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1.
Artigo | IMSEAR | ID: sea-222100

RESUMO

Strategies to improve medication safety focused on acute care settings. Twenty-six studies and descriptions of quality improvement projects were identified. Strategies used to focus on recommendations to prevent medication errors at various stages, from a nationwide voluntary organization to improve safety of patients and empower education system of nurses and other health care providers in safe practices in health care system and vast growing technology.

4.
Artigo em Inglês | IMSEAR | ID: sea-87589

RESUMO

Visceral manifestations of von Hippel-Lindau disease (VHLD) are generally asymptomatic and their early detection is of considerable help in the management. This communication documents the usefulness of imaging studies in detecting visceral manifestations in two cases of VHLD.


Assuntos
Adulto , Carcinoma de Células Renais/diagnóstico , Humanos , Masculino , Feocromocitoma/diagnóstico , Tomografia Computadorizada por Raios X , Doença de von Hippel-Lindau/diagnóstico
5.
Neurol India ; 2004 Sep; 52(3): 384-6
Artigo em Inglês | IMSEAR | ID: sea-121694

RESUMO

Desmoplastic infantile ganglioglioma is a very rare supratentorial tumor occurring in the first two years of life. A five-month-old female infant presented with recurrent seizures, large head and loss of acquired milestones. Computerized Tomographic Scan of brain showed a large subarachnoid cyst with a solid intensely contrast enhancing tumor in the right temporoparietal region with severe degree of mass effect. Craniotomy and total excision of the tumor followed subsequently by subduro-peritoneal shunt for the extracerebral fluid collection was done. The child made good recovery. Histopathology revealed features of desmoplastic infantile ganglioglioma, viz., marked desmoplastic component with glial and neuronal elements. Immunohistochemistry showed positive staining for glial fibrillary acidic protein (GFAP) with areas of synaptophysin and chromogranin positivity. Desmoplastic infantile ganglioglioma is a rare tumor of infancy, which has excellent prognosis after total excision. No adjuvant therapy is required. This is the first Indian report of desmoplastic infantile ganglioglioma out of less than fifty cases reported worldwide.


Assuntos
Astrócitos/patologia , Neoplasias Encefálicas/patologia , Feminino , Ganglioglioma/patologia , Humanos , Lactente , Procedimentos Neurocirúrgicos , Convulsões/etiologia , Tomografia Computadorizada por Raios X
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