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郎格罕细胞组织细胞增生症——附1例报告及文献复习 被引量:3

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摘要 目的提高对郎格罕细胞组织细胞增生症(LCH)的认识方法报告1例LCH的病理诊断并复习文献结果光镜下形态学观察,结合免疫组化可明确诊断LCH结论病理检查是确诊郎格罕细胞组织细胞增生症的可靠手段。
出处 《罕少疾病杂志》 2007年第3期43-44,共2页 Journal of Rare and Uncommon Diseases
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参考文献5

  • 1Lichtanstein L.Histiocytosis X:integration of eosinophilic Granuloma of bone,"letterer-Siwe disease"and "Schuller Christian disease"as related manifestations of a single nosologic entity[J].Arch Pathol,1953,56:84~102. 被引量:1
  • 2Favara BE,Feller AC,PauliM.et al.Contemporary classification of histiocytic disorders[J] Med Pediatr Oncol,1997,29:157~166. 被引量:1
  • 3Scappaticc S,Danesino C,Rossi E,et al.Cytogenetic abnormalities in PHA-stimulated Lymphoeytes from patients with Langerhans cell historytosis[J],Br J Haematol,2002,111(1):252~262. 被引量:1
  • 4刘惠敏,何金,李玉莉,余宏宇,孙静,夏春燕,葛军辉.骨郎格汉斯细胞组织细胞增生症临床病理及免疫组化研究[J].第二军医大学学报,2004,25(6):646-648. 被引量:3
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二级参考文献5

  • 1[1]Favara BE, Feller AC,Pauli M,et al. Contemporary classification of histiocytic disorders. The WHO Committee On Histiocytic/Reticulum Cell Proliferations. Reclassification Working Group of the Histiocyte Society[J]. Med Pediatr Oncol, 1997,29(3):157-166. 被引量:1
  • 2[2]Kilpatrick SE,Wenger DE,Gilchrist GS,et al. Langerhans cell histiocytosis (histiocytosis X ) of bone. A clinicopathologic analysis of 263 pediatric and adult cases[J]. Cancer, 1995,76(12) :2471-2483. 被引量:1
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  • 4[4]Ghosal N,Kapila K,Kakkar S,et al. Langerhans cell histiocytosis infiltration in cerebrospinal fluid :a case report[J]. Diagn Cytopathol,2001,24(2) : 123-125. 被引量:1
  • 5[5]Fleming MD,Pinkus JL,Alexander SW,et al. Coincident expression of the chemokine receptors CCR6 and CCR7 by pathologic Langerhans cells in Langerhans cell histiocytosis[J ]. Blood, 2003,1 01 (7): 2473-2475. 被引量:1

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