Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0014848 (
achalasia
)
2,804
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Inclusion body myositis
is an inflammatory myopathy in which dysphagia has been considered a rare finding. However, recent literature finds dysphagia an increasingly common symptom as more cases of
inclusion body myositis
are identified. Unlike some inflammatory myopathic disorders,
inclusion body myositis
is resistant to treatment with corticosteroids, and therefore, the otolaryngologist may be consulted regarding surgical options for relief of dysphagia. A patient is described in whom severe progressive dysphagia associated with
inclusion body myositis
developed. Impaired pharyngeal wall motion and cricopharyngeal
achalasia
were demonstrated by videofluoroscopic evaluation, and the patient was successfully treated by cricopharyngeal myotomy. The pathophysiologic nature of
inclusion body myositis
and the mechanisms of cervical dysphagia in the inflammatory myopathies are reviewed.
...
PMID:Management of dysphagia in inclusion body myositis. 131 47