CAJ | 학술논문

目的：分析小肠淋巴管瘤的临床及病理组织学特征。方法报道一例发生在小肠的病例，从临床病理及鉴别诊断方面进行探讨。结果组织学与软组织淋巴管瘤一致，免疫组化D2-40,F8,CD31,CD34阳性。结论小肠淋巴管瘤是非常罕见的良性肿瘤，临床表现为渐进性不完全肠梗阻。手术切除可治愈。
목적：분석소장림파관류적림상급병리조직학특정。방법보도일례발생재소장적병례，종림상병리급감별진단방면진행탐토。결과조직학여연조직림파관류일치，면역조화D2-40,F8,CD31,CD34양성。결론소장림파관류시비상한견적량성종류，림상표현위점진성불완전장경조。수술절제가치유。
Objective: to analyze the clinical and pathologic features of lymphangioma of intestine.Methods: report of one case occurred in the smal intestine of the case, carries on the discussion from the aspects of clinical pathological features and differential diagnosis.Results: histological and soft tissue tumor, immunohistochemistry of D2-40, F8, CD31, CD34 positive Conclusion: intestinal lymphatic tumor is very rare benign tumor, clinical manifestations of progressive incomplete intestinal obstruction. Operation resection can be cured.