罕少疾病杂志
罕少疾病雜誌
한소질병잡지
JOURNAL OF RARE AND UNCOMMON DISEASES
2014年
5期
35-37
,共3页
张学辉%万仁强%肖平%刘华盛
張學輝%萬仁彊%肖平%劉華盛
장학휘%만인강%초평%류화성
淋巴结炎%组织细胞%坏死
淋巴結炎%組織細胞%壞死
림파결염%조직세포%배사
Lymphadenitis%Histocyte%Necrosis
目的:结合文献探讨组织细胞性坏死性淋巴结炎的临床特征。方法报道2例组织细胞性坏死性淋巴结炎病例,并就本病的临床生物学特征、病因病理、诊断与鉴别诊断、治疗及预后进行分析。结果组织细胞性坏死性淋巴结炎是一种以细胞凋亡为病理特征的非特异性临床表现的淋巴系疾病。以区域性淋巴结肿大为主,易误诊。结论病理学诊断是唯一可靠依据。糖皮质激素治疗可见显著效果并缩短病程,抗生素和抗结核药物治疗无效。本病为自限性疾病,自然病程数周或数月,多数预后良好。
目的:結閤文獻探討組織細胞性壞死性淋巴結炎的臨床特徵。方法報道2例組織細胞性壞死性淋巴結炎病例,併就本病的臨床生物學特徵、病因病理、診斷與鑒彆診斷、治療及預後進行分析。結果組織細胞性壞死性淋巴結炎是一種以細胞凋亡為病理特徵的非特異性臨床錶現的淋巴繫疾病。以區域性淋巴結腫大為主,易誤診。結論病理學診斷是唯一可靠依據。糖皮質激素治療可見顯著效果併縮短病程,抗生素和抗結覈藥物治療無效。本病為自限性疾病,自然病程數週或數月,多數預後良好。
목적:결합문헌탐토조직세포성배사성림파결염적림상특정。방법보도2례조직세포성배사성림파결염병례,병취본병적림상생물학특정、병인병리、진단여감별진단、치료급예후진행분석。결과조직세포성배사성림파결염시일충이세포조망위병리특정적비특이성림상표현적림파계질병。이구역성림파결종대위주,역오진。결론병이학진단시유일가고의거。당피질격소치료가견현저효과병축단병정,항생소화항결핵약물치료무효。본병위자한성질병,자연병정수주혹수월,다수예후량호。
Objective To study the clinical characteristics of histocytic necrotizing lymphadenitis (HNL) and to review the correlative literatures.Methods Two patients admitted to our hospital were retrospectively studied, including the clinical features, histopathology, diagnosis, therapy and prognosis.Results HNL is a kind of disease of lymph system, and lymphadenopathy was the most common clinical manifestation. The pathology feature is cell apoptosis. It tends to be misdiagnosed.Conclusion The only diagnosis evidence is pathology diagnosis to HNL. Glucocorticord has better effect on HNL and can shorten the course of this disease. Those medicines of antibiotics and anti-tuberculosis have no therapeutic effect. HNL is a self-limited disease and has relatively well prognosis.