo Corióideo/patologia , Reoperação , Proteínas S100/análise
2.
Neurocirugia (Astur) ; 18(2): 115-22, 2007 Apr.
Artigo em Espanhol | MEDLINE | ID: mdl-17497057

RESUMO

Chordoid glioma of the third ventricle is an infrequent brain tumour that was described for the first time by Brat et al. in 1998; since then, only 39 cases have been reported. We present a new case of chordoid glioma of the third ventricle in a 51-year-old-man that was treated with total surgical removal, with a good initial postoperative evolution. Sudden death, most likely due to a massive pulmonary embolism, occurred in the third postoperative day. We present the histological characteristics of the tumour and review the literature regarding this entity.


Assuntos
Neoplasias do Ventrículo Cerebral , Glioma , Terceiro Ventrículo/patologia , Neoplasias do Ventrículo Cerebral/diagnóstico , Neoplasias do Ventrículo Cerebral/patologia , Neoplasias do Ventrículo Cerebral/cirurgia , Evolução Fatal , Glioma/diagnóstico , Glioma/patologia , Glioma/cirurgia , Humanos , Masculino , Pessoa de Meia-Idade , Literatura de Revisão como Assunto , Terceiro Ventrículo/cirurgia
3.
Neurocir. - Soc. Luso-Esp. Neurocir ; 18(2): 115-122, mar.-abr. 2007. ilus, tab
Artigo em Es | IBECS | ID: ibc-70305

RESUMO

El glioma cordoide del tercer ventrículo es una entidadtumoral muy infrecuente descrita por primeravez en 1998 por Brat y colaboradores; desde entoncesse han descrito en la literatura tan sólo 39 casos. Presentamosun nuevo caso de glioma cordoide del tercerventrículo en un paciente varón de 51 años, que fuetratado mediante resección quirúrgica completa, conbuena evolución en el postoperatorio inmediato, peroque falleció súbitamente tres días después de la intervenciónpor un probable embolismo pulmonar. Presentamoslas características histológicas del tumor yrealizamos una revisión de la literatura


Chordoid glioma of the third ventricle is an infrequentbrain tumour that was described for the firsttime by Brat et al. in 1998; since then, only 39 caseshave been reported. We present a new case of chordoidglioma of the third ventricle in a 51-year-old-man thatwas treated with total surgical removal, with a good initialpostoperative evolution. Sudden death, most likelydue to a massive pulmonary embolism, occurred in thethird postoperative day. We present the histologicalcharacteristics of the tumour and review the literatureregarding this entity


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Neoplasias do Ventrículo Cerebral/diagnóstico , Glioma/diagnóstico , Terceiro Ventrículo/patologia , Neoplasias do Ventrículo Cerebral/cirurgia , Terceiro Ventrículo/cirurgia , Evolução Fatal , Glioma/cirurgia
6.
Arch Bronconeumol ; 36(9): 536-8, 2000 Oct.
Artigo em Espanhol | MEDLINE | ID: mdl-11116552

RESUMO

We report the case of a 24-year-old man with a diagnosis of bronchiolitis obliterans, a rare clinical condition; the similarity to Ardystil syndrome was striking. Relevant occupational history included work in a textile air-brushing factory. Also noteworthy were lesions observed by CT scan in the form of cystic formations measuring less than 1 cm, a finding not previously described in the context of bronchiolitis obliterans. The patient improved immediately after starting corticoid treatment although scans failed to improve over several months of follow-up.


Assuntos
Bronquiolite Obliterante/diagnóstico , Doenças Profissionais/diagnóstico , Adulto , Poluentes Ocupacionais do Ar/efeitos adversos , Bronquiolite Obliterante/diagnóstico por imagem , Bronquiolite Obliterante/patologia , Diagnóstico Diferencial , Humanos , Masculino , Doenças Profissionais/diagnóstico por imagem , Doenças Profissionais/patologia , Radiografia , Solventes/efeitos adversos , Indústria Têxtil
7.
Arch. bronconeumol. (Ed. impr.) ; 36(9): 536-538, oct. 2000.
Artigo em Es | IBECS | ID: ibc-4206

RESUMO

Presentamos el caso de un varón de 24 años de edad diagnosticado de bronquiolitis obliterante, entidad clinicopatológica infrecuente. Llama la atención la similitud con el síndrome de Ardystil. Entre los antecedentes profesionales se encuentra haber trabajado en una empresa de aerografía textil. También son destacables las lesiones radiológicas por tomografía axial computarizada, consistentes en formaciones quísticas de menos de 1 cm, no descritas con anterioridad en relación con la bronquiolitis obliterante. Diagnosticado el paciente, se inicia tratamiento con corticoides, con mejoría clínica inmediata, pero no radiológica, tras varios meses de seguimiento (AU)


