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增殖期血管瘤和卡波西样血管内皮瘤的病理比较研究 被引量:4

Comparative Study On Pathology of Proliferating Infantile Hemangioma and Kaporsiform Hemangioendothelioma
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摘要 目的正确鉴别体表软组织深部的增殖期婴幼儿血管瘤(Infantile hemangioma,IH)和卡波西样血管内皮瘤(Kaporsiform Hemangioendothelioma,KHE)是选择合适治疗方案的重要条件。从多方面比较增殖期IH和KHE的病理特征,为更准确地鉴别诊断这两种疾病提供依据。方法在2001年1月至2009年6月期间,收集21例增殖期IH和12例KHE标本。采用HE染色、透射电镜和免疫组化染色等方法,比较增殖期IH和KHE的病理结构和抗原标记(D2-40和Glut1)的表达。结果 HE染色显示,增殖期IH有众多毛细血管丛,新生毛细血管壁内可见扁平状周细胞;KHE由肿瘤结节组成,结节中心是大量狭缝状管腔,结节边缘可见毛细血管。在电镜下观察,增殖期IH的毛细血管壁基底膜呈多层板状结构,基底膜内有周细胞;KHE的狭缝状管腔和毛细血管壁基底膜仅有数层,且不连续,基底膜内也可见周细胞。增殖期IH肿瘤内皮细胞不表达D2-40,强烈表达Glut1;而KHE仅表达D2-40,不表达Glut1。结论增殖期IH的病理结构与KHE有明显差别。D2-40和Glut1可以作为鉴别增殖期IH和KHE的可靠抗原标记。 Objective To distinguish proliferating infantile hemangioma (IH) and kaporsiform hemangioendothelioma (KHE) by comparing the pathological structure and marker antigen expression. Methods From January 2001 to June 2009, 33 paraffin-embedded and fresh samples, 21 proliferating IH and 11 KHE, were collected from Nanjing Children's Hospital and Jinling Hospital. Hematoxylin-eosin (HE) staining and transmission electron microscopy (TEM) were used to observe the pathological structure. Immunohistochemical analysis was also performed to investigate the expression of D2-40 and Glutl. Results HE staining revealed that proliferating IH had dense capillary plexus and flat pericytes in the wall of neo- capillaries, and that KHE was composed of tumor nodules with slit-like channels in the center and capillaries in the margin. TEM revealed multi-layer basement membrane of neo-capllaries in IH, and slit-like channels and capillaries with thin- layered basement membrane in KHE. There were pericytes in the basement membrane in both. Immunochemistry revealed that the endothelial cells expressed Glut1, but not D2-40 in IH; while D2-40, but not Glutl in KHE. Conclusion The pathological structure of proliferating IH is obviously different from that of KHE. D2-40 and Glut1 are the reliable marker antigens for differential diagnosis of proliferating IH and KHE.
出处 《组织工程与重建外科杂志》 2010年第2期85-88,共4页 Journal of Tissue Engineering and Reconstructive Surgery
基金 国家自然科学基金项目(30700874) 中国博士后科学基金项目(20090451571) 江苏省博士后科研资助计划项目(0901062C) 南京军区南京总医院科研基金资助(2009Q038)
关键词 婴幼儿血管瘤 卡波西样血管内皮瘤 病理学 抗原标记 Infantile hemangioma Kaporsifoim hemangioendothelioma Pathology Marker antigen
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参考文献21

  • 1Chiller KG,Passaro D,Frieden IJ.Hemangiomas of infancy:clinical characteristics,morphologic subtypes,and their relationship to race,ethnicity,and sex[J].Arch Dermatol,2002,138(12):1567-1576. 被引量:1
  • 2Lyons LL,North PE,Mac-Moune LF,et al.Kaposiform hemang-ioendothelioma:a study of 33 cases emphasizing its pathologic,immunophenotypic,and biologic uniqueness from juvenile hemangioma[J].Am J Surg Pathol,2004,28(5):559-568. 被引量:1
  • 3Zukerberg LR,Nickoloff BJ,Weiss SW.Kaposiform hemangioen-dothelioma of infancy and childhood; an aggressive neoplasm associated with Kasabach-Merritt syndrome and lymphangiomatosis[J].Am J Surg Pathol,1993,7(4):321-328. 被引量:1
  • 4林晓曦.血管瘤和血管畸形:经验、进展与挑战[J].中华整形外科杂志,2007,23(2):81-83. 被引量:28
  • 5Abass K,Saad H,Kherala M,et al.Successful treatment of Kasabach-Merritt syndrome with vincristine and surgery:a case report and review of literature[J].Cases J,2008,1:9. 被引量:1
  • 6袁斯明,邢新,欧阳天祥,倪灿荣,杨志勇,张敬德.婴幼儿血管瘤病理演变过程中形态观察[J].临床与实验病理学杂志,2005,21(3):290-294. 被引量:15
  • 7Weiss SW,Goldblum JR.Hemangioendothelioma:vascular tumors of intermediate malignancy // Enzinger and Weiss's soft tissue tumors[M].St.Louis:Mosby,2001,891-915. 被引量:1
  • 8袁斯明,姜会庆,汪军,洪志坚.复方倍他米松局部注射控制性治疗婴幼儿真性血管瘤[J].中国美容整形外科杂志,2009,20(5):292-294. 被引量:4
  • 9Rodriguez V,Lee A,Witman PM,et al.Kasabach-merritt phenomenon:case series and retrospective review of the mayo clinic experience[J].J Pediatr Hematol Oncol,2009,31(7):522-526. 被引量:1
  • 10López V,Martí N,Pereda C,et al.Successful management of kaposiform hemangioendothelioma with kasabach-merritt phenomenon using vincristine and ticlopidine[J].Pediatr Dermatol,2009,26(3):365-366. 被引量:1

