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6.
Br J Oral Maxillofac Surg ; 44(4): 317-9, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16213070

RESUMO

We operated on a 23-year-old black Nigerian man with a 4-year history of a tumour on the left cheek associated with IgE hypergammaglobulinaemia and peripheral eosinophilia. The lesion recurred.


Assuntos
Hiperplasia Angiolinfoide com Eosinofilia/cirurgia , Imunoglobulina E/sangue , Adulto , Hiperplasia Angiolinfoide com Eosinofilia/complicações , Hiperplasia Angiolinfoide com Eosinofilia/patologia , Bochecha , Humanos , Hipergamaglobulinemia/complicações , Masculino , Recidiva Local de Neoplasia
13.
J Cutan Pathol ; 24(7): 440-4, 1997 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-9274963

RESUMO

We present a new case of retiform hemangioendothelioma (RH), an entity first described by Calonje et al. in 1994. The tumor was intradermal and located on the toe of an 11-year-old boy. Histologically, in addition to the distinctive retiform pattern of proliferating vessels in RH there are intraluminal papillae with hyaline cores similar to those seen in malignant endovascular papillary angioendothelioma (Dabska's tumor), but usually they are infrequent, focal and poorly developed. In our case, these papillary structures were well formed and distributed in a diffuse way. They were most conspicuous in superficial areas where the blood vessels were dilated. In deep areas, where the pattern of neoplastic vessels was retiform, the papillae filled their lumina totally, resembling solid cords. Our case shares the clinical and morphologic features of both retiform hemangioendothelioma and Dabska's tumor, supporting a relationship between these two kinds of neoplasms. The benign behavior of this case, with no recurrence or metastases over a 4-year follow-up, corresponds to the low malignancy of this kind of vascular neoplasm.


Assuntos
Endotélio Vascular/patologia , Hemangioendotelioma/patologia , Neoplasias Cutâneas/patologia , Divisão Celular , Criança , Intervalo Livre de Doença , Hemangioendotelioma/irrigação sanguínea , Hemangioendotelioma/cirurgia , Humanos , Masculino , Neoplasias Cutâneas/irrigação sanguínea , Neoplasias Cutâneas/cirurgia , Dedos do Pé/patologia , Dedos do Pé/cirurgia
14.
J Cutan Pathol ; 25(1): 44-9, 1998 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-9508343

RESUMO

We report 5 cases of the fibrosarcomatous variant of dermatofibrosarcoma protuberans, 4 of which presented a morphologic change of intraneoplastic blood vessels not previously recognized. This change consisted of focal proliferation of smooth muscle cells, resulting in hypertrophy, generally eccentric, of vascular walls with reduction and collapsing of vascular lumina. In 3 cases the proliferation was so intense it formed leiomyomatous nodules and bundles. This proliferation may originate in the smooth muscle cells of the vessel walls either by means of a hyperplastic mechanism or in the pericytes via a line of differentiation leading to mature smooth muscle cells. In either case, we believe that it concerns a reactive process of the vessel walls very probably induced by adjacent neoplastic cells. The cases recently reported by Calonje and Fletcher as "myoid differentiation" of neoplastic cells in dermatofibrosarcoma protuberans (DFSP) may well be an expression of the same phenomenon, and therefore the presence of leiomyomatous areas in this tumor should not be used to support the theory of a fibroblastic/myofibroblastic line of differentiation for DFSP.


Assuntos
Dermatofibrossarcoma/patologia , Leiomioma/patologia , Músculo Liso Vascular/patologia , Neoplasias Cutâneas/patologia , Actinas/metabolismo , Adolescente , Adulto , Antígenos CD34/metabolismo , Dermatofibrossarcoma/irrigação sanguínea , Dermatofibrossarcoma/metabolismo , Desmina/metabolismo , Feminino , Humanos , Leiomioma/metabolismo , Masculino , Pessoa de Meia-Idade , Músculo Liso Vascular/metabolismo , Kit de Reagentes para Diagnóstico , Estudos Retrospectivos , Neoplasias Cutâneas/irrigação sanguínea , Neoplasias Cutâneas/metabolismo
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