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1972年Liebow等首先提出淋巴肉芽肿是一种特殊的临床病理实体,呈多形态血管侵袭性和坏死性的淋巴网状系统的浸润。早期淋巴肉芽肿最常损害肺、皮肤、肾间质和中枢神经系统。临床上2/3病例死亡,中数生存期为14月。文献曾报告淋巴肉芽肿系多克隆B细胞增殖,进而可发展为B-细胞淋巴瘤。而本文报告1例经免疫学研究证实为T-细胞增殖的淋巴肉芽肿。患者男性,29岁。3个月前因鼻分泌物增多、干咳和全身不适而入院。胸部X片诊断为霉菌感染,应
In 1972, Liebow et al. First proposed that lymphatic granuloma is a special clinicopathologic entity that is infiltrated by multi-morphologically invasive and necrotic lymphoreticular systems. Early lymphatic granulomas most often damage lungs, skin, renal interstitium and the central nervous system. Clinically, 2/3 of the cases died, the median survival was 14 months. The literature has reported that lymphoid granuloma polyclonal B cell proliferation, which can be developed into B-cell lymphoma. This article reports 1 case of lymphogranuloma confirmed by immunological studies as T-cell proliferation. Patient male, 29 years old. 3 months ago due to increased nasal secretions, dry cough and general malaise and hospitalization. Chest X-ray diagnosis of mold infection should be