Saturday, October 15, 2011

Neuropathological and Neuroradiological Spectrum of Pediatric Malignant Gliomas: Correlation With Ou

BACKGROUND: The diagnostic accuracy and reproducibility for glioma histological diagnosis are suboptimal. OBJECTIVE: To characterize radiological and histological features in pediatric malignant gliomas and to determine whether they had an impact on survival. METHODS: We retrospectively reviewed a series of 96 pediatric malignant gliomas. All histological samples were blindly and independently reviewed and classified according to World Health Organization 2007 and Sainte-Anne classifications. Radiological features were reviewed independently. Statistical analyses were performed to investigate the relationship between clinical, radiological, and histological features and survival. RESULTS: Cohort median age was 7.8 years; median follow-up was 4.8 years. Tumors involved cerebral hemispheres or basal ganglia in 82% of cases and brainstem in the remaining 18%. After histopathological review, low-grade gliomas and nonglial tumors were excluded (n = 27). The World Health Organization classification was not able to demonstrate differences between groups and patients survival. The Sainte-Anne classification identified a 3-year survival rate difference between the histological subgroups (oligodendroglioma A, oligodendroglioma B, malignant glioneuronal tumors, and glioblastomas; P = .02). The malignant glioneuronal tumor was the only glioma subtype with specific radiological features. Tumor location was significantly associated with 3-year survival rate (P = .005). Meningeal attachment was the only radiological criteria associated with longer survival (P = .02). CONCLUSION: The Sainte-Anne classification was better able to distinguish pediatric malignant gliomas in terms of survival compared with the World Health Organization classification. In this series, neither of these 2 histological classifications provided a prognostic stratification of the patients.





Multisession Radiosurgery for Optic Nerve Sheath Meningiomas—An Effective Option: Preliminary Resul

BACKGROUND: Traditional treatment options for optic nerve sheath meningiomas (ONSMs) include observation, surgery, and radiotherapy, but to date none of these has become the clear treatment of choice. OBJECTIVE: To evaluate the effectiveness and safety of multisession radiosurgery for ONSMs. METHODS: From May 2004 to June 2008, 21 patients with ONSMs were treated by radiosurgery using the frameless CyberKnife system. Patient age ranged from 36 to 73 years (mean, 54 years). All patients were treated using multisession radiosurgery, with 5 fractions of 5 Gy each to a total dose of 25 Gy prescribed to the 75% to 85% isodose line. Patients were evaluated for tumor growth control and visual function. RESULTS: The median pretreatment tumor volume was 2.8 mL (range, 0.3-23 mL). The mean follow-up was 30 months (range, 11-68 months). All patients tolerated treatment well, with only 1 patient in whom a mild optic neuropathy developed (which remitted after systemic steroid therapy). No other acute or late radiation-induced toxicities were observed. No patients showed ONSM progression on follow-up magnetic resonance imaging. Two patients (10%) had a partial response. No patients had worsening of visual function; visual function was stable in 65% and improved in 35% of patients. CONCLUSION: Multisession radiosurgery for ONSMs was found to be safe and effective. The preliminary results from this study, in terms of growth control, visual function improvement, and toxicity, are quite promising. Further investigations are warranted. ABBREVIATIONS: fSRT: fractionated stereotactic radiation therapy mSRS: multisession radiosurgery ONSM: optic nerve sheath meningioma





Corticosteroid-use in primary and secondary brain tumour patients: a review

Abstract  
Corticosteroids have been effective in the management of cerebral oedema, in the context of brain tumours, for many decades. Though their effectiveness is well-established, this needs to be balanced against their potential to cause significant side effects. There is currently little consensus in the literature about how this should be done. This article reviews the literature, specifically in relation to the role of corticosteroids in primary and secondary brain tumour patients. Areas reviewed include corticosteroid pharmacology, indications, mechanism of action, toxicity profile, prescribing practices, and corticosteroid-sparing agents.

