Neuromyelitis optica: a challenging diagnosis at secondary hospital

Known since the 19th century, neuromyelitis optica (NMO), or Devic’s disease, is an idiopathic immune-mediated inflammatory demyelinating disease of the central nervous system selectively affecting the optic nerve and spinal cord. Commonly diagnosed in demyelinating diseases reference centers, we re...

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Main Authors: Anna Paula Romero de Oliveira, Patrícia Taranto, Lívia Herbst, André Kirihara, Maira Leticia Veras, André Macedo Serafim Silva, Marcio Ricardo Taveira Garcia, Angelina Maria Martins Lino
Format: Article
Language:English
Published: University of São Paulo 2013-03-01
Series:Autopsy and Case Reports
Subjects:
Online Access:http://www.revistas.usp.br/autopsy/article/view/58877
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spelling doaj-e4bca04503cb478cb74ff36996ba05262020-11-24T21:07:57ZengUniversity of São PauloAutopsy and Case Reports2236-19602013-03-013110.4322/acr.%y.5887757825Neuromyelitis optica: a challenging diagnosis at secondary hospitalAnna Paula Romero de Oliveira0Patrícia Taranto1Lívia Herbst2André Kirihara3Maira Leticia Veras4André Macedo Serafim Silva5Marcio Ricardo Taveira Garcia6Angelina Maria Martins Lino7Scientific Division – Instituto de Infectologia Emílio Ribas, São Paulo/SP – BrazilDepartment of Internal Medicine – Hospital Universitário – Universidade de São Paulo, São Paulo/SP – BrazilDepartment of Internal Medicine – Hospital Universitário – Universidade de São Paulo, São Paulo/SP – BrazilDepartment of Internal Medicine – Hospital Universitário – Universidade de São Paulo, São Paulo/SP – BrazilDepartment of Internal Medicine – Hospital Universitário – Universidade de São Paulo, São Paulo/SP – BrazilDepartment of Internal Medicine – Hospital Universitário – Universidade de São Paulo, São Paulo/SP – BrazilDepartment of Radiology - Hospital das Clínicas - Faculdade de Medicina - Universidade de São Paulo, São Paulo/SP – BrazilDepartment of Internal Medicine – Hospital Universitário – Universidade de São Paulo, São Paulo/SP – BrazilKnown since the 19th century, neuromyelitis optica (NMO), or Devic’s disease, is an idiopathic immune-mediated inflammatory demyelinating disease of the central nervous system selectively affecting the optic nerve and spinal cord. Commonly diagnosed in demyelinating diseases reference centers, we report an 18-year-old female patient who sought medical attention with a 3-month history of weight loss, headache, and vomiting, followed by diplopia, a burning sensation over the lower limbs, and difficulty walking. A few days prior to hospital admission, the muscle strength in her lower limbs became worse and ascended to the upper limbs associated with sensory changes in the trunk and voiding dysfunction. At admission, the neurological examination was consistent with a spinal cord syndrome. After few days of hospitalization, she was tetraplegic with severe signs of brainstem involvement requiring mechanical ventilatory support. Intravenous methylprednisolone and cyclophosphamide were promptly started after ruling out the diagnosis of infectious disease and cord compression. Due to no substantial early improvement, intravenous immunoglobulin was also used. From then on, the neurological status gradually improved. Magnetic resonance imaging showed extensive demyelinating features in the spinal cord, and the serum IgG autoantibody was negative. The patient was referred to a tertiary neurological reference center where she remains under treatment.http://www.revistas.usp.br/autopsy/article/view/58877Neuromyelitis OpticaDemyelinating DiseasesRespiratory InsufficiencyMagnetic Resonance ImagingPulse TherapyDrug
collection DOAJ
language English
format Article
sources DOAJ
author Anna Paula Romero de Oliveira
Patrícia Taranto
Lívia Herbst
André Kirihara
Maira Leticia Veras
André Macedo Serafim Silva
Marcio Ricardo Taveira Garcia
Angelina Maria Martins Lino
spellingShingle Anna Paula Romero de Oliveira
Patrícia Taranto
Lívia Herbst
André Kirihara
Maira Leticia Veras
André Macedo Serafim Silva
Marcio Ricardo Taveira Garcia
Angelina Maria Martins Lino
Neuromyelitis optica: a challenging diagnosis at secondary hospital
Autopsy and Case Reports
Neuromyelitis Optica
Demyelinating Diseases
Respiratory Insufficiency
Magnetic Resonance Imaging
Pulse Therapy
Drug
author_facet Anna Paula Romero de Oliveira
Patrícia Taranto
Lívia Herbst
André Kirihara
Maira Leticia Veras
André Macedo Serafim Silva
Marcio Ricardo Taveira Garcia
Angelina Maria Martins Lino
author_sort Anna Paula Romero de Oliveira
title Neuromyelitis optica: a challenging diagnosis at secondary hospital
title_short Neuromyelitis optica: a challenging diagnosis at secondary hospital
title_full Neuromyelitis optica: a challenging diagnosis at secondary hospital
title_fullStr Neuromyelitis optica: a challenging diagnosis at secondary hospital
title_full_unstemmed Neuromyelitis optica: a challenging diagnosis at secondary hospital
title_sort neuromyelitis optica: a challenging diagnosis at secondary hospital
publisher University of São Paulo
series Autopsy and Case Reports
issn 2236-1960
publishDate 2013-03-01
description Known since the 19th century, neuromyelitis optica (NMO), or Devic’s disease, is an idiopathic immune-mediated inflammatory demyelinating disease of the central nervous system selectively affecting the optic nerve and spinal cord. Commonly diagnosed in demyelinating diseases reference centers, we report an 18-year-old female patient who sought medical attention with a 3-month history of weight loss, headache, and vomiting, followed by diplopia, a burning sensation over the lower limbs, and difficulty walking. A few days prior to hospital admission, the muscle strength in her lower limbs became worse and ascended to the upper limbs associated with sensory changes in the trunk and voiding dysfunction. At admission, the neurological examination was consistent with a spinal cord syndrome. After few days of hospitalization, she was tetraplegic with severe signs of brainstem involvement requiring mechanical ventilatory support. Intravenous methylprednisolone and cyclophosphamide were promptly started after ruling out the diagnosis of infectious disease and cord compression. Due to no substantial early improvement, intravenous immunoglobulin was also used. From then on, the neurological status gradually improved. Magnetic resonance imaging showed extensive demyelinating features in the spinal cord, and the serum IgG autoantibody was negative. The patient was referred to a tertiary neurological reference center where she remains under treatment.
topic Neuromyelitis Optica
Demyelinating Diseases
Respiratory Insufficiency
Magnetic Resonance Imaging
Pulse Therapy
Drug
url http://www.revistas.usp.br/autopsy/article/view/58877
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