Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros

Base de dados
Tipo de documento
Intervalo de ano de publicação
1.
Childs Nerv Syst ; 40(1): 11-17, 2024 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-37819507

RESUMO

Raine's syndrome (RS) is a rare genetic disorder. Only 25 cases are in literature. Occurs due to genetic mutation resulting in deranged bone metabolism. Few cases are reported discussing the neurosurgical ramifications of the disease. We report a child diagnosed with RS. He was presented with multisutural synostosis requiring craniofacial intervention with two vault expansions. Additionally, required VP shunt due to hydrocephalus. We consider our case unique among reports of RS, as our patient has survived for 10. He died due to valve obstruction of the VP shunt. We also present a review of relevant medical literature.


Assuntos
Craniossinostoses , Hidrocefalia , Sinostose , Criança , Humanos , Masculino , Craniossinostoses/cirurgia , Hidrocefalia/etiologia , Hidrocefalia/cirurgia , Doenças Raras/cirurgia , Síndrome , Sinostose/cirurgia , Derivação Ventriculoperitoneal
2.
Surg Neurol Int ; 13: 572, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36600759

RESUMO

Background: A postoperative discal/annular cyst following lumbar discectomy may reproduce the symptoms/signs of a recurrent lumbar disc herniation (i.e., back pain and radiculopathy). Case Description: A 21-year-old rugby player developed leg pain after an uncomplicated lumbar microdiscectomy. The repeat lumbar magnetic resonance imaging confirmed a postoperative lumbar annular/ discal cyst, for which he underwent repeat surgery. The diagnosis was further confirmed histopathologically at surgery. Conclusion: Although rare, postoperative discal/annular cysts may be potential causes of recurrent postoperative pain and lumbar radiculopathy mimicking recurrent disc herniations.

3.
BMJ Case Rep ; 20152015 Mar 27.
Artigo em Inglês | MEDLINE | ID: mdl-25819823

RESUMO

A 20-year-old woman with a functioning ventriculoperitoneal (VP) shunt consistently reported unbearable vertex headaches and nausea during the last hour of her haemodialysis (HD) sessions. After one particularly severe episode, which was associated with vomiting, restlessness and blurred vision, her team suspected that she was developing dialysis disequilibrium syndrome. She improved fully on cessation of HD, requiring simple analgaesia only, and continued dialysis three times per week. Several more distressing episodes of nausea and headaches compelled us to give intravenous mannitol during HD, resulting in temporary improvement. Subsequently, shorter and more frequent dialysis sessions along with intravenous mannitol resulted in satisfactory clinical response.


Assuntos
Cefaleia/etiologia , Diálise Renal/efeitos adversos , Derivação Ventriculoperitoneal , Diuréticos Osmóticos/uso terapêutico , Feminino , Cefaleia/tratamento farmacológico , Humanos , Manitol/uso terapêutico , Náusea/etiologia , Diálise Renal/métodos , Transtornos da Visão/etiologia , Vômito/etiologia , Adulto Jovem
4.
J Clin Microbiol ; 47(5): 1599-601, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19261780

RESUMO

We describe two cases of Clostridium glycolicum wound infections in immunocompetent adults. The bacterium was identified by 16S rRNA gene sequencing. This is the third published report of the recovery of this organism from human clinical material and highlights the importance of the organism as a potential human pathogen. Our report extends the spectrum of the diseases caused by C. glycolicum.


Assuntos
Infecções por Clostridium/diagnóstico , Clostridium/isolamento & purificação , Infecção dos Ferimentos/microbiologia , Adulto , Infecções por Clostridium/microbiologia , DNA Bacteriano/genética , DNA Ribossômico/genética , Feminino , Humanos , Masculino , RNA Ribossômico 16S/genética , Análise de Sequência de DNA , Adulto Jovem
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA