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1.
Diagn Cytopathol ; 33(1): 20-5, 2005 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15945083

RESUMO

Our objective was to evaluate the usefulness of cytomorphologic assessment in the accuracy of diagnosis of Hodgkin's disease (HD), using imprint cytological preparations over a 18-yr period. Imprint materials from 34 HD cases were reviewed using cytomorphological and immunocytochemical studies. Twenty-six cases (76.5%) were diagnosed to be HD and 6 cases (17.6%) were suspected to be HD, but 2 cases (5.9%) were cytologically diagnosed as reactive lesions, because of an insufficient number of Reed-Sternberg (RS) cells. The 6 suspected cases were definitively diagnosed as HD, using immunocytochemistry. Immunophenotyping of RS cells in 32 cases (excluding the two cases of reactive lesions) showed CD30+ in 31 (96.9%) cases, CD15+ in 22 (68.8%) cases and CD20+ in 12 (37.5%) cases. RS cells were immunophenotypically classified into five groups: A, (CD 30+, 15+, 20-) 15 (46.9%); B, (CD30+, 15-, 20-) 5 (15.6%); C, (CD 30+, 15+, 20+) 6 (18.8%); D, (CD30+, 15-, 20+) 5 (15.6%); and E, (CD30-, 15+, 20+) 1 (3.1%). Cytomorphologic differences in RS cells were identified between group D and other groups (CD15+ and/ or CD20-). The former had a low polymorphic shape (like popcorn), and the latter had a more classical polymorphic shape. Epstein-Barr virus (EBV)-latent membrane protein-1(LMP-1) was identified in 16 (50%) cases. LMP-1 expression was found not only in classic RS cells, but also in smaller variants. These variants did not match the morphologic criteria of RS cells, but expressed the common phenotype (CD30+, CD15+/-) of RS cells, suggesting the same cellular origin as RS cells. This study demonstrated that imprint cytology from lymph node biopsies can be a useful tool for the diagnosis and the evaluation of the cellular biology of HD.


Assuntos
Citodiagnóstico/métodos , Doença de Hodgkin/diagnóstico , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Antígenos CD20/análise , Criança , Feminino , Doença de Hodgkin/metabolismo , Humanos , Imuno-Histoquímica , Japão , Antígeno Ki-1/análise , Antígenos CD15/análise , Masculino , Pessoa de Meia-Idade , Células de Reed-Sternberg/química , Células de Reed-Sternberg/patologia , Reprodutibilidade dos Testes , Sensibilidade e Especificidade , Proteínas da Matriz Viral/análise
2.
Acta Cytol ; 46(5): 864-8, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12365220

RESUMO

BACKGROUND: Hyaluronan (HA) synthesis is frequently observed in malignant mesothelioma cells, whereas it is rarely found in lymphoma cells. Previous studies have reported that a high HA concentration in the serum was related to poor prognosis in lymphomas, although the mechanism was not elucidated. We recently encountered a case of anaplastic large cell lymphoma with an HA-rich, massive, lymphomatous effusion. Several studies were performed to clarify the character of this unusual lymphoma and to observe whether the lymphoma cells synthesized HA. CASE: A 59-year-old female was admitted with abdominal pain. Radiologic studies revealed a pleural effusion and paraaortic lymph node swelling. A biopsied specimen was compatible with anaplastic large cell lymphoma. Detailed cytologic observations revealed that the lymphoma cells in the pleural effusion had alcian blue-positive, productive material in the prominent Golgi area and microvillous structures on the surface. Further studies found that most of the lymphoma cells had HA-binding protein and expressed CD44 antigen, a receptor for HA. In addition, the HA concentration in the supernatant of the primary culture cells was extremely high and increased time dependently. CONCLUSION: These observations suggest that the lymphoma cells synthesized and released HA. Interactions of the released HA and CD44 on the surface might play an important role in the peculiar serosal growth of lymphoma cells.


Assuntos
Ácido Hialurônico/biossíntese , Linfoma Difuso de Grandes Células B/metabolismo , Linfoma Difuso de Grandes Células B/patologia , Derrame Pleural Maligno/patologia , Anaplasia/patologia , Antígenos de Neoplasias/análise , Antígenos de Neoplasias/imunologia , Biópsia , Núcleo Celular/ultraestrutura , Meios de Cultura/análise , Citoplasma/patologia , Evolução Fatal , Feminino , Complexo de Golgi/metabolismo , Soronegatividade para HIV , Humanos , Receptores de Hialuronatos/análise , Receptores de Hialuronatos/imunologia , Linfoma Difuso de Grandes Células B/química , Microvilosidades/metabolismo , Pessoa de Meia-Idade , Células Tumorais Cultivadas
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