Assuntos
Adulto , Masculino , Humanos , Solventes , Indústria Têxtil , Bronquiolite Obliterante , Diagnóstico Diferencial , Poluentes Ocupacionais do Ar , Doenças Profissionais
8.
Acta Otorrinolaringol Esp ; 49(1): 75-7, 1998.
Artigo em Espanhol | MEDLINE | ID: mdl-9557313

RESUMO

A case of laryngeal paraganglioma in a 65-year-old male was treated by supraglotic laryngectomy. This controversial tumor is analyzed and guidelines are given for its clinical and histological (immunohistochemical) diagnosis and treatment.


Assuntos
Neoplasias Laríngeas/diagnóstico por imagem , Neoplasias Laríngeas/patologia , Paraganglioma/diagnóstico por imagem , Paraganglioma/patologia , Idoso , Humanos , Neoplasias Laríngeas/cirurgia , Masculino , Paraganglioma/cirurgia , Radiografia
9.
Cir Pediatr ; 4(2): 96-102, 1991 Apr.
Artigo em Espanhol | MEDLINE | ID: mdl-2064900

RESUMO

We have carried out an experimental model of urinary diversion and dis-diversion on male Wistar rats in order to study the complications that are produced after diversion, as well as to see whether the alterations continue unchanged, or increase, or diminish after dis-diversion. The following experimental design was used: a control group made up of 48 animals an a problem group of 200 animals all submitted to vesicosigmoidostomy of which 100 were designed to be subsequently dis-diverted. The sacrificed animals (n = 112) were studied for somatic, biochemical and histological parameters. Statistical comparison of the problem group with the controls showed significant differences for the somatic and biochemical parameters, especially in the form of weight-size retardation, increase of urea, creatinine, calcium, phosphorus, uric acid, cholesterol, transaminase, alkaline phosphatase, sodium and chlorine and decrease in albumin and total proteins. After dis-diversion there is an improvement of some of these parameters without reaching total normalization. This leads us to think that either the lesions are irreversible, or more time after dis-diversion is needed for there to be reversibility. We also describe the histological lesions found at the level of the vesicointestinal anastomosis, and the mortality of our series which is higher than that presented by females, a fact inducing us to think that factors exist in the male which increase the mortality.


Assuntos
Complicações Pós-Operatórias/cirurgia , Doenças da Bexiga Urinária/cirurgia , Derivação Urinária/efeitos adversos , Animais , Colo Sigmoide/cirurgia , Modelos Animais de Doenças , Masculino , Complicações Pós-Operatórias/sangue , Complicações Pós-Operatórias/patologia , Ratos , Ratos Endogâmicos , Reoperação , Bexiga Urinária/cirurgia , Doenças da Bexiga Urinária/sangue , Doenças da Bexiga Urinária/patologia , Derivação Urinária/métodos
10.
Cir Pediatr ; 4(1): 3-7, 1991 Jan.
Artigo em Espanhol | MEDLINE | ID: mdl-2043432

RESUMO

Though there are not many cases described in the literature and very few for children, the existence of lower urodigestive communications may give rise to inflammatory processes in gonads and gonaducts in the male. We have carried out an experimental study of this aspect on 248 male Wistar rats according to the following design: A 48 animal control group (C) is divided into four equal subgroups sacrificed at the ages of one, two, three and four months. The problem group (P) of 200 animals are all submitted to vesicosigmoidostomy and then 100 are sacrificed after one and two months, and the other 100 are dis-diverted one and two months after the original diversion and sacrificed one month later. No histological alterations were observed in gonads and gonaducts for the sacrificed control animals (n = 48). The animals sacrificed after diversion (44 per 100) showed the following histological alterations: five cases of testicular tube necrosis, two cases of deferent conduit inflammation, one case of deferent conduit necrosis, 12 cases of epididymis inflammation and 13 cases of epididymis necrosis. The animals that also underwent dis-diversion and that were later sacrificed (20 per 100) showed: five cases of testicular tube necrosis, one case of testicular inflammation, two cases of deferent conduit inflammation, four cases of epididymis inflammation and seven cases of epididymis necrosis. Statistical analysis showed that the differences between the two P groups were not significant.(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Derivação Urinária/efeitos adversos , Animais , Colo Sigmoide/cirurgia , Masculino , Ratos , Ratos Endogâmicos , Contagem de Espermatozoides , Motilidade dos Espermatozoides , Testículo/patologia , Bexiga Urinária/cirurgia , Ducto Deferente/patologia
11.
Actas Urol Esp ; 14(2): 115-20, 1990.
Artigo em Espanhol | MEDLINE | ID: mdl-2378266

