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淋巴瘤样肉芽肿病(lymphomatoid granulomatosis,LYG)是极罕见全身性疾病。临床表现复杂,部位多变,浸润范围不定是诊治的难题。本文分析报告2例经病理诊断LYG的临床资料。1资料与方法1.1一般资料本院2000年3月至2002年3月收治LYG患者男、女各1例;分别为68和61岁;反复咳嗽,咯痰6
Lymphomatoid granulomatosis (LYG) is a very rare systemic disease. Complex clinical manifestations, site changes, infiltration of uncertain range is the diagnosis and treatment problems. This article analyzes the report of 2 cases of pathological diagnosis of LYG clinical data. 1 Materials and Methods 1.1 General Information The hospital from March 2000 to March 2002 LYG patients admitted to the male and female 1 case; 68 and 61 years old; repeated cough, expectoration 6