Successful treatment of stiff-person syndrome with plasmapheresis: case report and literature review
Case Reports
M. Nasvytis
Vilnius University, Lithuania
R. Kaladytė Lokominienė
Vilnius University, Lithuania
Published 2023-10-03
https://doi.org/10.29014/NS.2022.26.22
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Keywords

stiff-person syndrome
antibodies against glutamic acid decarboxylase
plasmapheresis

How to Cite

1.
Nasvytis M, Kaladytė Lokominienė R. Successful treatment of stiff-person syndrome with plasmapheresis: case report and literature review. NS [Internet]. 2023 Oct. 3 [cited 2024 Jul. 18];26(3 (93):155-60. Available from: https://www.journals.vu.lt/neurologijos_seminarai/article/view/33274

Abstract

Stiff-person syndrome (SPS) is a rare neurologic disease, most often caused by autoimmune process during which antibodies against glutamic acid decarboxylase (anti-GAD65) are synthesised. The main clinical symptoms, among which are axial and proximal leg muscle stiffness and painful spasms, are often provoked by external triggers. In addition to those, the disease presents with anxiety, phobias, and other psychiatric symptoms. The most notable SPS comorbidities include temporal lobe epilepsy and type 1 diabetes mellitus. In this article, we present a clinical case of a patient illustrating the course of the disease, diagnostic difficulties, and treatment options, all of which are discussed in the literature review.

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