Abstract

Acute hemorrhagic leukoencephalitis is a fulminant demyelinating disease and commonly considered as a rare and severe variant of acute disseminated encephalomyelitis. Here, we report the clinical, magnetic resonance imaging, and brain biopsy findings of a 35-year-old female with relapsing-remitting multiple sclerosis, who developed acute hemorrhagic leukoencephalitis. Magnetic resonance imaging revealed symmetrical hemorrhagic lesions in the basal ganglia including the thalami. Disease progression was consistent with acute hemorrhagic leukoencephalitis with rapid deterioration of consciousness and seizures. Besides hemorrhage, infiltration of neutrophils was detected in brain biopsy.Acute hemorrhagic leukoencephalitis, also known as Weston-Hurst syndrome, is an excessive immunological response of unknown etiology. So far, an association with multiple sclerosis has not been reported. The present case raises the question, whether acute hemorrhagic leukoencephalitis is a specific hyperacute form of acute disseminated encephalomyelitis, a severe and unspecific form of an immune response in the central nervous system, or belongs to the spectrum of tumefactive multiple sclerosis.

Highlights

  • Acute hemorrhagic leukoencephalitis (AHLE) was first described by Weston Hurst in 1941

  • AHLE is characterized by an acute onset and rapidly progressive inflammation with symmetrical, multifocal brain lesions associated with acute edematous necrosis and hemorrhage

  • The present case demonstrates an unusual presentation during a classical course of Multiple sclerosis (MS) leading to the diagnosis of AHLE

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Summary

Introduction

Acute hemorrhagic leukoencephalitis (AHLE) was first described by Weston Hurst in 1941. AHLE is characterized by an acute onset and rapidly progressive inflammation with symmetrical, multifocal brain lesions associated with acute edematous necrosis and hemorrhage. Internal venous thrombosis was ruled out by CT venous angiography; MRI revealed symmetrical hyperintense lesions in the basal ganglia on T1-weighted and punctate hemorrhages on T2-weighted images (Fig. 1c).

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Conclusion

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