Please use this identifier to cite or link to this item: 10.2174/1874205X-v16-e2112241
Title: Involvement of the Nervous System in Systemic Sclerosis
Authors: Polunosika, Elīna
Pastare, Daina
Jaunozoliņa, Līga
Karelis, Guntis
Department of Neurology and Neurosurgery
Department of Infectology
Keywords: Scleroderma;Demyelinating;Nervous system;Immunomodulatory;Medications;Peripheral nervous system;3.2 Clinical medicine;1.1. Scientific article indexed in Web of Science and/or Scopus database
Issue Date: Feb-2022
Citation: Polunosika , E , Pastare , D , Jaunozoliņa , L & Karelis , G 2022 , ' Involvement of the Nervous System in Systemic Sclerosis ' , Open Neurology Journal , vol. 16 , e1874205X2112241 . https://doi.org/10.2174/1874205X-v16-e2112241
Abstract: Introduction: Scleroderma is a rare heterogeneous multisystem autoimmune disease. The disease is characterized by structural abnormalities of the small blood vessels. Scleroderma affects all organs of the body. Skin manifestations are commonly reported, but peripheral nervous system (PNS) and central nervous system (CNS) involvement has been less frequently reported. Neurological manifestations are broad, and it is challenging for clinicians to confirm a diagnosis of scleroderma. Case Presentation: In our case, a 53-year-old white woman had extensive clinical presentations: skin rashes and symptoms from internal organs, CNS, and PNS during the previous 11 years. She had not undergone any specific treatment because diagnosis has not been made in the early stages. Conclusion: It is important to make the diagnosis as early as possible and start treatment with immunomodulatory and immunosuppressant medication, as it affects the patient's disease progression, quality of life, and mortality. A detailed medical history, physical examination, and laboratory and radiology findings help us to identify and diagnose scleroderma. But unfortunately, it was late, and the patient died. This case guides us to be more careful and make the diagnosis of scleroderma earlier in the future.
Description: Publisher Copyright: © 2022 Polunosika et al.
DOI: 10.2174/1874205X-v16-e2112241
ISSN: 1874-205X
Appears in Collections:Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure

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