二级参考文献19

  • 1JIANGXue-wu WANGGuang-huan LIJian-hong CHENZhong-xian HEFei.Expression of glucocorticoid receptor isoforms in cutaneous hemangiomas and vascular malformations[J].Chinese Medical Journal,2005(12):977-981. 被引量:2
  • 2刘潜,李静,周德凯,李晓庆,唐开勇,金先庆.糖皮质激素瘤内注射治疗婴幼儿血管瘤机理的研究[J].第四军医大学学报,2007,28(13):1199-1201. 被引量:15
  • 3Chiller KG, Passaro D,Frieden IJ. Hemangiomas of infancy: clinical characteristics, morphologic subtypes, and their relationship to race, ethnicity, and sex [ J ]. Arch Dermatol, 2002,138 ( 12 ): 1567-76. 被引量:1
  • 4Boye E, Yu Y, Paranya G, et al. Clonality and altered behavior of endothelial cells from hemangiomas [ J ]. J Clin Invest, 2001,107(6) :745 -52. 被引量:1
  • 5Walter JW, North PE,Waner M,et al. Somatic mutation of vascular endothelial growth factor receptors in juvenile hemangioma[ J].Genes Chromosomes Cancer,2002,33(3 ) :295 -303. 被引量:1
  • 6Walter JW, Blei F, Anderson JL,et al. Genetic mapping of a novel familial form of infantile hemangioma[ J]. Am J Med Genet, 1999,82(1) :77 -83. 被引量:1
  • 7Blei F,Walter JW,Orlow SJ,et al. Familial segregation of hemangiomas and vascular malformations as an autosomal dominant trait [J]. Arch Dermatol 1998,134(6) :718 -22. 被引量:1
  • 8Yu Y,Flint AF,Mulliken JB,et al. Endothelial progenitor cells in infantile hemangioma [ J ]. Blood,2004,103 (4): 1373 - 75. 被引量:1
  • 9Burton BK,Schulz CJ,Angle B,et al. An increased incidence of haemangiomas in infants born following chorionic villus sampling (CVS) [J]. Prenat Diagn,1995,15(3) :209 - 14. 被引量:1
  • 10North PE, Waner M, Mizeracki A, et al. A unique microvascular phenotype shared by juvenile hemangiomas and human placenta [ J ]. Arch Dermatol,2001,137 (5) :559 - 70. 被引量:1

共引文献43

同被引文献103

  • 1马捷,石群立,周晓军,吴苏稼,姜少军,张宗军,周航波.骨卡波西样血管内皮瘤临床病理特点[J].临床与实验病理学杂志,2007,23(2):189-193. 被引量:14
  • 2Zukerberg LR, Nickoloff B J, Weiss SW. Kaposiform hemangioendothelioma of infancy and childhood. An aggressive neoplasm associated with Kasabach-Merritt syndrome and lymphangiomatosis. Am J Surg Pathol, 1993, 17: 321-328. 被引量:1
  • 3Lyons LL, North PE, Mac-Moune Lai F, et al. Kaposiform hemangioendothelioma: a study of 33 cases emphasizing its pathologic, immunophenotypic, and biologic uniqueness from juvenile hemangioma. Am J Surg Pathol, 2004, 28: 559-568. 被引量:1
  • 4Dasgupta R, Fishman SJ. ISSVA classification. Semin Pediatr Surg, 2014, 23 : 158-161. 被引量:1
  • 5Enjolras O, Wassef M, Mazoyer E, et al. Infants with Kasabach- Merritt syndrome do not have "true" hemangiomas. J Pediatr, 1997, 130: 631-640. 被引量:1
  • 6Croteau SE, Liang MG, Kozakewieh HP, et aL Kaposiform hemangioeudothelioma: atypical features and risks of Kasabach- Merritt phenomenon in 107 referrals. J Pediatr, 2013, 162: 142-147. 被引量:1
  • 7Fernandez Y, Bernabeu-Wittel M, Garcia-Morillo JS. Kaposiform hemangioendothelioma. Eur J Intern Med, 2009, 20: 106-113. 被引量:1
  • 8Nakaya T, Morita K, Kurata A, et al. Multifocal kaposiform hemangioendothelioma in multiple visceral organs: an autopsy of 9- day-old female baby. Hum Pathol, 2014, 45: 1773-1777. 被引量:1
  • 9Sarkar M, Mulliken JB, Kozakewieh HP, et al. Thrombocytopenie coagulopathy (Kasabach-Merritt phenomenon ) is associated with Kaposiform hemangioendothelioma and not with common infantile hemangioma. Plast Reeonstr Surg, 1997, 100: 1377-1386. 被引量:1
  • 10Low IC, Yang RY, Symmans PJ. Microscopic Kaposiform hemangioendothelioma with extensive lymphangiomatosis : extraordinary example of an unusual entity. Int J Surg Pathol, 2013, 21 : 297-302. 被引量:1

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