  • Content Type Journal Article
  • Category Topic Review
  • Pages 1-11
  • DOI 10.1007/s11060-011-0713-3
  • Authors
    • Richella Ryan, Palliative Care Department, Elsworth House, Addenbrookes Hospital, Cambridge University Hospitals NHS Foundation Trust, Hills Road, Cambridge, CB2 0QQ UK
    • Sara Booth, Palliative Care Department, Elsworth House, Addenbrookes Hospital, Cambridge University Hospitals NHS Foundation Trust, Hills Road, Cambridge, CB2 0QQ UK
    • Stephen Price, University of Cambridge, Cambridge, UK





Friday, October 14, 2011

Ocular melanoma: Keep your eyes open for late brain metastases

Danilo O de A. Silva, Georgios K Matis, Leonardo F Costa, Matheus A. P Kitamura, Eduardo V de C. Júnior, Breno J A. P Barbosa, Isaac B Santiago, Tatiane I Silva, Fabiana Q de P. A. Silva, Carlos U Pereira, Hildo R C Azevedo Filho

Surgical Neurology International 2011 2(1):144-144

Background: The most frequent intraocular malignant tumor is choroidal melanoma (CM). Although brain metastasis is a common feature of other types of cancers, metastasis of CM to the brain is a rare entity. Case Description: The authors report a case of a 28-year-old woman presenting with a single brain metastasis, 10 years after the treatment of a CM. She underwent a total en-bloc resection of the lesion, and the diagnosis was confirmed histopathologically. The patient concomitantly received whole-brain irradiation therapy combined with chemotherapy, with a survival period of 24 months. Conclusion: The present case report draws attention to the necessity of a close and lifelong follow-up of patients treated for this malignancy. The international literature is also reviewed.







Júlio Leonardo B. Pereira
http://www.neurocirurgiabr.com
http://www.radiocirurgia.org

Ectopic pineal chordoma

Eberval G Figueiredo, Wagner M Tavares, Leonardo Welling, Sergio Rosemberg, Manoel Jacobsen Teixeira

Surgical Neurology International 2011 2(1):145-145

Background: Chordomas are rare tumors that arise from the remnants of embryonic notochord anywhere along the neuroaxis. Even though they may occur in an extraosseous intradural location, the most common sites include the sacrococcygeal and clivus regions. The authors report a unique presentation encompassing the pineal region with metastasis to the peritoneum after a ventriculoperitoneal (VP) shunt procedure and review the current knowledge about their pathophysiology and management. The presentation and clinical history endorse the idea that intradural extraosseous chordomas may be distinct from ecchordosis physaliphora and probably do not derive from it. Case Description: An 18-year-old male with previous history of VP shunt presented to the emergency room with pain and abdominal distension. Computed tomography (CT) scans revealed a mass in the pineal region and in the abdominal cavity. Histopathologic exams showed chordoma in both abdominal and cranial samples. The patient died due to systemic complications. Conclusion: The authors hypothesized that notochord remnants may subsist within the brain and occasionally may generate a neoplastic lesion.







Júlio Leonardo B. Pereira
http://www.neurocirurgiabr.com
http://www.radiocirurgia.org

Targeting Brain Cancer Stem Cells, New Screening Strategy

According to a new study, published in the October issue of Molecular Cancer Therapeutics, a peer-reviewed journal of the American Association of Cancer Research, stem cells responsible for creating deadly brain tumors can be identified and characterized by chemical compounds that can target the stem cells...







Júlio Leonardo B. Pereira
http://www.neurocirurgiabr.com
http://www.radiocirurgia.org

Ahead of Print: Importance of Preserved Periosteum Around Jugular Foramen Neurinomas for Functional

Full article access for Neurosurgery subscribers at Neurosurgery-Online.com.

BACKGROUND: Surgical removal of jugular foramen (JF) neurinomas remains controversial due to their radicality in relation to periosteal sheath structures.

OBJECTIVE: To clarify the particular meningeal structures of the JF with the aim of helping to eliminate surgical complications of the lower cranial nerves (LCNs).

METHODS: We sectioned 6 JFs and examined histological sections using Masson's trichrome stain. A consecutive series of 25 patients with JF neurinomas was also analyzed, and the MIB-1 index of each excised tumor was determined.

