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2.
J Cutan Pathol ; 35(3): 278-84, 2008 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-18251741

RESUMO

BACKGROUND: It has been shown that the 3G5 antigen recognized by monoclonal antibody 3G5 (mAb 3G5) is a useful marker of pericytes in normal human skin. However, most 3G5 antigen-expressing cells in capillary vessels were stained negatively for alpha-smooth muscle actin (alpha-SMA), a prominent pericyte marker. This study was designed to determine whether the expression of the 3G5 antigen is restricted to specific stages of pericyte development, or if it is expressed in other cells rather than pericytes in capillary vessels. METHODS: 3G5 antigen-expressing cells were detected in normal human skin, granulating tissues from decubitus ulcers and inflammatory psoriatic skin with extensive angiogenesis using double immunofluorescent staining with mAb 3G5 and monoclonal antibodies (mAbs) to various pericyte markers, tryptase and chymase. Furthermore, using immunoelectron microscopy, 3G5 antigen-expressing cells were observed in the granulating tissues. RESULTS: The immunoelectron microscopic findings and double immunofluorescent staining (using mAb 3G5 and either anti-tryptase or anti-chymase mAbs) showed that 3G5 antigen-expressing cells were mast cells in normal skin, granulating tissues and psoriatic skin. CONCLUSIONS: The results indicated that 3G5 antigen is a marker of mast cells, but not of pericytes in normal and diseased skin.


Assuntos
Anticorpos Monoclonais/imunologia , Gangliosídeos/metabolismo , Tecido de Granulação/metabolismo , Mastócitos/metabolismo , Pericitos/metabolismo , Pele/metabolismo , Biomarcadores/metabolismo , Quimases/imunologia , Técnica Indireta de Fluorescência para Anticorpo , Gangliosídeos/imunologia , Tecido de Granulação/patologia , Humanos , Mastócitos/ultraestrutura , Microscopia Imunoeletrônica , Pericitos/ultraestrutura , Úlcera por Pressão/metabolismo , Úlcera por Pressão/patologia , Psoríase/metabolismo , Psoríase/patologia , Pele/patologia , Triptases/imunologia
3.
J Dermatol ; 33(2): 115-7, 2006 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16556279

RESUMO

A 64-year-old male who cultivated orchids as a hobby, had noticed itchy erythematous lesions on both hands since 6 months earlier. His eruptions had gradually worsened and scales and fissures had appeared. Although he was treated with topical corticosteroids by a doctor, his erythema showed no improvement. Patch tests with the orchids he cultivated, fertilizers, antiseptics and insecticides showed positive reactions to the stems of Cymbidium and Oncidium orchids. A diagnosis of contact dermatitis attributable to the cultivated orchids was made.


Assuntos
Dermatite Alérgica de Contato/etiologia , Exposição Ocupacional/efeitos adversos , Orchidaceae/efeitos adversos , Dermatite Alérgica de Contato/diagnóstico , Seguimentos , Dermatoses da Mão/diagnóstico , Dermatoses da Mão/etiologia , Humanos , Japão , Masculino , Pessoa de Meia-Idade , Testes do Emplastro , Medição de Risco , Índice de Gravidade de Doença
4.
J Dermatol ; 32(8): 632-7, 2005 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16334862

RESUMO

We have treated two patients with extramammary Paget's disease/carcinoma (EMPD/C), a 62-year-old woman and a 78-year-old man. In both patients, lymph nodes in the areas of the bilateral inguinal, external iliac arteries, and abdominal aorta were affected. After surgery, they underwent 5 courses of systemic combination chemotherapy at 4-week intervals to residual or recurrent lymph node metastasis. Each course consisted of 3.5 mg mitomycin C and 50 mg epirubicin (day 1), 0.6 mg vincristine (days 1 and 7), 30 mg cisplatin (days 1, 2, and 3), and 350 mg 5-fluorouracil (days 3, 4, 5, 6, and 7). The affected lymph nodes in both patients subsided in response to the chemotherapy. Positron emission tomography (PET) scans confirmed the complete remission of lymph node metastasis in Case 1. In Case 2, they were reduced by more than 90% on computed tomography (CT) scans. Adverse effects included leukocytopenia, vomiting, hypesthesia, and constipation, all of which disappeared after the completion of chemotherapy. While surgery with wide local excision is the treatment of choice in patients with EMPD/C, there is currently no standardized treatment for advanced cases with metastasis. We describe two patients with EMPD/C whose metastatic lesions responded well to this combination of chemotherapy.


