Compressive myelopathy secondary to spinal neurocysticercosis stablished by polymerase chain reaction

Luis Mario Piedra Bravo; Nelson López-Aguilera; Doménica Alejandra Figueroa-Martínez; Elsa Mishel Molina-Pinos; Xavier Merchán-del Hierro

doi:10.1016/j.neuarg.2018.03.002

Compressive myelopathy secondary to spinal neurocysticercosis stablished by polymerase chain reaction

Título traducido de la contribución: Mielopatía compresiva secundaria a neurocisticercosis espinal documentada por reacción en cadena de polimerasa

Luis Mario Piedra Bravo
, Nelson López-Aguilera
, Doménica Alejandra Figueroa-Martínez
, Elsa Mishel Molina-Pinos
, Xavier Merchán-del Hierro

Producción científica: Contribución a una revista › Artículo › revisión exhaustiva

Resumen

Neurocysticercosis is an endemic parasitic disease in several regions of the world. The spinal form is rare and its diagnosis is complex due to the clinical variability and the poor performance of the available additional tests. In this paper, we describe the case of a 34-year-old male patient who presented compressive myelopathy secondary to spinal neurocysticercosis confirmed by polymerase chain reaction and histopathology report. The patient was successfully treated with decompressive surgery. We discuss the clinical aspects, the usefulness of diagnostic tools —including polymerase chain reaction—, and the therapeutic options available for the treatment of spinal neurocysticercosis.

Título traducido de la contribución	Mielopatía compresiva secundaria a neurocisticercosis espinal documentada por reacción en cadena de polimerasa
Idioma original	Inglés
Páginas (desde-hasta)	96-100
Número de páginas	5
Publicación	Neurologia Argentina
Volumen	11
N.º	2
DOI	https://doi.org/10.1016/j.neuarg.2018.03.002
Estado	Publicada - 1 abr. 2019

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10.1016/j.neuarg.2018.03.002

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title = "Compressive myelopathy secondary to spinal neurocysticercosis stablished by polymerase chain reaction",

abstract = "Neurocysticercosis is an endemic parasitic disease in several regions of the world. The spinal form is rare and its diagnosis is complex due to the clinical variability and the poor performance of the available additional tests. In this paper, we describe the case of a 34-year-old male patient who presented compressive myelopathy secondary to spinal neurocysticercosis confirmed by polymerase chain reaction and histopathology report. The patient was successfully treated with decompressive surgery. We discuss the clinical aspects, the usefulness of diagnostic tools —including polymerase chain reaction—, and the therapeutic options available for the treatment of spinal neurocysticercosis.",

keywords = "Neurocysticercosis, Polymerase chain reaction, Spinal cord",

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note = "Publisher Copyright: {\textcopyright} 2018 Sociedad Neurol{\'o}gica Argentina",

year = "2019",

month = apr,

day = "1",

doi = "10.1016/j.neuarg.2018.03.002",

language = "Ingl{\'e}s",

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TY - JOUR

T1 - Compressive myelopathy secondary to spinal neurocysticercosis stablished by polymerase chain reaction

AU - Piedra Bravo, Luis Mario

AU - López-Aguilera, Nelson

AU - Figueroa-Martínez, Doménica Alejandra

AU - Molina-Pinos, Elsa Mishel

AU - Merchán-del Hierro, Xavier

PY - 2019/4/1

Y1 - 2019/4/1

N2 - Neurocysticercosis is an endemic parasitic disease in several regions of the world. The spinal form is rare and its diagnosis is complex due to the clinical variability and the poor performance of the available additional tests. In this paper, we describe the case of a 34-year-old male patient who presented compressive myelopathy secondary to spinal neurocysticercosis confirmed by polymerase chain reaction and histopathology report. The patient was successfully treated with decompressive surgery. We discuss the clinical aspects, the usefulness of diagnostic tools —including polymerase chain reaction—, and the therapeutic options available for the treatment of spinal neurocysticercosis.

AB - Neurocysticercosis is an endemic parasitic disease in several regions of the world. The spinal form is rare and its diagnosis is complex due to the clinical variability and the poor performance of the available additional tests. In this paper, we describe the case of a 34-year-old male patient who presented compressive myelopathy secondary to spinal neurocysticercosis confirmed by polymerase chain reaction and histopathology report. The patient was successfully treated with decompressive surgery. We discuss the clinical aspects, the usefulness of diagnostic tools —including polymerase chain reaction—, and the therapeutic options available for the treatment of spinal neurocysticercosis.

KW - Neurocysticercosis

KW - Polymerase chain reaction

KW - Spinal cord

UR - https://www.scopus.com/pages/publications/85048573056

U2 - 10.1016/j.neuarg.2018.03.002

DO - 10.1016/j.neuarg.2018.03.002

M3 - Artículo

AN - SCOPUS:85048573056

SN - 1853-0028

VL - 11

SP - 96

EP - 100

JO - Neurologia Argentina

JF - Neurologia Argentina

IS - 2

ER -

Compressive myelopathy secondary to spinal neurocysticercosis stablished by polymerase chain reaction

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