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Refractory Rectal Lymphoid Follicular Hyperplasia Progressing to Lymphoid Follicular Proctitis, Report of a Case Sakae Mikami 1 , Yukimasa Yamashita 1 , Takayuki Nishigami 2 , Masayuki Maruo 1 , Eiki Son 1 , Ryosuke Itai 1 , Satoki Yasumura 1 , Eiji Ikeda 1 , Mariko Takada 1 , Yasuhiko Sumitomo 1 1Department of Gastroenterology and Hepatology, Kobe City Medical Center West Hospital, Kobe, Japan 2Department of Clinical Pathology, Steel Memorial Hirohata Hospital, Himeji, Japan Keyword: LFP , 直腸リンパ濾胞増殖症 , 潰瘍性大腸炎の初期病変 , 難治性 , 鑑別診断 pp.935-941
Published Date 2015/6/25
DOI https://doi.org/10.11477/mf.1403200349
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 A 26-year-old woman was referred to our hospital for treatment of rectal lymphoid follicular hyperplasia. She complained of intermittent mucus and blood in stools without diarrhea. Colonoscopy revealed a circumferential, uniform rectal mucosa of granular appearance without mucosal ulceration. Histological examination of rectal biopsy specimens demonstrated the presence of lymphoid follicles, hyperplasia, and infiltration of lymphocytes within the mucosal lamina propria. There was no evidence of crypt hyperplasia, atrophy, abscesses, granulomas, ulceration, neutrophilic infiltrates, or impaired mucus secretion. Lymphoid follicular proctitis was diagnosed. Initially, a conservative approach to management was taken because of the absence of symptom exacerbation. On developing mucoid stools and hematochezia, mesalazine and batamethasone suppository treatment were initiated without improvement in symptoms and endoscopic findings. The patient was followed-up for more than 5 years, and she did not develop ulcerative proctitis or other inflammatory disease. This case highlights the importance of ascertaining or ruling out potential diseases when diagnosing and managing lymphoid follicular proctitis.


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電子版ISSN 1882-1219 印刷版ISSN 0536-2180 医学書院

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