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Chronic inflammatory demyelinating polyradiculoneuropathy associated with Sjögren`s syndrome in a child.
Süt, Nursah Yeniay; Kartal, Ayse Tugba; Ertem, Seyma; Aydin, Fatma; Yildirim, Miraç; Bektas, Ömer; Özçakar, Zeynep Birsin; Teber, Serap.
Afiliación
  • Süt NY; Department of Pediatric Neurology, Ankara University Faculty of Medicine, Ankara.
  • Kartal AT; Department of Pediatric Neurology, Ankara University Faculty of Medicine, Ankara.
  • Ertem S; Department of Pediatric Rheumatology, Ankara University Faculty of Medicine, Ankara, Türkiye.
  • Aydin F; Department of Pediatric Rheumatology, Ankara University Faculty of Medicine, Ankara, Türkiye.
  • Yildirim M; Department of Pediatric Neurology, Ankara University Faculty of Medicine, Ankara.
  • Bektas Ö; Department of Pediatric Neurology, Ankara University Faculty of Medicine, Ankara.
  • Özçakar ZB; Department of Pediatric Rheumatology, Ankara University Faculty of Medicine, Ankara, Türkiye.
  • Teber S; Department of Pediatric Neurology, Ankara University Faculty of Medicine, Ankara.
Turk J Pediatr ; 65(1): 155-160, 2023.
Article en En | MEDLINE | ID: mdl-36866997
BACKGROUND: Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a peripheral nervous system disease associated with polyautoimmunity. CASE: We report a previously healthy 13-year old boy who was referred to our outpatient clinic with gait disturbance and distal lower limb weakness that had been increasing for six months. The patient had decreased deep tendon reflexes in the upper extremities and absence in the lower extremities, reduced muscle strength in the distal and proximal lower extremities, muscle atrophy, drop foot, and normal pinprick sensations. The patient was diagnosed with CIDP as a result of clinical findings and electrophysiological studies. Autoimmune diseases and infectious agents were investigated in terms of triggering CIDP. Although there was no clinical sign other than polyneuropathy, he was also diagnosed with Sjögren`s syndrome due to positive antinuclear antibodies and antibodies against Ro52, and with autoimmune sialadenitis. After six months of monthly intravenous immunoglobulin and oral methylprednisolone treatments, the patient was able to dorsiflex his left foot and walk without support. CONCLUSIONS: To our knowledge, our case is the first pediatric case with the coexistence of Sjögren`s syndrome and CIDP. Therefore, we suggest investigating children with CIDP in terms of underlying autoimmune diseases such as Sjögren`s syndrome.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Autoinmunes / Polirradiculoneuropatía Crónica Inflamatoria Desmielinizante Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Adolescent / Humans / Male Idioma: En Revista: Turk J Pediatr Año: 2023 Tipo del documento: Article Pais de publicación: Turquía

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Autoinmunes / Polirradiculoneuropatía Crónica Inflamatoria Desmielinizante Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Adolescent / Humans / Male Idioma: En Revista: Turk J Pediatr Año: 2023 Tipo del documento: Article Pais de publicación: Turquía