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Erdheim-Chester disease: misdiagnosed as multiple sclerosis.
Yang, Jason; Imlay-Gillespie, Louise; Dierkes, Judith Gerarda; Khoo, Tien Kheng.
Afiliação
  • Yang J; Medicine, The University of Queensland - Saint Lucia Campus, Saint Lucia, Queensland, Australia drtwyang@gmail.com.
  • Imlay-Gillespie L; Haematology, Lismore Base Hospital, Lismore, New South Wales, Australia.
  • Dierkes JG; Rehabilitation, Ballina District Hospital, Ballina, New South Wales, Australia.
  • Khoo TK; School of Medicine and Dentistry, Griffith University, Gold Coast, Queensland, Australia.
Pract Neurol ; 24(2): 144-147, 2024 Mar 19.
Article em En | MEDLINE | ID: mdl-37932040
Erdheim-Chester disease is a rare histiocytic neoplasm with a wide range of clinical manifestations. Due to its rarity and protean characteristics, this condition often presents a diagnostic challenge. A Caucasian woman in her late 60s presented with unsteadiness, dysphagia and dysarthria. She was initially diagnosed with secondary progressive multiple sclerosis but deteriorated over 2 years with a potential lack of therapeutic response. Subsequent investigations resulted in the diagnosis of Erdheim-Chester disease. She received targeted therapy with BRAF and MAPK-pathway inhibitors. Her initial response to treatment has been positive with functional gains and reduced disease burden on MR brain imaging, and with no significant adverse effects.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Erdheim-Chester / Esclerose Múltipla Limite: Female / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Erdheim-Chester / Esclerose Múltipla Limite: Female / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article