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恶性小汗腺汗孔瘤的免疫组化和超微结构观察 被引量:3

Immnohistochemical and Ultrastructural Observation on Malignant Eccrine Poroma.
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摘要 目的观察细胞角蛋白在恶性小汗腺汗孔瘤中的表达,以期探讨其组织发生。方法采用免疫组化方法对6例恶性小汗腺汗孔瘤的石蜡包埋标本进行检测,并对其中2例进行透射电镜观察。结果绝大多数肿瘤细胞示34βE12阳性,部分肿瘤细胞(衬于导管样结构和囊状腔隙内的细胞)示35βH11、CAM5.2和PKK1阳性。电镜下可见肿瘤细胞胞质内管样结构。结论证实了恶性小汗腺汗孔瘤来源于小汗腺导管。同时提示,部分肿瘤细胞显示向小汗腺分泌部分化特征。 Objective To analyze cytokeratin expressions in malignant eccrine poroma in hopes of investigating its histogenesis.Methods 6 paraffin embedded samples of malignant eccrine poroma were studied immunohistochemically,and 2 cases were observed by TEM.Results Most tumor cells showed positive reaction for 34βE 12 .Some tumor cells (lining the ductal structures and cystic spaces)revealed positive staining for 35βH 11 ,CAM5.2 and PKK 1.Intracytoplasmic cavities were observed ultrastructurally.Conclusion Our findings inferred that malignant eccrine poroma derived from errine duct,and some tumor cells differentiated towards ecrrine secretory portion.
出处 《中国皮肤性病学杂志》 CAS 北大核心 1999年第3期135-136,共2页 The Chinese Journal of Dermatovenereology
关键词 恶性 小汗腺汗孔瘤 细胞角蛋白 免疫组织化学 Malignant eccrine poroma Cytokeratin Immunohistochemistry Microscopy,electron
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  • 1孙建方,刘季和,邸晓丹,曾学思,高新元,李阿梅,桑红桂.皮脂腺痣、大汗腺痣及生乳头汗管囊腺瘤同时并发1例[J].临床皮肤科杂志,1995,24(4):244-244. 被引量:10
  • 2Sahin MT,Türel A,Gündüz K,et al.Malignant eccrine poroma in an unusual location.J Eur Acad Dermatol Venereol,2002,16(6):631-633.
  • 3Lever WF.Schaumburg-Lever C.Histopathology of the Skin[M].7th ed.London:Lippncott 1990.613
  • 4Sahin MT.Turel A.Gunduz K,et al.Malignant eccrine porma in an unusual loeation[J].J Eur Aead Dermatol Venerol.2002,16(6):631-633
  • 5Barzi AS,Ruggeri S.Recohia F,et al.Maligmant metastatic eccrine poroma.Proposal for a new therapeutic protocol[J].Dermatol Surg,1997,23(4):267-272
  • 6Gu LH, Ichiki Y, Kitajima Y. Aberrant expression of p16 and RB protein in eccrine porocarcinoma[J]. J Cutan Pathol, 2002,29(8): 473-479.
  • 7Akalin T, Sen S, Yuceturk A, et al. p53 protein expression in eccrine poroma and porocarcinoma[J]. Am J Dermatopathol, 2001,23(5): 402-406.

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