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The “hot cross bun sign” in patients with autoimmune cerebellar ataxia: A case report and literature review

OBJECTIVES: The “hot cross bun sign” (HCBs) on magnetic resonance imaging (MRI) has been initially considered specific for multiple system atrophy with cerebellar features. However, a number of other conditions have since been described, which may be associated with this imaging sign. We herein desc...

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Autores principales: Liu, Mange, Ren, Haitao, Lin, Nan, Tan, Ying, Fan, Siyuan, Guan, Hongzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437433/
https://www.ncbi.nlm.nih.gov/pubmed/36062012
http://dx.doi.org/10.3389/fneur.2022.979203
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author Liu, Mange
Ren, Haitao
Lin, Nan
Tan, Ying
Fan, Siyuan
Guan, Hongzhi
author_facet Liu, Mange
Ren, Haitao
Lin, Nan
Tan, Ying
Fan, Siyuan
Guan, Hongzhi
author_sort Liu, Mange
collection PubMed
description OBJECTIVES: The “hot cross bun sign” (HCBs) on magnetic resonance imaging (MRI) has been initially considered specific for multiple system atrophy with cerebellar features. However, a number of other conditions have since been described, which may be associated with this imaging sign. We herein describe a patient with anti-Ri and paraneoplastic cerebellar ataxia, and review the association of the HCBs on imaging with various neurological autoimmune conditions. METHODS: We report a 40-year-old woman with anti-Ri-associated paraneoplastic neurological syndrome and breast carcinoma, in whom brain MRI revealed the HCBs late in the disease course. We also reviewed similar cases reported in the literature. RESULTS: The patient presented with cerebellar ataxia, polyneuropathy, and pyramidal signs. Although brain MRI was initially unremarkable, the HCBs and T2-weighted hyperintensity of the bilateral middle cerebellar peduncles were observed at later follow-up. Anti-Ri was detected in the serum and cerebrospinal fluid. Breast adenocarcinoma was confirmed via an axillary lymph node biopsy. Her symptoms partially resolved after the first corticosteroid pulse. However, subsequent immunotherapy and tumor treatments were ineffective. Four autoimmune cerebellar ataxia cases with the HCBs (two paraneoplastic and two non-paraneoplastic) were identified in the literature. DISCUSSION: The HCBs can be associated with paraneoplastic and non-paraneoplastic cerebellar ataxia, which may reflect neurodegeneration secondary to autoimmune injury. Thus, the HCBs should not be considered a contraindication for autoimmune cerebellar syndrome.
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spelling pubmed-94374332022-09-03 The “hot cross bun sign” in patients with autoimmune cerebellar ataxia: A case report and literature review Liu, Mange Ren, Haitao Lin, Nan Tan, Ying Fan, Siyuan Guan, Hongzhi Front Neurol Neurology OBJECTIVES: The “hot cross bun sign” (HCBs) on magnetic resonance imaging (MRI) has been initially considered specific for multiple system atrophy with cerebellar features. However, a number of other conditions have since been described, which may be associated with this imaging sign. We herein describe a patient with anti-Ri and paraneoplastic cerebellar ataxia, and review the association of the HCBs on imaging with various neurological autoimmune conditions. METHODS: We report a 40-year-old woman with anti-Ri-associated paraneoplastic neurological syndrome and breast carcinoma, in whom brain MRI revealed the HCBs late in the disease course. We also reviewed similar cases reported in the literature. RESULTS: The patient presented with cerebellar ataxia, polyneuropathy, and pyramidal signs. Although brain MRI was initially unremarkable, the HCBs and T2-weighted hyperintensity of the bilateral middle cerebellar peduncles were observed at later follow-up. Anti-Ri was detected in the serum and cerebrospinal fluid. Breast adenocarcinoma was confirmed via an axillary lymph node biopsy. Her symptoms partially resolved after the first corticosteroid pulse. However, subsequent immunotherapy and tumor treatments were ineffective. Four autoimmune cerebellar ataxia cases with the HCBs (two paraneoplastic and two non-paraneoplastic) were identified in the literature. DISCUSSION: The HCBs can be associated with paraneoplastic and non-paraneoplastic cerebellar ataxia, which may reflect neurodegeneration secondary to autoimmune injury. Thus, the HCBs should not be considered a contraindication for autoimmune cerebellar syndrome. Frontiers Media S.A. 2022-08-19 /pmc/articles/PMC9437433/ /pubmed/36062012 http://dx.doi.org/10.3389/fneur.2022.979203 Text en Copyright © 2022 Liu, Ren, Lin, Tan, Fan and Guan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Liu, Mange
Ren, Haitao
Lin, Nan
Tan, Ying
Fan, Siyuan
Guan, Hongzhi
The “hot cross bun sign” in patients with autoimmune cerebellar ataxia: A case report and literature review
title The “hot cross bun sign” in patients with autoimmune cerebellar ataxia: A case report and literature review
title_full The “hot cross bun sign” in patients with autoimmune cerebellar ataxia: A case report and literature review
title_fullStr The “hot cross bun sign” in patients with autoimmune cerebellar ataxia: A case report and literature review
title_full_unstemmed The “hot cross bun sign” in patients with autoimmune cerebellar ataxia: A case report and literature review
title_short The “hot cross bun sign” in patients with autoimmune cerebellar ataxia: A case report and literature review
title_sort “hot cross bun sign” in patients with autoimmune cerebellar ataxia: a case report and literature review
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437433/
https://www.ncbi.nlm.nih.gov/pubmed/36062012
http://dx.doi.org/10.3389/fneur.2022.979203
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