RESULTS: In the JF, meningeal dura disappeared at the nerve entrance, forming a jugular pocket. JF neurinomas were classified into 4 types: subarachnoid (type A by Samii's classification), foraminal (type B), epidural (type C), and epi-subdural (type D). After an average follow-up of 9.2 years, tumors recurred in 9 cases (36%). Type A tumors did not show regrowth, unlike type B tumors, in which all recurred. Radical surgery by modified Fisch approach did not contribute to tumor radicality in types C and D tumors, even in cases where LCN function was sacrificed. In preserved periosteum, postoperative LCN deterioration was decreased. Bivariate correlation analysis revealed that jugular pocket extension, tumor removal, MIB-1 >3%, and reoperation or gamma knife use were significant recurrence factors.

CONCLUSION: For LCN preservation, the periosteal layer covering the cranial nerves must be left intact except in patients with subarachnoid tumor type. To prevent tumor regrowth, postoperative gamma knife treatment is recommended in tumors with an MIB-1 >3%.

Full article access for Neurosurgery subscribers at Neurosurgery-Online.com.









Júlio Leonardo B. Pereira
http://www.neurocirurgiabr.com
http://www.radiocirurgia.org

Conflicts of Interest Abound in Diabetes Guidelines Committees

An investigation into the potential conflicts of interest among members of diabetes and hyperlipidemia guideline-writing committees reveals that growing concerns about industry's influence on clinical practice may be well-founded.
Heartwire







Júlio Leonardo B. Pereira
http://www.neurocirurgiabr.com
http://www.radiocirurgia.org

Sunday, September 4, 2011

Malformações arteriovenosas

Malformações Arteriovenosas

A malformações arteriovenosas são anormalidades vasculares devido a comunicações entre veias e artérias sem um leito capilar adequado. São consideradas anormalidades congênitas mas podem também se desenvolver no desenvolvimento. 

A apresentação clinica da MAV se deve por sangramento intracraniano e crises convulsivas.  A chance de uma MAV sangrar é de 2-4% ao ano mas com uma morbidade de quase 30% e  mortalidade de 10%.
Os exames para o diagnóstico devem ser uma RNM de encéfalo e angiografia de vasos cerebrais. A graduação da MAV deve ser realizada pela escala abaixo:


 

 

GRADUAÇÃO DE SPETZLER-MARTIN PARA  MAV

 

Tamanho

Pequeno (< 3cm)=1  Médio (3-6cm)=2 Grande (> 6cm) =3

Eloqüência do cérebro adjacente

Não-eloqüente=0  Eloqüente =1

Drenagem venosa

Somente superficial= 0 Profunda =1

 

Sendo classificada de grau 1 a 5.

O tratamento de escolha para uma MAV é quando possível cirúrgico. Sendo necessário uma avaliação com uma equipe composta de Neurocirurgião especializado em Vascular, Endovascular e Radiocirurgia para individualizar e analisar cada caso. 

A radiocirurgia estereotáxica tem se mostrado bastante efetiva para MAV pequenas (menores de 3 cm) sendo também utilizada em lesões profundas com difícil abordagem cirúrgica. Outros aplicações da radiocirurgia nas MAV tem sido fruto de diversos trabalhos científicos e com bons resultados.

Alguns temas sobre radiocirurgia que ainda não possuem evidência definitiva sendo necessário discutir cada caso individualmente.

Caso você seja profissional de saúde ou deseje saber mais sobre esse tema, existem diversos artigos. Sugiro mais informações no Blog Radiocirurgia sub-tema MAV

Referências:

1. Practical Handbook of Neurosurgery From Leading Neurosurgeons Sindou, Marc (Ed.)

 

AVISO: A medicina é uma área em constante mudança. Os autores procuraram fornecer informação que seja correcta e completa à data da publicação. Contudo, atendendo às rápidas alterações que ocorrem na ciência médica e do mesmo modo à possibilidade do erro humano, este sítio pode conter inexactidões técnicas, tipográficas ou outros erros.


Por Júlio Leonardo Barbosa Pereira

www.radiocirurgia.com.br