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2.
Clin Biochem ; 18(3): 180-3, 1985 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-3888445

RESUMO

Beta 2-microglobulin levels were determined in the cerebrospinal fluid (CSF) of 119 children (ages 1 1/2 to 18 years) with malignant conditions; 87 with acute lymphoblastic leukemia, 9 with acute myeloblastic leukemia, 15 with lymphoma, and 8 with solid tumours. A total of 491 CSF specimens and 202 serum specimens were analyzed over a 12-month period. The mean CSF beta 2-microglobulin and serum beta 2-microglobulin were 1.11 +/- 0.58 mg/L and 1.5 +/- 0.64 mg/L respectively and were not different from the mean CSF (1.20 +/- 0.45 mg/L) and serum beta 2-microglobulin levels (1.70 +/- 0.45 mg/L) found in control patients. Meningeal leukemia was diagnosed on the basis of cytology in 7 patients. No elevation of CSF beta 2-microglobulin was found in any specimen at the time of CNS disease. Eleven other patients showed a transient rise in CSF beta 2-microglobulin above the reference range (greater than 2.1 mg/L). No evidence of CNS involvement was found in any of these patients. Five of these patients had received a combination of intrathecal methotrexate and irradiation therapy within the previous 4 months. A transient rise in CSF beta 2-microglobulin (2-3-fold increase over baseline CSF levels), which did not exceed the upper limit of the reference range was seen in 5 of 7 other children receiving the above therapy. Our study fails to demonstrate the usefulness of CSF beta 2-microglobulin for the diagnosis of CNS metastases but suggests that a transient elevation of CSF beta 2-microglobulin may occur after intrathecal methotrexate and irradiation therapy.


Assuntos
Leucemia/líquido cefalorraquidiano , Linfoma/líquido cefalorraquidiano , Microglobulina beta-2/líquido cefalorraquidiano , Adolescente , Neoplasias Encefálicas/diagnóstico , Neoplasias Encefálicas/secundário , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Masculino , Metotrexato/uso terapêutico
3.
Arch Dis Child ; 53(10): 822-4, 1978 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-215089

RESUMO

Retrospective radiological documentation of a growing Wilms's tumour in rare. Considered to be a relatively rapidly growing tumour, we present a case where there was adequate radiological evidence of a Wilms's tumour 4 years before the clinical metastatic presentation.


Assuntos
Neoplasias Renais/diagnóstico por imagem , Tumor de Wilms/diagnóstico por imagem , Adolescente , Feminino , Humanos , Neoplasias Renais/patologia , Radiografia , Tumor de Wilms/patologia
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