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6.
Pediatr Neurosurg ; 52(3): 173-180, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28222441

RESUMO

Desmoplastic infantile gliomas are rare, benign tumors of the early infancy period. Two histological subtypes - desmoplastic infantile astrocytoma (DIA) and desmoplastic infantile ganglioglioma - have been described. The characteristic features of DIAs are lobar location, glial histology, and excellent prognosis after complete surgical excision. DIAs usually present as solitary, cortical-surfacing, solid-cystic neoplasms; however, atypical, aggressive, and multifocal variants of DIA have been reported in the literature. These rare DIAs presenting with multiple lesions pose a diagnostic as well as a therapeutic dilemma. We report an unusual case of an 8-month-old female infant diagnosed with multifocal (cranial and spinal) DIA and obstructive hydrocephalus and discuss the radiological and histological features of this rare variant of DIA. The patient underwent ventriculoperitoneal shunt placement to relieve the hydrocephalus, excisional biopsy from a surfacing lesion in the right frontal lobe, and multiple cycles of chemotherapy; however, the lesions continued to progress, and the patient is likely to have an unfavorable outcome.


Assuntos
Astrocitoma , Neoplasias Encefálicas/patologia , Ganglioglioma/patologia , Astrocitoma/complicações , Astrocitoma/patologia , Feminino , Humanos , Hidrocefalia/etiologia , Hidrocefalia/cirurgia , Lactente , Imageamento por Ressonância Magnética , Coluna Vertebral/patologia , Derivação Ventriculoperitoneal
7.
Cancer Genet Cytogenet ; 141(1): 14-9, 2003 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-12581893

RESUMO

Cytogenetic analysis of fine needle aspiration cultures was performed on 189 patients with non-Hodgkin lymphoma from South India. Successful karyotyping was possible in 97 patients (51.3%). Burkitt lymphoma constituted 56% of the cases studied followed by diffuse type 20%, follicular 8.8%, lymphoblastic 6.6%, and unclassified 6.6%. Characteristic chromosomal translocations were t(8;14)(q24;q32) [32.2%], t(8;22)(q24;q11) [10%], t(2;8)(p12;q24) [2.2%], t(14;18)(q34;q21) [3.3%], and t(11;14)(q23;q32) [2.2%]. Notable geographical variation of some structural abnormalities was the finding in the present study such as, lower frequency of t(14;18) in follicular lymphomas and higher frequency of t(8;14) in Burkitt lymphomas when compared with the Western studies.


Assuntos
Aberrações Cromossômicas , Linfoma não Hodgkin/epidemiologia , Linfoma não Hodgkin/genética , Adolescente , Adulto , Idoso , Linfoma de Burkitt/epidemiologia , Linfoma de Burkitt/genética , Criança , Pré-Escolar , Feminino , Humanos , Índia/epidemiologia , Cariotipagem , Leucemia Linfoide/epidemiologia , Leucemia Linfoide/genética , Linfoma Folicular/epidemiologia , Linfoma Folicular/genética , Masculino , Pessoa de Meia-Idade
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