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ArticleBMC neurology2024

Case report: orthostatic hypotension as the first presentation of progressive encephalomyelitis with rigidity and myoclonus (PERM) with multiple autoimmune antibodies.

Jinyi Song, Shanshan Hu, Liang Chen, Chaoyang Lan, Peilin Lu

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In one paragraph

Article in BMC neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jinyi SongSchool of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Shanshan HuDepartment of Neurology, Longyou People's Hospital, Quzhou, Zhejiang, China.
Liang ChenDepartment of Neurology, Tonglu County Second People's Hospital, Tonglu, Zhejiang, China.
Chaoyang LanDepartment of Neurology, Longyou People's Hospital, Quzhou, Zhejiang, China.
Peilin LuDepartment of Neurology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China. zxa2004@zju.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionStiff person syndrome (SPS) is a rare disease characterized by axial and lower-extremity muscle rigidity, muscle spasm, and pain. Progressive encephalomyelitis with rigidity and myoclonus (PERM) is a variant of SPS. This case is particularly notable for its uncommon initial symptom: orthostatic hypotension, coupled with the presence of multiple antibodies. Such a presentation is a rarity in the context of PERM, thus providing a fresh and unique angle for both diagnosis and treatment. CASE PRESENTATION: This case presents a 71-year-old man who was ultimately diagnosed with progressive encephalomyelitis with rigidity and myoclonus (PERM). His initial symptom was orthostatic hypotension, and we detected multiple antibodies such as GlyR antibody, GAD antibody, GM1-IgG and GQ1b-IgG in his serum. The patient showed partial response to glucocorticoid and immunoglobulin therapies, but as the disease recurred and progressed, plasma exchange, rituximab, and cyclophosphamide immunosuppressive therapy was administered, the prognosis remained poor. During follow-up after treatment, the patient developed pulmonary embolism and cardiac arrest, and died.

conclusionPERM exhibits diverse manifestation and pathogenic mechanisms. Immune heterogeneity affects clinical symptoms and prognosis. Cases of PERM combined with orthostatic hypotension and various antibodies have rarely been reported, the incidence and the specific mechanism is unknown, underscoring the need for further research. This case report underscores the importance of recognizing the diverse clinical presentations of PERM and the challenges in its diagnosis and management. It highlights autonomic dysfunction may be as the initial symptom of PERM. Moreover, it emphasizes the limitations of current treatment modalities and the necessity for further research to elucidate the underlying mechanisms and optimize therapeutic approaches for this debilitating autoimmune condition.

Indexed as

AutoantibodiesEncephalomyelitisHypotension, OrthostaticMuscle RigidityMyoclonusAgedHumansMaleAutoantibodiesAnti-glutamic acid decarboxylase antibodyAnti-glycine antibodyAnti-GM1 antibodyAnti-GQ1b antibodyCase reportProgressive encephalomyelitis with rigidity and myoclonus

Identifiers

PMID39522020
PMCPMC11549869

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