• Nenhum resultado encontrado

Arq. NeuroPsiquiatr. vol.72 número1

N/A
N/A
Protected

Academic year: 2018

Share "Arq. NeuroPsiquiatr. vol.72 número1"

Copied!
2
0
0

Texto

(1)

83

IMAGES IN NEUROLOGY

DOI:

10.1590/0004-282X20130206

Brainstem reversible leukoencephalopathy

syndrome

Síndrome da leucoencefalopatia reversível de tronco cerebral

Vera L. Braatz, Paulo José Lorenzoni, Cláudia S. K. Kay, Domingos C. Chula, Rosana H. Scola,

Lineu C. Werneck

A 39-year-old man presented with progressive

hea-dache, nauseas, blurriness and cortical blindness. Blood

pressure: 230x140 mmHg. Glasgow score: 15.

Fundos-copy revealed hypertensive retinopathy and papille

-

de ma. Neurological examination was normal. Brain ma

g-netic resonance imaging revealed area of swelling and high

signal on FLAIR-weighted images on the brainstem and

cerebral whitematter abnormalities (Figure 1). Hyperten

-sion management improved his clinical and radiological

indings (Figure 2).

Posterior reversible leukoencephalopathy syndrome (PRES),

with classical reversible cerebral vasogenic edema, occurred

predominantly in the posterior distribution (occipital and

pa-rietal lobes) on brain imaging

1-3

. he brainstem involvement

is an atypical feature which may be encountered in midbrain

(13%), pons (20%) and medulla oblongata (5%)

1-3

. his PRES

variant should be diferentiated from brainstem infarction,

pontine glioma, infective encephalitis, central pontine

mye-linolysis and others demyelinating disorders because PRES is

potentially full reversible after treatment

1-3

.

Divisão de Neurologia, Departamento de Clínica Médica,, Hospital de Clínicas, Universidade Federal do Paraná, Curitiba PR, Brazil.

Correspondence: Rosana Herminia Scola; Serviço de Doenças Neuromusculares; Hospital de Clínicas, Universidade Federal do Paraná; Rua General Carneiro 181 / 3o andar;

80060-900 Curitiba PR - Brasil; E-mail: scola@hc.ufpr.br Conflict of interest: There is no conflict of interest to declare.

Received 05 February 2013; Received in final form 11 July 2013; Accepted 18 July 2013.

Figure 1.

Initial brain magnetic resonance imaging revealed area of swelling and high signal on the brainstem (mainly in pons

and medulla oblongata) and cerebral white-matter abnormalities, which are compatible with the brainstem variant of posterior

reversible leukoencephalopathy syndrome (A, FLAIR-weighted images; B, diffusion-weighted images; C, T1-weighted images after

contrast infusion; D, apparent diffusion coefficient).

A

B

C

(2)

84

Arq Neuropsiquiatr 2014;72(1):83-84

1. Kitaguchi H, Tomimoto H, Miki Y, et al. A brainstem variant of reversible posterior leukoencephalopathy syndrome. Neuroradiology 2005;47:652-656.

2. Liman TG, Bohner G, Heuschmann PU, Endres M, Siebert E. The clinical and radiological spectrum of posterior reversible

References

encephalopathy syndrome: the retrospective Berlin PRES study. J Neurol 2012;259:155-164.

3. Stevens CJ, Heran MK. The many faces of posterior reversible encephalopathy syndrome. Br J Radiol 2012;85:1566-1575.

Figure 2.

After 6 months of the hypertension management, follow-up brain magnetic resonance imaging showed regression of

vasogenic edema that was graded as complete in brainstem (A, FLAIR-weighted images; B, diffusion-weighted images).

A

Imagem

Figure 1. Initial brain magnetic resonance imaging revealed area of swelling and high signal on the brainstem (mainly in pons  and medulla oblongata) and cerebral white-matter abnormalities, which are compatible with the brainstem variant of posterior  rev
Figure 2. After 6 months of the hypertension management, follow-up brain magnetic resonance imaging showed regression of  vasogenic edema that was graded as complete in brainstem (A, FLAIR-weighted images; B, diffusion-weighted images).

Referências

Documentos relacionados

OBJECTIVE: To determine the frequency and localization of parenchymal abnormalities in cerebral venous thrombosis on magnetic resonance imaging and magnetic resonance angiography

Magnetic resonance imaging (MRI) revealed a right-sided lesion, showing a hyperintense signal on T1-weighted images and a slightly hyperintense signal on T2-weighted images, lo-

A subsequent contrast- enhanced magnetic resonance imaging scan of the abdomen revealed a formation with intermediate signal intensity on T1- weighted images, heterogeneous

A subsequent contrast- enhanced magnetic resonance imaging scan of the abdomen revealed a formation with intermediate signal intensity on T1- weighted images, heterogeneous

This exam showed no abnormalities in the inner ears and multifocal white matter areas of slight low signal on T1-weighted images and high signal on FLAIR images (Fig 2).. The other

After this new neurological manifestation suggestive of MS, the patient was submitted to brain magnetic resonance imaging (MRI), which revealed multiple areas of high signal on

Cognitive and magnetic resonance imaging brain morphometric correlates of brain-derived neurotrophic factor Val66Met gene polymorphism in patients with schizophrenia and healthy

They found that 0.83% of patients presenting for psychiatric evaluation had white-matter hyperintensities on T2-weighted magnetic resonance imaging (MRI), and that these