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1.
Pan Afr Med J ; 24: 64, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27642405

RESUMO

We report a rare case of an elderly woman presented with right renal mass with invasion of renal vein and several small lymphadenopathy in the hilar area. The diagnosis of kidney cancer is suspected and the patient underwent open radical nephrectomy, surrenalectomy and lymphadenectomy dissection. The pathologic examinations find a rosai dorfman disease. This unusual benign entity is uncommon in the kidney, but in medical imaging, it may simulate an infiltrative renal neoplasm, especially a lymphoma or leukemia or even renal cell carcinoma. A comprehensive literature review was undertaken to summarize the clinical and pathologic features of this disorder.


Assuntos
Histiocitose Sinusal/diagnóstico , Neoplasias Renais/diagnóstico , Nefrectomia/métodos , Idoso , Feminino , Histiocitose Sinusal/patologia , Histiocitose Sinusal/cirurgia , Humanos , Excisão de Linfonodo/métodos , Linfadenopatia/diagnóstico , Linfadenopatia/cirurgia
2.
J Med Case Rep ; 8: 465, 2014 Dec 26.
Artigo em Inglês | MEDLINE | ID: mdl-25541096

RESUMO

INTRODUCTION: A granular cell tumor involving the breast parenchyma was first described by Abrikossoff in 1931. Localization of this lesion to the breast is very rare, accounting for between 5% and 15% of all granular cell tumor cases. We present this case because of the rarity of this tumor. It is frequently confused with breast carcinoma on clinical and radiological examination, and its diagnosis can therefore be challenging for clinicians, radiologists and pathologists. CASE PRESENTATION: We report the case of a 32-year-old Moroccan woman who presented with a palpable mass in her right breast. Mammography and ultrasound examination revealed a heterogeneous, irregular and poorly limited mass, located at the union of the outer quadrants of her right breast. The mass was in contact with her latissimus dorsi and suspicious for malignancy. A histological examination combined with immunohistochemical study revealed it to be a granular cell tumor. CONCLUSION: Although a granular cell tumor of the breast is a rare breast neoplasm, it should be considered in the differential diagnosis of benign and malignant lesions. Pathologists should bear in mind a granular cell tumor when examining material containing cells with abundant granular cytoplasm to avoid misdiagnosing breast carcinoma, which could lead to unnecessary surgery.


Assuntos
Neoplasias da Mama/patologia , Tumor de Células Granulares/patologia , Mamografia , Ultrassonografia Mamária , Adulto , Neoplasias da Mama/cirurgia , Diagnóstico Diferencial , Feminino , Tumor de Células Granulares/cirurgia , Humanos , Imuno-Histoquímica , Resultado do Tratamento , Procedimentos Desnecessários
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