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1.
Balkan Med J ; 37(5): 287-290, 2020 08 11.
Artigo em Inglês | MEDLINE | ID: mdl-32441904

RESUMO

Aims: Juxtaglomerular cell tumor is a rare kidney tumor. This study aimed to report the clinic features of juxtaglomerular cell tumor and our treatment experience. Methods: The medical records of 9 juxtaglomerular cell tumor patients treated in our hospital from 1997 to 2017 were retrospectively reviewed. Clinical characteristics, immunohistochemical findings, treatments and outcomes were collected. Results: The mean age of 9 patients was 24±8.1 years (range: 18-37). All cases had symptoms of hypertension, hyperaldosteronism, high plasma renin, high plasma angiotensin II. Four cases had hypokalemia. The renal masses were found by enhanced contrast tomography in all patients. One case received ultrasound-guided ablation and was clinically diagnosed with juxtaglomerular cell tumor. Among the remaining 8 cases, 2 cases received nephrectomy while 6 underwent partial nephrectomy. The 8 cases were pathologically diagnosed with juxtaglomerular cell tumor. Immunohistochemical findings showed that juxtaglomerular cell tumor was positive for vimentin, CD34, and actin but negative for chromogranin A. After treatment, all the patients had normal levels of blood pressure, serum renin activity, potassium, and aldosterone. No patients had tumor progress or metastasis within a median follow-up period of 94 (range: 33-241) months. Conclusion: Hypertension combined with hyperaldosteronism and hypokalemia secondary to high plasma renin activity are the typical symptoms of juxtaglomerular cell tumor. Partial nephrectomy is an optimal treatment for juxtaglomerular cell tumor.


Assuntos
Osteossarcoma Justacortical/classificação , Adolescente , Adulto , Gerenciamento Clínico , Feminino , Humanos , Masculino , Nefrectomia/métodos , Osteossarcoma Justacortical/fisiopatologia , Estudos Retrospectivos , Tomografia Computadorizada por Raios X/métodos , Ultrassonografia de Intervenção/métodos
2.
JBR-BTR ; 88(4): 204-8, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-16176080

RESUMO

The purpose of this brief review is to give an overview of the different imaging features of the various types of osteosarcoma, based on their macroscopic location within the musculoskeletal system. Further subdivision can be made by histological criteria and/or more specific location. Standard radiographic features allowing their differentiation will be highlighted. The value of cross-sectional imaging in the pre-operative staging, assessment of local extension, monitoring of response to treatment and guiding biopsy will be emphasized as well.


Assuntos
Neoplasias Ósseas/diagnóstico , Diagnóstico por Imagem , Osteossarcoma Justacortical/diagnóstico , Osteossarcoma/diagnóstico , Neoplasias Ósseas/classificação , Humanos , Osteossarcoma/classificação , Osteossarcoma Justacortical/classificação
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