关键词: Inflammatory myofibroblastoma tumor ciliary body immunohistochemistry

Mesh : Ciliary Body / surgery Humans Immunohistochemistry Male Middle Aged Neoplasms, Muscle Tissue / diagnosis pathology surgery Uveal Neoplasms / diagnosis pathology

来  源:   DOI:10.1186/s12886-022-02411-0

Abstract:
BACKGROUND: Inflammatory Myofibroblastoma Tumors (IMTs) are extremely tumour rare in the intraocular.
METHODS: A ciliary body tumor was found under slit lamp biomicroscopy in a 55-year-old male first diagnosed with cataract. Then this patient underwent trans-sclera resection via partial lamellar sclerouvectomy and par plans vitrectomy to remove the mass. Hematoxylin and eosin (HE) staining and immunohistochemistry findings showed that the characteristics of the tumor were consistent with IMT.
CONCLUSIONS: We reported a rare case of intraocular IMT, which is confirmed by H&E staining, and IHC positive staining for Vimentin, Desmin and ALK, while negative staining for SMA, S-100, ki-67, CK, CD68, and calponin.
摘要:
背景:炎性肌纤维母细胞瘤肿瘤(IMT)是眼内极其罕见的肿瘤。
方法:在裂隙灯生物显微镜检查下,一名55岁男性首次诊断为白内障,发现睫状体肿瘤。然后,该患者通过部分板层巩膜切除术和par计划玻璃体切除术进行了巩膜切除术,以去除肿块。苏木精和伊红(HE)染色和免疫组织化学结果显示,肿瘤的特征与IMT一致。
结论:我们报道了一例罕见的眼内IMT,这是由H&E染色证实,和Vimentin的IHC阳性染色,Desmin和ALK,而SMA阴性染色,S-100,ki-67,CK,CD68和calponin。
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