Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Añadir filtros








Tipo de estudio
Intervalo de año
1.
Urology Annals. 2015; 7 (2): 236-239
en Inglés | IMEMR | ID: emr-162376

RESUMEN

Primitive neuroectodermal tumor of the kidney is a rare tumor. A total of approximately 79 primary renal cases have been reported to date. Primitive neuroectodermal tumors occur preferentially in the soft-tissues of the paravertebral region and chest wall, less frequently in extremities, with a slight male predominance. We report a case of primitive neuroectodermal tumor of the kidney in a 17-year-old male with a pre-operative diagnosis of renal cell carcinoma-stage 4. The patient underwent radical nephrectomy and histopathological examination revealed a highly aggressive tumor of monotonous sheets of round cells with focal areas of rosette formations and high mitotic rate with Ki67 index of 25-30%. Tumor cells were positive for CD 99 confirming the diagnosis of primitive neuroectodermal tumor. Primitive neuroectodermal tumor of the kidney needs to be kept in mind as a differential diagnosis in young adults presenting with a large kidney mass

2.
Urology Annals. 2010; 2 (1): 36-38
en Inglés | IMEMR | ID: emr-97955

RESUMEN

We report and describe the presentation, pathological diagnosis with immunostaining and management of a rare case of capsular renal leiomyosarcoma encasing the inferior vena cava [IVC]. We have reviewed and tabulated other such similar cases. The present case was successfully managed by radical nephrectomy and adjuvant radio-chemotherapy. Immunostaining should be freely used to define the histological type of renal sarcoma in order to accurately counsel and deliver a prognosis for patients with renal leiomyosarcomas with a poor prognosis


Asunto(s)
Humanos , Femenino , Persona de Mediana Edad , Leiomiosarcoma/diagnóstico , Leiomiosarcoma/patología , Neoplasias Renales/diagnóstico , Inmunohistoquímica , Vena Cava Inferior
3.
Pakistan Journal of Pathology. 2009; 20 (2): 63-65
en Inglés | IMEMR | ID: emr-125566

RESUMEN

Chylous cysts of the mesentery are rare intra-abdominal masses in children. Very few cases are reported in the literature reviewed. Chylous cysts are rare variants of mesenteric lesions and constitute from 7.3% to 9.9% of all abdominal cysts. Present case showed a giant chylomesenteric cyst in a 10 year child complaining of abdominal distension since two years along with interesting finding of granulomatous inflammation in the adjoining jejunum in child, which is not yet reported in literature reviewed


Asunto(s)
Humanos , Masculino , Niño , Quilo , Quistes/diagnóstico , Mesenterio/patología , Quistes/cirugía
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA