摘要
假性淋巴瘤又称反应性淋巴组织增生或结节性淋巴组织样增生,可发生于胃肠道,胰腺,眼眶,皮肤等.而肝脏的假性淋巴瘤极少发生,目前文献多为个案报道,对其发病机制、诊断及治疗预后等多方面缺乏系统性认识.肝假性淋巴瘤的临床表现缺乏特异性,影像学检查及肿瘤标志物常无明显特征.该病确诊主要依赖术后病理与免疫组化染色及基因学检查,及时完整的手术切除是目前首选的治疗方法.
Pseudolymphoma,also known as reactive lymphoid hyperplasia or nodular lymphoid lesion,can occur in the gastrointestinal tract,pancreas,eyelids,skin,etc.;however,pseudolymphoma of the liver rarely occurs.Because of the small number of individual case reports of hepatic pseudolymphoma in most institutions,there is a lack of information available regarding its pathogenesis,optimal treatment,and prognosis.Patients with hepatic pseudolymphoma often present non-specific clinical and imaging features,without specific tumor markers.The diagnosis of this disease mainly depends on postoperative pathological and immunohistochemical evaluations and genetic examination;timely and complete surgical resection is currently the most important treatment.
作者
于宽勇
江春平
Kuan-Yong Yu;Chun-Ping Jiang(Department of Hepatobiliary Surgery,Drum Tower Clinical Medical College,Nanjing Medical University (Nanjing Drum Tower Hospital),Nanjing 210008,Jiangsu Province,China)
出处
《世界华人消化杂志》
CAS
2019年第2期107-111,共5页
World Chinese Journal of Digestology
基金
国家自然科学基金资助项目
Nos.81572393
81602093
江苏省自然科学基金青年基金资助项目
No.BK20160118~~