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1.
BMJ Case Rep ; 17(3)2024 Mar 19.
Artigo em Inglês | MEDLINE | ID: mdl-38508596

RESUMO

We report a case of a mid-20s primigravida at 37 weeks' gestation who presented with severe headache and acute neurological deterioration. The CT brain scan showed hydrocephalus caused by a colloid cyst in the third ventricle. The patient underwent emergency placement of an external ventricular drain for decompression of acute hydrocephalus. Four hours later, labour commenced spontaneously, and in view of her neurological status, a decision was taken to perform a caesarean section under general anaesthetics. Four days postpartum, the patient underwent an endoscopic removal of the cyst. Intracranial emergencies during pregnancy are rare and challenging to manage. The mortality rate can be significant. Diagnostic and surgical intervention should not be delayed because of pregnancy. An individualised treatment approach is required with multidisciplinary input. The collaborative efforts of our multidisciplinary team resulted in prompt diagnosis and surgical treatment in this case that resulted in both a healthy mother and child.


Assuntos
Cistos Coloides , Hidrocefalia , Trabalho de Parto , Terceiro Ventrículo , Criança , Humanos , Gravidez , Feminino , Cesárea , Hidrocefalia/etiologia , Hidrocefalia/cirurgia , Terceiro Ventrículo/cirurgia
2.
J Clin Neurosci ; 19(8): 1170-1, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22658242

RESUMO

Intracranial mesenchymal chondrosarcoma is a rare, high-grade malignancy with the highest prevalence in young adults. Because of its rarity, most data regarding survival are limited to case studies and small series. We present a 71-year-old woman with an intracranial dural based mesenchymal chondrosarcoma located in the anterior skull base, to our knowledge the oldest patient reported with this tumor.


Assuntos
Neoplasias Ósseas/diagnóstico , Condrossarcoma Mesenquimal/diagnóstico , Dura-Máter/patologia , Idoso , Feminino , Humanos , Imageamento por Ressonância Magnética , Proteínas S100/metabolismo , Base do Crânio/patologia
3.
Emerg Med J ; 24(10): 707-9, 2007 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-17901272

RESUMO

BACKGROUND: To perform a risk analysis study to determine the probability of a spinal fracture being of malignant origin in patients presenting at a level I trauma centre emergency room after trauma. PATIENTS AND METHODS: Data from 334 consecutive patients were retrospectively obtained from 1993 to 2003. They were divided into two groups: group 1--(benign) traumatic fractures; and group 2--malignant fractures (n = 32). For statistical analysis independent Student t test, chi2 test, and backward-stepwise logistic regression were used. RESULTS: The risk of vertebral fractures appearing to be of malignant origin increased with anatomical location (non-cervical--that is, thoracic or lumbar: odds ratio (OR) 48, 95% confidence interval (CI) 8 to 291), a history of malignancy (OR 72, 95% CI 12 to 422), trauma mechanism (that is, high energy: OR 0.03, 95% CI 0.003 to 0.28), and age >64 years (OR 3, 95% CI 0.9 to 12). Hence, patients over 64 years old attending the emergency room, with a vertebral fracture after a low energy trauma, had an approximately 50% chance of having a malignant fracture. With a non-cervical location and a history of malignancy this increased to 98%. Regardless of the trauma mechanism and age of the patient, a history of a malignancy and a non-cervical fracture posed at least a 36% risk of having a malignant fracture. CONCLUSION: Supported by the present results we feel the probability of malignant fractures, although not frequently encountered, should always be considered in elderly and middle-aged patients with a history of malignancy and a non-cervical traumatic fracture.


Assuntos
Neoplasias Ósseas/epidemiologia , Serviço Hospitalar de Emergência/estatística & dados numéricos , Fraturas Espontâneas/epidemiologia , Fraturas da Coluna Vertebral/epidemiologia , Acidentes por Quedas/estatística & dados numéricos , Acidentes de Trânsito/estatística & dados numéricos , Adulto , Distribuição por Idade , Estudos de Casos e Controles , Causalidade , Comorbidade , Feminino , Humanos , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Países Baixos/epidemiologia , Prevalência , Estudos Retrospectivos , Fatores de Risco , Distribuição por Sexo
4.
J Neurosurg ; 97(6): 1390-6, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12507138

RESUMO

OBJECT: Diagnosing primary central nervous system lymphoma (PCNSL) may be difficult either because of a paucity of tumor cells in the brain biopsy specimens or a failure to demonstrate monoclonality on immunomorphological studies. Monoclonality can also be demonstrated by amplification of the rearranged immunoglobulin H genes by polymerase chain reaction (PCR) to the framework region (FR)3 and FR2 complementarity determining region (CDR)-III and CDR-II of these genes. The PCR method is feasible with formalin-fixed, paraffin-embedded biopsy material and has proven to be helpful in the diagnosis of non-Hodgkin lymphoma on biopsy samples obtained from various locations in the body. Nevertheless, few studies have addressed the value of this method in the context of PCNSL. In the present study, the contribution of both FR3 single and FR2 seminested PCR procedures for confirming the diagnosis of PCNSL was estimated retrospectively in 30 cases of PCNSL and in three cases of epidural lymphoma. METHODS: Twenty-eight cases of immunophenotypically confirmed PCNSL and two of suspected lymphoma were studied. Tissue specimens obtained in 22 cases of other cerebral diseases, among which were various inflammatory conditions. were used as negative controls. In 18 (60%) of 30 cases the results of FR3 PCR demonstrated monoclonality, whereas FR2 PCR showed monoclonality in 12 cases (40%). In 11 cases FR3 PCR yielded monoclonal patterns and FR2 PCR did not, whereas reversibly in five cases FR2 PCR proved monoclonality and FR3 PCR failed to do so. Adding the results of FR3 to those of FR2 PCR, monoclonal patterns were obtained in 23 (77%) of 30 cases. In both cases in which lymphoma was suspected but not proven immunomorphologically, FR3 PCR revealed monoclonality, as did FR2 PCR in one case. In all 22 control lesions either polyclonal patterns were seen or no consistent patterns were obtained. In the PCNSL group, older age of patients and multifocal presentation of lesions on neuroimaging were significantly associated with worse survival. No correlation between histological subtype and clinical outcome was elucidated. CONCLUSIONS: The application of FR3 and FR2 PCR is a useful additional tool in making the diagnosis of PCNSL. Moreover, in some cases the PCR method may be essential in distinguishing neoplasia from reactive conditions.


Assuntos
Neoplasias do Sistema Nervoso Central/genética , Rearranjo Gênico , Imunoglobulinas/genética , Linfoma não Hodgkin/genética , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Biópsia , Neoplasias do Sistema Nervoso Central/mortalidade , Neoplasias do Sistema Nervoso Central/patologia , Feminino , Humanos , Linfoma não Hodgkin/mortalidade , Linfoma não Hodgkin/patologia , Masculino , Pessoa de Meia-Idade , Reação em Cadeia da Polimerase , Estudos Retrospectivos , Análise de Sobrevida
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