Assuntos
Doença de Paget Extramamária/diagnóstico , Neoplasias Cutâneas/diagnóstico , Idoso , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Terapia Combinada , Diagnóstico Diferencial , Feminino , Virilha , Humanos , Metástase Linfática , Masculino , Pessoa de Meia-Idade , Doença de Paget Extramamária/diagnóstico por imagem , Doença de Paget Extramamária/patologia , Doença de Paget Extramamária/terapia , Períneo , Neoplasias Cutâneas/diagnóstico por imagem , Neoplasias Cutâneas/patologia , Neoplasias Cutâneas/terapia , Tomografia Computadorizada por Raios X
5.
J Am Acad Dermatol ; 51(2 Suppl): S83-7, 2004 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-15280820

RESUMO

The painful orogenital ulcerations of Behçet's disease are among the major symptoms of patients and are often intractable. We assessed the efficacy of granulocyte and monocyte adsorption apheresis therapy in two patients, a 21-year-old man with orogenital ulcerations and a 50-year-old woman with genital ulceration and abdominal pain. They underwent 5 and 8 granulocyte and monocyte adsorption apheresis treatments at 5-day intervals, respectively. The painful orogenital ulcerations of the man responded dramatically and the genital ulcer of the woman decreased in size and her abdominal pain was improved. Our results demonstrate that granulocyte and monocyte adsorption apheresis may be useful for treating orogenital ulcerations of Behçet's disease.


Assuntos
Síndrome de Behçet/sangue , Síndrome de Behçet/terapia , Remoção de Componentes Sanguíneos/métodos , Antígeno de Macrófago 1/metabolismo , Adsorção , Adulto , Síndrome de Behçet/diagnóstico , Feminino , Citometria de Fluxo , Granulócitos/metabolismo , Humanos , Masculino , Pessoa de Meia-Idade , Monócitos/metabolismo , Neutrófilos/metabolismo , Medição da Dor , Indução de Remissão
6.
J Rheumatol ; 29(11): 2266-70, 2002 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-12415580

RESUMO

OBJECTIVE: To detect expression of the secreted frizzled related protein (sFRP) gene in synovial cells from patients with arthritis. METHODS: Expression of sFRP-1, 2, 3, 4, and 5 genes was detected in synovial cells from patients with rheumatoid arthritis (RA) and osteoarthritis (OA) by semiquantitative reverse transcription-polymerase chain reaction (RT-PCR) analysis. To identify synovial cell populations expressing sFRP-1, 3, and 4 genes, expression was compared in macrophage-rich populations and fibroblast-like cell-rich populations by RT-PCR. Levels of expression of these genes were also studied in activated peripheral blood mononuclear cells (PBMC) and activated skin fibroblasts. RESULTS: Expression of the sFRP-1, 3, and 4 genes was observed in both RA and OA synovial cells. sFRP-1 and 4 genes were expressed predominantly in fibroblast-like cell-rich populations, and the sFRP-3 gene was expressed predominantly in macrophage-rich populations. Levels of expression of sFRP-3 and 4 genes were elevated in activated PBMC and activated skin fibroblasts. CONCLUSION: Our findings suggest that sFRP-1, 3, and 4 may play different roles in the pathogenesis of synovitis.


Assuntos
Artrite/genética , Artrite/metabolismo , Proteínas/genética , Membrana Sinovial/metabolismo , Proteínas de Peixe-Zebra , Artrite/fisiopatologia , Artrite Reumatoide/genética , Artrite Reumatoide/metabolismo , Artrite Reumatoide/fisiopatologia , Células Cultivadas , Fibroblastos/metabolismo , Regulação da Expressão Gênica/fisiologia , Humanos , Peptídeos e Proteínas de Sinalização Intracelular , Macrófagos/metabolismo , Osteoartrite/genética , Osteoartrite/metabolismo , Osteoartrite/fisiopatologia , Proteínas Proto-Oncogênicas/genética , Proteínas Proto-Oncogênicas/metabolismo , Transdução de Sinais/genética , Membrana Sinovial/fisiopatologia , Proteínas Wnt
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