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A case report of autoimmune necrotizing myositis presenting as dysphagia and neck swelling.
Ngo, Linh Q; Wu, Andrew G; Nguyen, Matthew A; McPherson, Lauren E; Gertner, Elie.
Afiliação
  • Ngo LQ; Division of Rheumatology, University of Minnesota Medical School, MMC 108 Mayo, 8108A, 420 Delaware St SE, Minneapolis, MN 55455 USA.
  • Wu AG; Department of Internal Medicine, University of Minnesota Medical School, Minneapolis, MN USA.
  • Nguyen MA; Department of Internal Medicine, University of Minnesota Medical School, Minneapolis, MN USA.
  • McPherson LE; Department of Internal Medicine, University of Minnesota Medical School, Minneapolis, MN USA.
  • Gertner E; Division of Rheumatology, University of Minnesota Medical School, MMC 108 Mayo, 8108A, 420 Delaware St SE, Minneapolis, MN 55455 USA ; Section of Rheumatology, Regions Hospital, Saint Paul, MN USA.
Article em En | MEDLINE | ID: mdl-27190496
ABSTRACT

BACKGROUND:

Severe dysphagia may occur in the immune mediated necrotizing myopathies (IMNM). Neck swelling and severe dysphagia as the initial symptoms upon presentation has not been previously described. CASE PRESENTATION A 55-year-old male with a 4 week history of neck swelling, fatigue, dysphagia, myalgias, night sweats, and cough was admitted for an elevated CK. He underwent extensive infectious and inflammatory evaluation including neck imaging and muscle biopsy. Neck CT and MRI showed inflammation throughout his strap muscles, retropharyngeal soft tissues and deltoids. Infectious work up was negative. Deltoid muscle biopsy demonstrated evidence of IMNM. Lab tests revealed anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) antibodies confirming the diagnosis of HMGCR IMNM.

CONCLUSIONS:

HMGCR IMNM is a rare and incompletely understood disease process. Awareness of HMGCR IMNM could potentially lead to earlier diagnosis, treatment and improved clinical outcomes as disease progression can be rapid and severe.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article