期刊文献+

组织细胞增生性病变病理学特点与鉴别要点 被引量:6

The clinicopathological characteristics and differential diagnosis of histiocytosis
下载PDF
导出
摘要 组织细胞增生性病变分为组织细胞增生症X(朗格汉斯细胞组织细胞增生症)和非朗格汉斯细胞组织细胞增生症。前者好发于淋巴造血系统,常累及中枢神经系统。后者包括累及淋巴造血系统和(或)中枢神经系统的Rosai.Dorfman病、噬血细胞性淋巴组织细胞增生症、欧迪海姆.奇斯特病、幼年性黄色肉芽肿和播散性黄色瘤、脉络丛黄色肉芽肿、脉络丛黄色瘤。本文简要介绍上述组织细胞增生性病变的临床病理学特点与鉴别要点。由于其在中枢神经系统的发病率低,未能引起神经外科和病理科医师的足够重视,易造成误诊和误治。因此,了解此类疾病的临床和病理学特征有助于提高其诊断与治疗水平。 The histiocytosis is divided into Langerhans' cell histiocytosis(histiocytosis X) and non.Langerhans' cell histiocytosis(NLCH). The former mainly occurs in lymphatic hematopoietic tissue and often involves central nervous system(CNS). The latter includes Rosai. Dorfman disease(RDD),hemophagocytic lymphohistiocytosis(HLH), Erdheim. Chester disease(ECD), juvenile xanthogranuloma(JXG) and xanthoma disseminatum(XD), choroid plexus xanthogranuloma(CPXG), choroid plexus xanthoma(CPX), which may occur in lymphatic hematopoietic tissue and(or) CNS. This review has briefly introduced the clinicopathological characteristics and differential diagnosis of the above lesions. The incidence of these diseases is low in CNS, so they are often ignored, misdiagnosed and impertinently treated by neurosurgeons and pathologists. Therefore, understanding their clinical and pathological characteristics is conducive to improve the diagnosis and therapy.
作者 于士柱
出处 《中国现代神经疾病杂志》 CAS 2015年第4期256-262,共7页 Chinese Journal of Contemporary Neurology and Neurosurgery
基金 国家重点基础研究发展计划(973计划)项目(项目编号:2010CB529405) 国家自然科学基金青年科学基金资助项目(项目编号:81202102) 国家自然科学基金青年科学基金资助项目(项目编号:81402050) 天津市科技支撑计划项目(项目编号:12ZCDZSY17400) 天津市应用基础及前沿技术研究计划项目(项目编号:13JCQNJC12100) 天津市高等学校科技发展基金资助项目(项目编号:2004ZD06) 天津市高等学校科技发展基金资助项目(项目编号:20110102) 中国抗癌协会神经肿瘤专业委员会科研项目(项目编号:CSNO-2013-MSD010) 天津医科大学青年基金资助项目(项目编号:2013KYQ02) 天津医科大学青年基金资助项目(项目编号:2014KYQ02)~~
关键词 组织细胞增生症 朗格汉斯细胞 非朗格汉斯组织细胞 病理学 诊断 鉴别 Histiocytosis Langerhans cells Non-Langerhans histiocytes Pathology Diagnosis differential
  • 相关文献

参考文献9

  • 1Louis DN, Ohgaki H, Wiestler OD, Cavenee WK. WHO classification of tumors of the central nervous system. Lyon: IARC Press, 2007: 193-196. 被引量:1
  • 2Martin-Duverneuil N, Idhaih A, Hoang-Xuan K, Donadieu ], Genereau T, Guillevin R, Chiras J; French Langerhans Cell Histiocytosis Study Group. MRI features of neurodegenerative Langerhans cell histiocytosis. Eur Radiol, 2006, 16:2074-2082. 被引量:1
  • 3Grois N, Prayer D, Prosch H, Lassmann H; CNS LCH Co- operative Group. Neuropathology of CNS disease in Langerhans cell histiocytosis. Brain, 2005, 128(Pt 4):829-838. 被引量:1
  • 4Tomio R, Katayama M, Takenaka N, Imanishi T. Complications of surgical treatment of Rosai-Dorfman disease: a case report and review. Surg Neurol Int, 2012, 3:1. 被引量:1
  • 5Fukushima T, Yachi K, Ogino A, Ohta T, Watanabe T, Yoshino A, Katayama Y. Isolated intracranial Rosai- Dorfman disease without dural attachment: case report. Neurol Med Chir (Tokyo), 2011, 51:136-140. 被引量:1
  • 6Janka GE. Familial and acquired hemophagocytic lymphohistiocytosis. Annu Rev Med, 2012, 63:233-246. 被引量:1
  • 7Horne A, Trottestam H, Aricb M, Egeler RM, Filipovich AH, Gadner H, Imashuku S, Ladisch S, Webb D, Janka G, Henter JI; Histiocyte Society. Frequency and spectrum of central system involvement in 193 children with haemophagocytic lymphohistiocytosis. Br J Haematol, 2008, 140: 327-335. 被引量:1
  • 8Haroehe J, Arnaud L, Cohen-Aubart F, Hervier B, Charlotte F, Emile JF, Amoura Z. Erdheim-Chester disease. Rheum Dis Clin North Am, 2013, 39:299-311. 被引量:1
  • 9Arnaud L, Hervier B, N6el A, Hamidou MA, Kahn JE, Wechsler B, P6rez- Pastor G, Blomberg B, Fuzibet JG, Dubourguet F, Marinho A, Magnette C, Noel V, Pavic M, Casper J, Beucher AB, Costedoat- Chalumeau N, Aaron L, Salvatierra J, Graux C, Cacoub P, Delcey V, Dechant C, Bindi P, Herbaut C, Graziani G, Amoura Z, Haroche J. CNS involvement and treatment with interferon-cL are independent prognostic factors in Erdheim- Chester disease: a muhicenter survival analysis of 53 patients. Blood, 2011, 117:2778-2782. 被引量:1

同被引文献43

引证文献6

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部