TY - JOUR
T1 - Stiff Person Syndrome in a patient with atypical carcinoid tumor of the lung secondary to anti-amphiphysin antibodies
T2 - A case report and literature review
AU - Abusamra, Khawla
AU - Thandampallayam, Mangayarkarasi
AU - Lukins, Douglas
AU - Sudhakar, Padmaja
N1 - Publisher Copyright:
© 2022 The Author(s)
PY - 2022/1
Y1 - 2022/1
N2 - Background: Stiff Person Syndrome (SPS) is a rare neurological disorder of unclear etiology characterized by two set of symptoms; skeletal muscle stiffness and rigidity primarily affecting the truncal musculature due to continuous co-contracture of agonist and antagonist muscles, and superimposed episodic spasms axial rigidity, limb stiffness, difficulty walking, and postural instability. SPS is classified into classic SPS, paraneoplastic SPS, and SPS variants- that include segmental SPS, Jerky SPS, Progressive encephalomyelitis with rigidity and myoclonus, and SPS plus syndrome. Case report: we present the first reported case of SPS in association with atypical lung carcinoid in a 48-year-old male patient. He was diagnosed with SPS based on the progressive muscle stiffness and the amphiphysin antibody seropositivity in the setting of known atypical carcinoid Conclusion: This unusual case highlights the importance of keeping a high degree of suspicion for PSP when patients presents with typical symptoms in the sittings of known malignancy.
AB - Background: Stiff Person Syndrome (SPS) is a rare neurological disorder of unclear etiology characterized by two set of symptoms; skeletal muscle stiffness and rigidity primarily affecting the truncal musculature due to continuous co-contracture of agonist and antagonist muscles, and superimposed episodic spasms axial rigidity, limb stiffness, difficulty walking, and postural instability. SPS is classified into classic SPS, paraneoplastic SPS, and SPS variants- that include segmental SPS, Jerky SPS, Progressive encephalomyelitis with rigidity and myoclonus, and SPS plus syndrome. Case report: we present the first reported case of SPS in association with atypical lung carcinoid in a 48-year-old male patient. He was diagnosed with SPS based on the progressive muscle stiffness and the amphiphysin antibody seropositivity in the setting of known atypical carcinoid Conclusion: This unusual case highlights the importance of keeping a high degree of suspicion for PSP when patients presents with typical symptoms in the sittings of known malignancy.
UR - https://www.scopus.com/pages/publications/85149600103
UR - https://www.scopus.com/inward/citedby.url?scp=85149600103&partnerID=8YFLogxK
U2 - 10.1016/j.nerep.2022.100116
DO - 10.1016/j.nerep.2022.100116
M3 - Article
AN - SCOPUS:85149600103
VL - 2
JO - Neuroimmunology Reports
JF - Neuroimmunology Reports
M1 - 100116
ER -