A case of reactive lymphoid hyperplasia of the liver in a patient with autoimmune hepatitis

Author:

Kanno HirokiORCID,Sakai Hisamune,Hisaka Toru,Kojima Satoki,Midorikawa Ryuta,Fukutomi Shogo,Nomura Yoriko,Goto Yuichi,Sato Toshihiro,Yoshitomi Munehiro,Kawahara Ryuichi,Okuda Koji

Abstract

Abstract Background Reactive lymphoid hyperplasia (RLH) of the liver is a benign disorder. It is usually observed in the skin, orbit, thyroid, lung, breast, or gastrointestinal tract, but rarely in the liver. Since the first report of RLH of the liver in 1981, only 75 cases have been described in the past literature. Herein, we report a case of RLH of the liver in a patient with autoimmune hepatitis (AIH), which was misdiagnosed as hepatocellular carcinoma (HCC) preoperatively and resected laparoscopically. Case presentation A 43-year-old Japanese woman with autoimmune hepatitis was followed up for 5 years. During her medical checkup, a hypoechoic nodule in segment 6 of the liver was detected. The nodule had been gradually increasing in size for 4 years. Abdominal ultrasound (US) revealed a round, hypoechoic nodule, 12 mm in diameter. Contrast-enhanced computed tomography (CT) demonstrated that the nodule was slightly enhanced in the arterial dominant phase, followed by perinodular enhancement in the portal and late phases. A magnetic resonance imaging (MRI) scan showed low signal intensity on the T1-weighted image (T1WI) and slightly high signal intensity on the T2-weighted image (T2WI). The findings of the Gd-EOB-DTPA-enhanced MRI were similar to those of contrast-enhanced CT. Tumor markers were all within the normal range. The preoperative diagnosis was HCC and a laparoscopic right posterior sectionectomy was performed. Pathological examination revealed that the nodular lesion was infiltrated by small lymphocytes and plasma cells, and germinal centers were present. Immunohistochemistry was positive for B cell and T cell markers, indicating polyclonality. The final diagnosis was RLH of the liver. Conclusions The pathogenesis of RLH of the liver remains unknown, and a definitive diagnosis based on imaging findings is extremely difficult. If a small, solitary nodule is found in female patients with AIH, the possibility of RLH of the liver should be considered.

Publisher

Springer Science and Business Media LLC

Reference59 articles.

1. Snover DC, Filipovich AH, Dehner LP, Krivit W. ‘Pseudolymphoma’. A case associated with primary immunodeficiency disease and polyglandular failure syndrome. Arch Pathol Lab Med. 1981;105(1):46–9.

2. Grouls V. Pseudolymphoma (inflammatory pseudotumor) of the liver. Zentralbl Allg Pathol. 1987;133(6):565–8.

3. Isobe H, Sakamoto S, Sakai H, Masumoto A, Sonoda T, Adachi E, et al. Reactive lymphoid hyperplasia of the liver. J Clin Gastroenterol. 1993;16(3):240–4.

4. Ohtsu T, Sasaki Y, Tanizaki H, Kawano N, Ryu M, Satake M, et al. Development of pseudolymphoma of liver following interferon-alpha therapy for chronic hepatitis B. Intern Med. 1994;33(1):18–22.

5. Katayanagi K, Terada T, Nakanuma Y, Ueno T. A case of pseudolymphoma of the liver. Pathol Int. 1994;44(9):704–11.

Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3