Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Adicionar filtros








Intervalo de ano
1.
Korean Journal of Nephrology ; : 648-652, 2009.
Artigo em Coreano | WPRIM | ID: wpr-66068

RESUMO

C1q nephropathy is an immune complex glomerulonephritis defined by the presence of mesangial immunoglobins and complement deposits, most notably C1q, and the absence of clinical and laboratory evidence of systemic lupus erythematosus. Most patients with C1q nephropathy present nephrotic-range proteinuria, which has a poor response to steroid. Some patients may experience decreased renal function and progress to end stage renal disease. A 27year-old man presented with proteinuria and decreased mental state. The patient was hypertensive, with a blood pressure of 180/120 mmHg. Serum BUN/creatine was 18/1.8 mg/dL, and urinalysis revealed proteinuria (3+). Brain computed tomography showed right basal ganglial and intraventricular hemorrhage. The patient was treated with craniotomy and hematoma removal, and he also received carvedilol, losartan, nifedipine, and doxazosin for control of BP. Although his mental status recovered and blood pressure was controlled, the patient still showed subnephrotic proteinuria; therefore, renal biopsy was performed. Kidney biopsy showed segmental sclerosis in 3 out of 14 glomeruli, and mesangial C1q immunofluorescence positive staining. Electron microscopic findings revealed electron-dense deposits in the mesangium. The patient was treated with oral prednisolone, and proteinuria was alleviated after 8 weeks and remains in complete remission.


Assuntos
Humanos , Complexo Antígeno-Anticorpo , Biópsia , Pressão Sanguínea , Encéfalo , Carbazóis , Complemento C1q , Proteínas do Sistema Complemento , Craniotomia , Doxazossina , Elétrons , Imunofluorescência , Glomerulonefrite , Glomerulosclerose Segmentar e Focal , Hematoma , Hemorragia , Rim , Falência Renal Crônica , Losartan , Lúpus Eritematoso Sistêmico , Nifedipino , Prednisolona , Propanolaminas , Proteinúria , Esclerose , Urinálise
2.
Korean Journal of Dermatology ; : 1054-1056, 2004.
Artigo em Coreano | WPRIM | ID: wpr-112387

RESUMO

Transposition of the island pedicle flap is a versatile method of mobilizing tissue from a relatively distant reservoir and moving it across intervening tissue. Advantages are the similar color and texture to those of the affected area, the minimal donor scar, the increased viability with local blood supply, and the potential to camouflage scars into natural skin lines or cosmetic units. In a 73-year-old woman, the lesion of a basal cell carcinoma on her left nasal ala was removed by Mohs micrographic surgery and the resultant defect was reconstructed by transposition of the island pedicle flap. In our case, there were no significant complications and the final result was satisfactory in both functional and cosmetic aspects. Through our experience, we can confirm that transposition of the island pedicle flap is another alternative for the reconstruction of nasal alar defects.


Assuntos
Idoso , Feminino , Humanos , Carcinoma Basocelular , Cicatriz , Cirurgia de Mohs , Pele , Doadores de Tecidos
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA