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Rheumatoid meningitis: a case series report and review of modern therapeutic schemes and outcome.
Serra Smith, Carlos; Montero Reyes, Fernando José; Contreras Chicote, Ana; Martínez Barrio, Julia; Vieru, Mihaela; Herrera Herrera, Isabel; Arias, Francisco; Martínez Ginés, Marisa; García Domínguez, Jose Manuel.
Afiliación
  • Serra Smith C; Neurology Department, Hospital General Universitario Gregorio Marañón, 46 Doctor Esquerdo Street, 28007, Madrid, Spain. caserra@ucm.es.
  • Montero Reyes FJ; Rheumatology Department, Hospital General Universitario Gregorio Marañón, 46 Doctor Esquerdo Street, 28007, Madrid, Spain.
  • Contreras Chicote A; Neurology Department, Hospital General Universitario Gregorio Marañón, 46 Doctor Esquerdo Street, 28007, Madrid, Spain.
  • Martínez Barrio J; Rheumatology Department, Hospital General Universitario Gregorio Marañón, 46 Doctor Esquerdo Street, 28007, Madrid, Spain.
  • Vieru M; Anatomical Pathology Department, Hospital General Universitario Gregorio Marañón, 46 Doctor Esquerdo Street, 28007, Madrid, Spain.
  • Herrera Herrera I; Neurorradiology Section, Radiology Department, Hospital General Universitario Gregorio Marañón, 46 Doctor Esquerdo Street, 28007, Madrid, Spain.
  • Arias F; Anatomical Pathology Department, Hospital General Universitario Gregorio Marañón, 46 Doctor Esquerdo Street, 28007, Madrid, Spain.
  • Martínez Ginés M; Neurology Department, Hospital General Universitario Gregorio Marañón, 46 Doctor Esquerdo Street, 28007, Madrid, Spain.
  • García Domínguez JM; Neurology Department, Hospital General Universitario Gregorio Marañón, 46 Doctor Esquerdo Street, 28007, Madrid, Spain.
Neurol Sci ; 2024 Jul 16.
Article en En | MEDLINE | ID: mdl-39009895
ABSTRACT

INTRODUCTION:

Rheumatoid meningitis (RM) is an extremely rare extra-articular complication of rheumatoid arthritis (RA), with approximately 165 cases reported world-wide. RM exhibits a broad range of symptoms, with stroke-like episodes and seizures being the most common manifestations. The primary differential diagnoses include vascular and infectious diseases. The influence of immunomodulatory medications on the pathophysiology of RM remains unclear. There are no consensus guidelines on therapeutic regimen.

METHODS:

We present four patients with prior history of RA that developed different neurological syndromes in correlation to radiological leptomeningitis. Clinical presentations, comorbid conditions, supplementary diagnostic assessments, treatments, and prognosis are provided. A literature review of recent immunosuppressive management in RM patients was performed.

RESULTS:

Three patients presented to hospital with recurrent focal seizures. Only two suffered meningism, reporting headache and fever. Magnetic resonance imaging (MRI) showed different grades of leptomeningitis across all cases. Notably, three cases demonstrated bilateral involvement extending to the pachymeninges. Two patients exhibited pronounced CSF mononuclear inflammation while extended microbiological evaluations yielded negative results. Two patients required biopsy for confirmation. The initiation of immunosuppressive therapy marked a turning point for three patients who previously exhibited progressive deterioration. Mortality was absent in all cases.

CONCLUSIONS:

Our experience remarks the elusive nature of RM. Rigorous exclusionary diagnostics are imperative to differentiate RM from mimicking conditions. Clinical manifestations oscillate between transient episodes and progressive neurological impairments, punctuated by frequent epileptic seizures. In scenarios where clinical worsening persists or where clinical and radiological evaluations are inconclusive, aggressive immunosuppressive therapy is recommended.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Neurol Sci Asunto de la revista: NEUROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Neurol Sci Asunto de la revista: NEUROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: España