4.3 Article

Long-term Prognosis of Localized Lymphoid Hyperplasia of the Rectum

Journal

GUT AND LIVER
Volume 15, Issue 1, Pages 77-84

Publisher

EDITORIAL OFFICE GUT & LIVER
DOI: 10.5009/gnl19288

Keywords

Lymphoid hyperplasia; Rectum; Colitis, ulcerative; Mucosa-associated lymphoid tissue lymphoma

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The majority of rectal LLH cases resolve spontaneously, but about 10% may develop into serious diseases such as UC or MALT lymphoma. Patients with nodular or submucosal tumor-like types may have a higher risk of developing clinically significant diseases. Risk stratification and careful surveillance are essential for these lesions.
Background/Aims: Although localized lymphoid hyperplasia (LLH) of the rectum is occasionally observed, its clinical implications are unclear. This study aimed to investigate the clinical course and significance of LLH of the rectum. Methods: We identified 65 patients diagnosed with LLH of the rectum using a histopathologic examination and who received follow-up endoscopies between January 2009 and June 2015. Patients with a history of inflammatory bowel disease, lymphoma, familial adenomatous polyposis, or uncontrolled malignancy and patients who underwent scar biopsy after endoscopic resection or surgery were excluded. Endoscopic findings and clinical courses were analyzed. Results: During the median follow-up of 31 months (interquartile range, 19 to 40 months), 81.5% (53/65) of LLHs of the rectum were resolved. Clinically significant diseases, including ulcerative colitis (UC, n=5) and mucosa-associated lymphoid tissue (MALT) lymphoma (n=1), were diagnosed in 9.2% of patients (6/65). The other six patients showed no significant changes in the lesion (n=3) or a waxing and waning appearance (n=3). According to endoscopic findings, all of the 47 polypoid types showed resolution or waxing and waning patterns. Five of the 11 nodular types (45.5%) developed into UC. One of the seven submucosal tumor (SMT)-like types (14.3%) developed into MALT lymphoma. Conclusions: LLH of the rectum with persistent symptoms or the endoscopic appearance of the nodular or SMT-like type may lead to clinically significant disease. Risk stratification according to endoscopic findings and careful surveillance are required for these lesions.

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