Isolated AL Amyloidosis of the Colon: A Rare Presentation

Author:

Garcia Alexander1,Qureshi Mahir1ORCID,Dhawan Ishita2,Rafferty William3,Budak-Alpdogan Tulin4,Giordano Samuel2

Affiliation:

1. Department of Medicine, Cooper University Hospital, Camden, NJ

2. Department of Gastroenterology, Cooper University Hospital, Camden, NJ

3. Department of Pathology, Cooper University Hospital, Camden, NJ

4. Department of Hematology/Oncology, Cooper University Hospital, Camden, NJ

Abstract

ABSTRACT Amyloidosis is a group of rare deposition diseases marked by the accumulation of abnormal fibrillar proteins in the extracellular space of various tissues. In both AL and AA amyloidosis, the most common variants, isolated involvement to any one organ is uncommon and involvement to the colon alone is especially rare. We present the case of a patient who was initially found to have AL amyloidosis on prior screening colonoscopy that was reconfirmed several years with repeat evaluation for chronic constipation. This disease process is often insidious and can be overlooked by providers given the lack of overwhelming symptoms.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference15 articles.

1. Primary gastrointestinal amyloidosis: An unusual cause of acute intestinal pseudo-obstruction;Wetwittayakhlang;Case Rep Gastroenterol,2020

2. Primary localized amyloidosis of the intestine: A pathologist viewpoint;Alshehri;Gastroenterol Res,2020

3. A case of systemic AL amyloidosis diagnosed by screening colonoscopy;Alnimer;Case Rep Gastrointest Med,2022

4. Gastrointestinal amyloidosis: Review of the literature;Rowe;Cureus,2017

5. Primary localized amyloidosis of the intestine: A pathologist viewpoint;Alshehri;Gastroenterol Res,2020

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