肝淋巴组织不典型增生合并干燥综合征1例报告

杨潇; 周晓; 母小新; 吴金道; 胡春阳; 孔连宝

doi:10.3969/j.issn.1001-5256.2020.06.033

肝淋巴组织不典型增生合并干燥综合征1例报告

DOI: 10.3969/j.issn.1001-5256.2020.06.033

1. 南京医科大学第一临床医学院
2. 南京医科大学第一附属医院肝胆中心
3. 中国医学科学院肝脏移植重点实验室

基金项目:

国家自然科学基金(81871260)；

详细信息

中图分类号: R575;R593.2
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出版历程
- 出版日期: 2020-06-20

A case of atypical hepatic lymphoid hyperplasia with Sjogren’s syndrome

Research funding:

摘要

摘要:
<正>肝淋巴组织不典型增生（atypical lymphoid hyperplasia,ALH）是一类发生于肝脏的无法确定良恶性质的淋巴组织异常增生性病变,其病理学表现既不同于反应性淋巴组织增生,疑似却又无法确诊为淋巴瘤[1]。ALH主要包括部分难以确诊的早期淋巴瘤及各种不明原因引发的特殊增生性病变[2]。本例肝ALH有发展成为黏膜相关淋巴组织（mucosal associated lymphoid tissue,MALT）淋巴瘤的趋势,属于肝MALT淋巴瘤
- 淋巴组织增殖性疾病 /
- 淋巴瘤,非霍奇金 /
- 干燥综合征
- lymphoproliferative disorders /
- lymphoma,non-hodgkin /
- sjogren's syndrome

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参考文献(14)

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