Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
1.
Rev. bras. oftalmol ; 77(3): 153-155, May-June 2018. graf
Article in Portuguese | LILACS | ID: biblio-959085

ABSTRACT

Resumo A Síndrome de Good é uma síndrome paraneoplásica caracterizada pela associação de timoma e hipogamaglobulinemia, cursando com imunossupressão. Relatamos um caso raro de retinite por citomegalovírus em paciente com esta síndrome.


Abstract Good syndrome is a paraneoplastic syndrome characterized by the association of thymoma and hypogammaglobulinemia, with immunosuppression. We report a rare case of cytomegalovirus retinitis in a patient with this syndrome.


Subject(s)
Humans , Female , Middle Aged , Thymoma/complications , Cytomegalovirus Retinitis/etiology , Agammaglobulinemia/complications , Retina/diagnostic imaging , Retinal Diseases/diagnostic imaging , Thymoma/immunology , Immunoglobulin G/blood , Visual Acuity , Ganciclovir/administration & dosage , Ganciclovir/therapeutic use , Cytomegalovirus Retinitis/diagnosis , Cytomegalovirus Retinitis/drug therapy , Cytomegalovirus/immunology , Agammaglobulinemia/immunology , Diagnostic Techniques, Ophthalmological , Administration, Intravenous
2.
Medicina (B.Aires) ; 68(1): 43-47, ene.-feb. 2008. ilus, tab
Article in Spanish | LILACS | ID: lil-633513

ABSTRACT

El mediastino anterior es un sitio frecuente de localización de tumores ricos en elementos linfoides. La identificación correcta de cada entidad es de importancia en el tratamiento de los pacientes. En ocasiones puede plantearse el diagnóstico diferencial entre timoma y linfoma linfoblástico con fenotipo de precursor T (LLB-T). La Citometría de Flujo (CF) es una técnica complementaria útil para estos tumores de la cual se obtiene información cualitativa y cuantitativa. Revisamos 38 tumores mediastinales que tenían estudio de CF. Además comparamos los resultados de CF de timomas y tejido tímico normal con 42 casos de LLB-T de otras localizaciones anatómicas. De los 38 tumores mediastinales 6 eran lesiones benignas, 9 linfomas difusos de células grandes con fenotipo B (LDCG-B), 10 linfomas de Hodgkin (LH), 11 timomas y 2 LLB-T. En 24 casos la CF aportó información positiva, definiendo el inmunofenotipo de las células linfoides neoplásicas, o los linfocitos característicos que acompañan a los timomas. La CF en los 10 casos de LH y en 4 lesiones benignas permitió descartar otros tipos de linfoma (LDCG-B, LLB-T, etc.). Las marcaciones para CD3, CD4 y CD8 fueron las más útiles para el diagnóstico diferencial entre timomas y LLB-T. En conclusión, la CF es una técnica complementaria de utilidad que aporta información en lesiones mediastinales de manera rápida, requiriendo cantidades pequeñas de material, tanto para el diagnóstico inicial como para el monitoreo de estas enfermedades.


The anterior mediastinum is a common site of tumors with abundant lymphoid elements. Flow cytometry is a useful complementary technique to analyze this type of tumors, which provides qualitative and quantitative information. A differential diagnosis can be sometimes made between thymoma and precursor T-lymphoblastic lymphoma (T-LBL). Correct identification is of utmost importance for patient treatment. A total of 38 mediastinal tumors were analyzed, and samples were separated for flow cytometry. Flow cytometry data from thymomas and normal thymic tissue were compared with 42 cases of T-LBL from other anatomical locations. Among 38 mediastinal tumors, we found 6 benign lesions, 9 diffuse large B-cell lymphomas (DLBCL), 10 Hodgkin lymphomas (HL), 11 thymomas and 2 T-LL. Flow cytometry provided positive information in 24 cases, and defined lymphoid neoplastic cells immunophenotype or the typical lymphocytes accompanying thymomas. Flow cytometry helped differentiate 10 cases of HL and 4 benign lesions from other lymphomas (DLBCL, T-LBL, etc.). CD3, CD4 and CD8 expressions were most useful for the differential diagnosis of thymomas and T-LL. To conclude, flow cytometry is a valid complementary technique, which promptly provides information on mediastinal lesions, requiring small quantities of tissue for both early diagnosis and follow up of these diseases.


Subject(s)
Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Female , Humans , Male , Middle Aged , Young Adult , Antigens, CD/analysis , Biomarkers, Tumor , Flow Cytometry , Mediastinal Neoplasms/pathology , Thymoma/pathology , Thymus Neoplasms/pathology , /analysis , /analysis , /analysis , Hyperplasia , Mediastinal Neoplasms/genetics , Mediastinal Neoplasms/immunology , Phenotype , Retrospective Studies , T-Lymphocytes/immunology , Thymoma/genetics , Thymoma/immunology , Thymus Neoplasms/genetics , Thymus Neoplasms/immunology
3.
Journal of Korean Medical Science ; : 47-51, 1994.
Article in English | WPRIM | ID: wpr-189271

ABSTRACT

The cell surface molecule identified by a monoclonal antibody(TE-1) to human thymic epithelial cell showed the specificity for thymic epithelial cells of both the cortex and medulla. TE-1 reacted with the epithelial cells of normal thymus and thymoma in fresh frozen tissues. The antigen recognized by TE-1 was mostly confined to the cell surface membrane and arranged in reticular network with long processes between thymocytes. On immunohistochemical analysis, TE-1 did not recognize normal epithelial cells of the uterine cervix, skin and stomach, and neoplastic cells of squamous cell carcinoma and gastric adenocarcinoma, all of which were stained with anti-cytokeratin monoclonal antibody. Among the tumor cell lines tested with flow cytometry, most of epithelial and all of hematopoietic cell origin were not labeled with TE-1. In summary, TE-1 appears to be a monoclonal antibody against a surface antigen of human thymic epithelial cell that is immunohistologically different from known epithelial cell surface antigens reported so far.


Subject(s)
Animals , Humans , Mice , Antibodies, Monoclonal/biosynthesis , Antibody Specificity , Antigens, Surface/immunology , Epithelium/immunology , Fluorescent Antibody Technique , Immunoenzyme Techniques , Immunoglobulin G/immunology , Immunoglobulin Isotypes/immunology , Mice, Inbred BALB C , Neoplasms/immunology , Thymoma/immunology , Thymus Gland/immunology , Thymus Neoplasms/immunology , Tumor Cells, Cultured
SELECTION OF CITATIONS
SEARCH DETAIL