RESUMO

This paper is a review of 63 cases of congenital Pyeloureteral Union Syndrome. A total of 47 patients were treated using the Anderson-Hynes reconstructive technique with 3-4 years follow-up. Incidence was analyzed by sex, age and side affected, without a clear predominance of one over the others being shown. Mean age at the time of diagnosis was 39-43 years. The predominant symptom is the presence of lumbo-abdominal pain (36.5%) but the lack of clinical symptoms is also frequent (25.3%). Pyelocalyceal lithiasis is the most frequent secondary pathology (28.5%). U.I.V. appears to be an irreplaceable means for diagnosis, achieving with this technique 93.6% of diagnosis. Hydronephrosis, in different degrees, and absence of ureteral contrast are the urographic signs most commonly found: 66% and 61% respectively. Using the Anderson-Hynes technique a rete of 85% good results can be obtained, with few complications and achieving disappearance of clinical symptoms and morphofunctional normality in a high percentage. Anderson-Hynes dismembered ureteropyeloplasty seems to be the choice technique for conservative surgical treatment of the P.U.U. syndrome.


Assuntos
Hidronefrose/etiologia , Pelve Renal/anormalidades , Pelve Renal/cirurgia , Ureter/anormalidades , Ureter/cirurgia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Criança , Constrição Patológica/complicações , Constrição Patológica/diagnóstico por imagem , Constrição Patológica/cirurgia , Feminino , Fibrose , Seguimentos , Humanos , Hidronefrose/diagnóstico por imagem , Pelve Renal/patologia , Masculino , Pessoa de Meia-Idade , Radiografia , Estudos Retrospectivos , Síndrome , Ureter/patologia
12.
Arch Esp Urol ; 42(9): 928-30, 1989.
Artigo em Espanhol | MEDLINE | ID: mdl-2624498

RESUMO

Another two cases of bladder adenocarcinoma (ADC), seen in 1988, are described herein. The most important aspects relative to tumor origin--urothelial and embryonal--are discussed. We review its clinical features and diagnosis, not unlike those of transitional cell tumors, although histologically different. We underscore the therapeutic aspects and poor prognosis in most of the cases.


Assuntos
Adenocarcinoma/patologia , Neoplasias da Bexiga Urinária/patologia , Adenocarcinoma/embriologia , Idoso , Idoso de 80 Anos ou mais , Humanos , Masculino , Prognóstico , Neoplasias da Bexiga Urinária/embriologia
13.
Arch Esp Urol ; 42(2): 105-8, 1989 Mar.
Artigo em Espanhol | MEDLINE | ID: mdl-2735776

RESUMO

The present experimental study was carried out in 75 female Wistar rats. End-to-side vesicosigmoidostomy was performed in 65; the remaining 10 rats comprised the control group. Thirty-three rats were de-diverted at 1 and 2 months later. The site of the vesicosigmoid anastomosis was assessed histologically at 1, 2, and 3 months postoperatively in diverted rats, and at 1 and 2 months in de-diverted rats. Squamous metaplastic changes and variable degrees of transitional cell line neoplasm were observed in the diverted rats. Bladder changes did not regress significantly after de-diversion. No structural changes were observed at the level of the sigmoid. This experimental animal model confirms the oncogenic potential of mixing feces and urine, and shows that de-diversion does not achieve significant regression of bladder tumor lesions.


Assuntos
Neoplasias da Bexiga Urinária/etiologia , Derivação Urinária/efeitos adversos , Animais , Colo Sigmoide/cirurgia , Feminino , Ratos , Ratos Endogâmicos , Indução de Remissão , Neoplasias da Bexiga Urinária/patologia
17.
Mycopathologia ; 97(1): 9-16, 1987 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-3561472

RESUMO

Rhinosporidiosis is reviewed, and the first autochthonous case in Spain is presented (site: in the nasal cavity of a 19-year-old male from a rural background). Diagnosis was established morphologically after eliminating the possibilities of Cryptococcus neoformans, Coccidioides immitis, and Chrysosporium crescens. Clinico-pathological features are described. Preparations were stained with hematoxylin-eosin, PAS, and methenamine silver, and studied for fluorescence. Certain aspects of the epidemiology and diagnosis are commented upon.


Assuntos
Cavidade Nasal/patologia , Doenças Nasais/patologia , Rinosporidiose/patologia , Adulto , Humanos , Masculino , Rinosporidiose/microbiologia , Rhinosporidium/isolamento & purificação , Espanha
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