A case report of leptomeningeal amyloidosis presenting with meningoencephalitis-resembling manifestations in a 54-year-old woman

We report a 54-year-old woman previously healthy who developed acute fever, headache, and impaired consciousness. We administered corticosteroid therapy as autoimmune mediated meningoencephalitis, which improved her symptoms and reduced cerebrospinal IL-6 level, but her cognitive impairment persisted. Contrast-enhanced MRI showed diffuse meningeal enhancement lesion, which led us to the possibility of leptomeningeal amyloidosis (LA). We performed transthyretin gene analysis identified heterozygosity for the c.265T>C, p.Y89H (Y69H) variant, which is known as one of the causative mutations of familial LA. Given the responsiveness to steroid treatment, it is possible that the inflammatory pathology related to amyloid deposition in leptomeninges with encephalitis-like symptoms contributed to the prolonged duration of symptoms lasting from hours to days.

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Rinsho Shinkeigaku
Published
2025-01-01
DOI
https://doi.org/10.5692/clinicalneurol.cn-002066
Primary Topic
Amyloidosis: Diagnosis, Treatment, Outcomes
Type
article
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article

A case report of leptomeningeal amyloidosis presenting with meningoencephalitis-resembling manifestations in a 54-year-old woman

Masaki Namekawa, Ryoma Kishi, Junsuke Shimbo, Kunihiko Makino et al.
Rinsho Shinkeigaku
Amyloidosis: Diagnosis, Treatment, Outcomes
article

A case report of leptomeningeal amyloidosis presenting with meningoencephalitis-resembling manifestations in a 54-year-old woman

Masaki Namekawa, Ryoma Kishi, Junsuke Shimbo, Kunihiko Makino, Kunihiko Wakaki, Naomi Suzuki, Takao Fukushima
article en

Abstract

We report a 54-year-old woman previously healthy who developed acute fever, headache, and impaired consciousness. We administered corticosteroid therapy as autoimmune mediated meningoencephalitis, which improved her symptoms and reduced cerebrospinal IL-6 level, but her cognitive impairment persisted. Contrast-enhanced MRI showed diffuse meningeal enhancement lesion, which led us to the possibility of leptomeningeal amyloidosis (LA). We performed transthyretin gene analysis identified heterozygosity for the c.265T>C, p.Y89H (Y69H) variant, which is known as one of the causative mutations of familial LA. Given the responsiveness to steroid treatment, it is possible that the inflammatory pathology related to amyloid deposition in leptomeninges with encephalitis-like symptoms contributed to the prolonged duration of symptoms lasting from hours to days.

Rinsho ShinkeigakuVol. 65(7)
Niigata Prefectural Shibata Hospital (JP)
Gender equality
Openalex Percentile: Top 87%
Amyloidosis: Diagnosis, Treatment, Outcomes
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A case report of leptomeningeal amyloidosis presenting with meningoencephalitis-resembling manifestations in a 54-year-old woman — Masaki Namekawa, Ryoma Kishi, et al. · Rinsho Shinkeigaku (2025) | TGRS Research Map | TGRS