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2012, Number 4

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Arch Neurocien 2012; 17 (4)

Prions: update and review of the handling of surgical brain biopsies

Hernández SM, Zarate-Méndez A, Ruiz y Cuéllar LE, Lucino-Castillo J, Lujan-Guerra J, Franco-Téllez JJ, Martínez-Escobar C, del Rio-Mendoza ED
Full text How to cite this article

Language: Spanish
References: 14
Page: 234-241
PDF size: 172.82 Kb.


Key words:

prions, encephalopathy, spongiform, biopsy.

ABSTRACT

Update the knowledge about particles called prions, handling precautions and recommendations of tissue in patients with suspected infection, in addition to a systematization of the item has slopes of great medical interest. We reviewed studies of the last 10 years systematically with keywords that included, prion, orCreutzfeldtdakob spongiform encephalopathy, dementia and brain biopsy progression fast. In Mesh Ime&line), human papers were included in English and Spanish domains. We perlormed a screening of the work that made mention of experience (more than onol and that related to the handling precautions and tissues of patients with spongiform encephalopathy. Consistent with the literature, patients with probable prion disease should be treated with great caution, first to see if there is possibility brain biopsy to confirm the diagnosis, and after his death according to European recommendations mainly in the preparation of cremation. The sporadic appearance of disease is spontaneous, the prion protein remains a major source of molecular research has generated two novel awards. Not everything has been linked to disease just as there are approaches that knowledge of the foundations of learning is linked to prions according to faculty experts like Professor Eric R. Kandel.


REFERENCES

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  2. Polo JM. The history and classification of human prion diseases. Rev Neurol 2000;31:137-41.

  3. Liberski PP, Brown P. Kuru: a half-opened window onto the landscape of neurodegenerative diseases. Folia Neuropathol 2004;42 Suppl A:3-14.

  4. Kristensson K, Winblad B. Nobel Prize to Stanley Prusiner for the discovery of prions. Ugeskr Laeger 1997;159:7645-9.

  5. Gasset M, Westaway D. Prions and their biology. Rev Neurol 2000;31:129-32.

  6. Stanley B. Prusiner Prions PNAS November 10, 1998;(95)23: 13363-83.

  7. Red de excelencia dedicada a la investigación en enfermedades priónicas [sobre los priones enfermedades priónicas o EETs] http://www.neuroprion.org/es/about-prion.html

  8. Serologicals Corporation Biotech Production Plant, Lawrence, KS, USA. A molecular model of a prion protein that causes BSE. http://www.pharmaceutical-technology.com/projects/ Serologicals/Serologicals5.html

  9. Zivkovic S, Boada M, López O. Revisión de la enfermedad del Creutzfeldt-Jakob y otras enfermedades prionicas. Rev Neurol 2000:31:1171-9.

  10. Cuellar Juan. Impor tancia para la Salud Pública de las encefalopatías espongiformes transmisibles: El mal de las “vacas locas”. Boletín Epidemiológico / OPS, 2001;(22), 1.

  11. The National Creutzfeldt-Jakob disease sur veillance unit (NCJDSU), www.cjd.ed.ac.uk

  12. Advisory Committee on Dangerous Pathogens (ACDP) ,TSE guidance, Guidance from the ACDP TSE Working Group, http:/ /www.dh.gov.uk, June 2003.

  13. Outline protocol for management of instruments and tissues from brain biopsy, procedures on patients with progressive neurological disorders, http://www.dh.gov.uk, Department of Health 2004.

  14. Hurley Robin A, Taber Katherine H. Windows to the brain. Insihgts froma Neuroimaging Ed. Ame Psych Publis, Inc. 2008.




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C?MO CITAR (Vancouver)

Arch Neurocien. 2012;17