Protein-losing Enteropathy Complicated with Primary Intestinal Follicular Lymphoma

3Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

Abstract

Protein-losing enteropathy (PLE) is a rare syndrome characterized by hypoproteinemia due to gastrointestinal (GI) protein loss. Primary intestinal follicular lymphoma (PIFL), a specific variant of follicular lymphoma with essential only GI involvement, has not been reported as an etiology of PLE. We herein report a case of PLE complicated with PIFL that was successfully treated with rituximab, resulting in rapid improvement of PLE and a complete response of PIFL. Macroscopic findings of ulcerative lesions with diffuse involvement, which were precisely described by capsule and double-balloon enteroscopy at the diagnosis, also improved following the treatment. This case provides a clue suggesting factors that promote PLE in PIFL.

Cite

CITATION STYLE

APA

Minemura, T., Kikuchi, S., Mihara, H., Kamihara, Y., Wada, A., Fuchino, M., … Sato, T. (2022). Protein-losing Enteropathy Complicated with Primary Intestinal Follicular Lymphoma. Internal Medicine. Japanese Society of Internal Medicine. https://doi.org/10.2169/internalmedicine.8261-21

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free