Monomorphic epitheliotropic intestinal T-cell lymphoma: A clinic-pathologic study of 3 cases and literature review
10.11855/j.issn.0577-7402.2018.01.09
- VernacularTitle:单形性嗜上皮性肠道T细胞淋巴瘤3例报道与文献复习
- Author:
Li WANG
1
;
De-Hong HUANG
;
Chun-Yan XIAO
;
Yu LI
;
Wen-Jun ZHANG
;
Bing-Lin GUO
;
Yi GONG
;
Tao YANG
;
Qi-Ying LI
;
Yin-Yu NAN
;
Jun ZHANG
;
Ying XIANG
Author Information
1. 400030重庆,重庆大学附属肿瘤医院、重庆市肿瘤研究所、重庆市肿瘤医院血液肿瘤科
- Keywords:
monomorphicepitheliatropic intestinal t-cell lymphoma;
diagnosis;
therapy
- From:
Medical Journal of Chinese People's Liberation Army
2018;43(1):45-50
- CountryChina
- Language:Chinese
-
Abstract:
Objective To summarize the clinicopathological features of monomorphic epitheliotropic intestinal T cell lymphoma (MEITL),and provide the experiences and lessons for diagnosis and treatment.Methods The clinical manifestations,histopathological and immunohistochemical characteristics,diagnosis,treatment and prognosis of 3 cases of MEITL were analyzed retrospectively.Meanwhile,the other cases published in the literatures were reviewed and summarized.Results Two cases of middle aged and aged men and one young woman were reported in present paper.These lesions of all the 3 patients were at the small intestine,of which the female patients had skin and mammary gland involvement.The clinical manifestations were abdominal distention,mulligrubs and intestinal perforation,and the main pathological feature was the diffuse infiltration of the homogeneous tumor cells in the whole layer intestinal wall.Immunohistochemical examination showed that tumor cells expressed all T cell markers CD3,CD8,CD56,T cell cytoplasmic antigen (TIA-1),CD4 and CD5,and Ki-67 proliferation index was 50％-70％.As to the treatment,case 1 received CHOP and GDP regimens successively,and died 2 years after final diagnosis.Case 2 received CHOP regimen for 1 course of chemotherapy and died of giving up treatment.Case 3 gave up treatment,voluntary discharged and then lost.It is clear according to the previous literatures and our experiences that the MEITL possesses high invasiveness and low incidence,and makes the diagnosis difficult;the patient's response to the current treatment is poor.Conclusions MEITL is prone to be in the small intestine.The diagnosis of MEITL should be based on clinical manifestations,pathological features and immunohistochemical detection results.MEITL is rare,the course of disease progresses rapidly,and the patients have the tendency to have intestinal perforation and poor prognosis.Early diagnosis and positive chemotherapy may lead to a better prognosis.
