Cited by 110Amyloidosis: Diagnosis, Treatment, OutcomesGastrointestinal motility and disordersPrion Diseases and Protein Misfolding

Gastrointestinal-motility dysfunction in amyloidosis

Battle, William M., Rubin, Marc R., Cohen, Sidney, Snape, William J.·1979·New England Journal of Medicine

Abstract

SYSTEMIC amyloidosis frequently involves the gastrointestinal tract and may result in obstruction, malabsorption, ulceration, hemorrhage or perforation as well as impaired motility.1 2 3 It is unclear whether the impaired gastrointestinal motility is secondary to the effects of amyloid on the smooth muscle or on the autonomic nervous system. We report on a patient with primary amyloidosis, in whom esophageal manometric and colonic myoelectric studies revealed a widespread disorder of gastrointestinal motility. The evidence suggests that neural dysfunction contributes to the abnormal motility associated with amyloidosis.Case ReportA 68-year-old woman was admitted to the Hospital of the University of Pennsylvania with . . .

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Crossref · 10.1056/nejm197907053010105

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  • Later stages of amyloidosis may show low-amplitude contractions reflecting myopathic infiltration of smooth muscle.

    “Manometric studies suggest that early disease can manifest with motor incoordination consistent with neural involvement, whereas later stages may show low-amplitude contractions reflecting myopathic infiltration of smooth muscle (Battle et al., 1979; Camilleri et al., 1985; Rubinow et al., 1983).”
  • Manometric studies suggest that early amyloidosis can manifest with motor incoordination consistent with neural involvement.

    “Manometric studies suggest that early disease can manifest with motor incoordination consistent with neural involvement, whereas later stages may show low-amplitude contractions reflecting myopathic infiltration of smooth muscle (Battle et al., 1979; Camilleri et al., 1985; Rubinow et al., 1983).”

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References 10 · Cited by 110

Authors
Battle, W. M., Rubin, M. R., Cohen, S., & Snape, W. J.
Affiliations
Hospital of the University of Pennsylvania (US)
Venue
New England Journal of Medicine
Published
1979-07-05
Volume
301
Issue
1
Pages
24-25
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2079783462
Cited by
110
References
10
Citations by year
2026: 1 · 2025: 1 · 2024: 1 · 2023: 2 · 2022: 1 · 2021: 3 · 2020: 2 · 2019: 2 · 2017: 1 · 2016: 3 · 2015: 1 · 2014: 2 · 2013: 1 · 2012: 3
FWCI
1.78
Type
journal article
Language
en
Open access
closed
Locations
  • New England Journal of Medicine (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Amyloidosis: Diagnosis, Treatment, Outcomes
  • Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Prion Diseases and Protein Misfolding
Keywords
systemic amyloidosis, AL amyloidosis, gastrointestinal motility disorders, esophageal manometry, autonomic dysfunction, smooth muscle dysfunction, esophageal motility disorders, colonic motility disorders
MeSH terms
Aged, Amyloidosis, Colon, Esophagogastric Junction, Esophagus, Female, Gastrointestinal Diseases, Gastrointestinal Motility, Humans, Manometry, Muscle, Smooth, Neostigmine, Nervous System Diseases, Neural Pathways, Peripheral Nervous System Diseases, Peristalsis, Pressure

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