Small-Bowel Obstruction due to AA Amyloidosis in Presumed Extrapulmonary Tuberculosis
- 1Department of Gastroenterology, Northern Health, Melbourne, Victoria, Australia
- 2Department of Infectious Disease, Northern Health, Melbourne, Victoria, Australia
- 3Department of Anatomical Pathology, Northern Health, Melbourne, Victoria, Australia
Abstract
AA amyloidosis is rare in resource-rich settings, but remains prevalent in regions with untreated infection, particularly tuberculosis. We describe a case in Australia of a 68-year-old Somali-born woman with recurrent small-bowel obstruction, weight loss, and retroperitoneal lymphadenopathy. While colonoscopy was macroscopically normal, small-bowel biopsies revealed Congo red-positive AA amyloidosis. Lymph-node biopsy showed histiocytes with granulomatous inflammation, and tuberculosis testing was negative. Given epidemiologic factors and chronic inflammation, culture-negative tuberculosis with AA amyloidosis sequelae was presumed. Empirical tuberculous treatment led to clinical improvement and resolution of PET-avid lymphadenopathy, highlighting an unusual case of infiltrative small-bowel disease.
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BibTeX
@article{wees2026smallbowel,
title = {{Small-Bowel Obstruction due to AA Amyloidosis in Presumed Extrapulmonary Tuberculosis}},
author = {Jacoba van Wees and Terry Yan and Robin Sia and Diana Moir and Irene Lu and Diana Lewis},
journal = {ACG case reports journal},
year = {2026},
month = oct,
doi = {10.14309/crj.0000000000002392},
url = {https://europepmc.org/article/PMC/PMC13722498},
note = {CC BY-NC-ND},
}
RIS
TY - JOUR
TI - Small-Bowel Obstruction due to AA Amyloidosis in Presumed Extrapulmonary Tuberculosis
AU - Jacoba van Wees
AU - Terry Yan
AU - Robin Sia
AU - Diana Moir
AU - Irene Lu
AU - Diana Lewis
PY - 2026
DA - 2026/10/30
JO - ACG case reports journal
DO - 10.14309/crj.0000000000002392
UR - https://europepmc.org/article/PMC/PMC13722498
AB - AA amyloidosis is rare in resource-rich settings, but remains prevalent in regions with untreated infection, particularly tuberculosis. We describe a case in Australia of a 68-year-old Somali-born woman with recurrent small-bowel obstruction, weight loss, and retroperitoneal lymphadenopathy. While colonoscopy was macroscopically normal, small-bowel biopsies revealed Congo red-positive AA amyloidosis. Lymph-node biopsy showed histiocytes with granulomatous inflammation, and tuberculosis testing was negative. Given epidemiologic factors and chronic inflammation, culture-negative tuberculosis with AA amyloidosis sequelae was presumed. Empirical tuberculous treatment led to clinical improvement and resolution of PET-avid lymphadenopathy, highlighting an unusual case of infiltrative small-bowel disease.
SN - 2326-3253
ER -