期刊文献+

甲状腺Langerhans细胞组织细胞增生症的超声声像图表现

Ultrasound imaging of Langerhans cell histiocytosis involving thyroid
原文传递
导出
摘要 目的探讨甲状腺Langerhans细胞组织细胞增生症(LCH)的超声声像图表现。方法回顾性分析5例甲状腺LCH患者甲状腺超声声像图表现,其中4例患者经病理学诊断,1例为临床诊断。结果甲状腺LCH超声声像图表现为:(1)甲状腺明显增大,弥漫回声减低,不均匀,边界清或不清,彩色多普勒血流成像(CDFI):内见丰富血流信号;(2)甲状腺内见大小不等的结节样、片状和条状低回声,与正常甲状腺组织边界清,CDFI:内未见血流信号。结论甲状腺LCH超声声像图无特异性,主要表现为明显增大、弥漫回声减低且不均匀。超声引导下细针抽吸细胞学检查对诊断甲状腺LCH有帮助,但诊断率低。 Objective To investigate the ultrasound imaging of Langerhans cell histiocytosis involving thyroid. Methods Ultrasound imaging findings of five Langerhans cell histiocytosis involving thyroid were analyzed retrospectively, 4 were diagnosed by pathology, and 1 was diagnosed through clinical manifestations. Results Two types of ultrasound imaging were observed in Langerhans cell histiocytosis of thyroid:(1) The thyroid was significantly enlarged, presented diffuse and heterogenous hypoechogenicity with clear or unclear border. Color Doppler flow imaging(CDFI) showed abundant flow imaging.(2) Hypoechoic nodules, flakes and strips in varying sizes were distributed in the thyroid with clear boundary between the foci and normal gland tissue. No blood flow signal was found within hypoechogenicity. Conclusions There is no specific ultrasonographic features of Langerhans cell histiocytosis involving thyroid. The general sonographic finding is the significantly enlarged thyroid, with diffuse and heterogenous hypoechogenicity. Fine needle aspiration is useful for the diagnosis, however, the diagnostic rate is low.
出处 《中华医学超声杂志(电子版)》 2014年第8期42-45,共4页 Chinese Journal of Medical Ultrasound(Electronic Edition)
关键词 甲状腺 细胞增殖 超声检查 Thyroid gland Cell proliferation Ultrasonography
  • 相关文献

参考文献14

  • 1Hung CS, Yeh YC, Chen JC, et al. Isolated Langerhans cell histiocytosis of the thyroid in a female infant [J]. Eur J Pediatr, 2007, 166(11): 1151-1153.
  • 2Velez-Yanguas MC, Warrier RP. Langerhans' cell histiocytosis [J]. Orthop Clin North Am, 1996, 27(3): 615-623.
  • 3张嘉,王旖旎,王昭.朗格汉斯细胞源性肿瘤研究进展[J].中国实验血液学杂志,2012,20(4):1042-1046. 被引量:3
  • 4D' Ambrosio N, Soohoo S, WarshaU C, et al. Craniofacial and intracranial manifestations of langerhans cell histiocytosis: Report of findings in 100 patients [J]. AJRAm J Roentgenol, 2008,191(2): 589-597.
  • 5Avery ME, McAfee JG, Guild HG. The course and prognosis of reticuloendotheliosis (eosinophilic granuloma, Schuller-Christian disease and Letterer-Siwe disease): a study of forty cases [J]. Am J Med, 1957, 22(4): 636-652.
  • 6Lichtenstein L. Histiocytosis X: integration of eosinophilic granuloma of bone, Letterer-Siwe disease, and Schialler-Christian disease as related manifestation of a single nosologlc entity [J]. AMA Arch Pathol, 1953, 56(1): 84-102.
  • 7Lieberman PH, Jones CR, Steinman RM, et al. Langerhans cell (eosinophilic) granulomatosis. A clinicopathologic study encompassing 50 years [J]. Am J Surg Pathol, 1996, 20(5): 519-552.
  • 8Patten DK, Wain Z, Tolley N. Solitary langerhans histiocytosis of the thyroid gland: a case report and literature review [J]. Head Neck Pathol, 2012, 6(2): 279-289.
  • 9Elliott DD, Sellin R, Egger J, et al.Langerhans cell bistiocytosis presenting as a thyroid gland mass [J]. Ann Diagn Pathol, 2005, 9(5): 267-274.
  • 10Foulet-Roge A, Josselin N, Guyetant S, et al.Incidental Langerhans cell histiocytosis of thyroid: case report and review of the literature [J]. Endocr Pathol, 2002, 13(3): 227-233.

二级参考文献36

  • 1Langfort R,Radzikowska E,Czarnowska E,et al.Langerhans cellsarcoma with pulmonary manifestation,mediastinum involvementand bronchoesophageal fistula.A rare location and difficulties inhistopathological diagnosis.Pneumonol Alergol Pol,2009;77(3):327-334.
  • 2Kasper EM,Aguirre-Padilla DH,Alter RY,et al.Histiocytosis X:Characteristics,behavior,and treatments as illustrated in a caseseries.Surg Neurol Int,2011;2:57.
  • 3Cochrane LA,Prince M,Clarke K.Langerhans'cell histiocytosisin the paediatric population:presentation and treatment of head andneck manifestations.J Otolaryngol,2003;32(1):33-37.
  • 4Nicholson HS,Egeler RM,Nesbit ME.The epidemiology ofLangerhans cell histiocytosis.Hematol Oncol Clin North Am,1998;12(2):379-384.
  • 5Garabedian L,Struyf S,Opdenakker G,et al.Langerhans cellhistiocytosis:a cytokine/chemokine-mediated disorder?EurCytokine Netw.2011,22(3):148-153.
  • 6Leenen PJ,Egeler RM.Langerhans'cell histiocytosis is caused bydysregulation of the E-cadherin-beta-catenin cascade:a hypothesis.Immunol Cell Biol,1999;77(5):460-467.
  • 7Jeziorski E,Senechal B,Molina TJ,et al.Herpes-virus infectionin patients with Langerhans cell histiocytosis:a case-controlledsero-epidemiological study,and in situ analysis.PLoS One,2008;23;3(9):e3262.
  • 8Szturz P,Rˇehák Z,KoukalováR,et al.Measuring diffusemetabolic activity on FDG-PET/CT:new method for evaluatingLangerhans cellhistiocytosis activity in pulmonary parenchyma.Nucl Med Biol,2012;39(3):429-436.
  • 9Chikwava K,Jaffe R.Langerin(CD207)staining in normal pediatrictissues,reactive lymphnodes,and childhood histocytic disorders.Pediatr Dev Pathol,2004;7(6):607-614.
  • 10Weitzman S,Wayne AS,Arceci R,et al.Nucleoside analogues inthe therapy of Langerhans cell histiocytosis:a survey of members ofthehistiocyte society and review of the literature.Med PediatrOncol,1999;33(5):476-481.

共引文献2

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