Eyden Brian, Chorneyko Katherine A, Shanks Jonathan H, Menasce Lia P, Banerjee S Sankar
Department of Histopathology, Christie Hospital, Manchester, United Kingdom.
Ultrastruct Pathol. 2002 Sep-Oct;26(5):269-85. doi: 10.1080/01913120290104548.
Eighty-two mesenchymal tumors of the gastrointestinal tract were examined by electron microscopy for the purposes of subtyping for diagnostic precision and of understanding cellular differentiation. Tumors were subclassified into leiomyoma/leiomyosarcoma, tumors of the interstitial cell of Cajal (equivalent to traditionally defined GISTs [Miettinen et al. Hum Pathol. 1999; 30:1213-1220; Mod Pathol. 2000; 13:1134-1142]), gastrointestinal autonomic nerve tumors (GANTs), and fibroblastic and myofibroblastic tumors, using criteria from the literature. Leiomyoma/leiomyosarcoma were diagnosed by myofilaments, attachment plaques, plasmalemmal caveolae, and lamina; GIST by processes or cell bodies full of intermediate filaments, solitary focal densities amid intermediate filaments, attachment plaques with incomplete lamina, scarce myofilaments, and smooth endoplasmic reticulum; GANTs by neuroendocrine granules, cell bodies/processes full of intermediate filaments (more rarely microtubules), and smooth endoplasmic reticulum; fibroblastic/myofibroblastic tumors by abundant rough endoplasmic reticulum, myofilaments, and fibronexuses. Seventy-three tumors (89%) were successfully subclassified, as 5 leiomyoma/leiomyosarcoma (6%), 36 GISTs (44%), 22 GANTs (27%), 10 fibroblastic and myofibroblastic tumors (12%). Results indicated overlap between poorly differentiated leiomyosarcoma and GIST, and between GIST and GANT. GANT is emphasized as a neuronal tumor identifiable by electron microscopy, and thereby distinguishable from GIST.
为提高诊断准确性及了解细胞分化情况,对82例胃肠道间叶性肿瘤进行了电镜检查。根据文献标准,将肿瘤分为平滑肌瘤/平滑肌肉瘤、 Cajal间质细胞瘤(等同于传统定义的胃肠道间质瘤[Miettinen等人,《人类病理学》。1999年;30:1213 - 1220;《现代病理学》。2000年;13:1134 - 1142])、胃肠道自主神经肿瘤(GANTs)以及成纤维细胞和肌成纤维细胞肿瘤。平滑肌瘤/平滑肌肉瘤通过肌丝、附着斑、质膜小窝和板层进行诊断;胃肠道间质瘤通过充满中间丝的突起或细胞体、中间丝中的孤立局灶性致密物、带有不完整板层的附着斑、稀少的肌丝和平滑内质网进行诊断;胃肠道自主神经肿瘤通过神经内分泌颗粒、充满中间丝(较少见微管)的细胞体/突起和平滑内质网进行诊断;成纤维细胞/肌成纤维细胞肿瘤通过丰富的粗面内质网、肌丝和纤维连接进行诊断。73例肿瘤(89%)成功分类,其中5例为平滑肌瘤/平滑肌肉瘤(6%),36例为胃肠道间质瘤(44%),22例为胃肠道自主神经肿瘤(27%),10例为成纤维细胞和肌成纤维细胞肿瘤(12%)。结果表明,低分化平滑肌肉瘤与胃肠道间质瘤之间以及胃肠道间质瘤与胃肠道自主神经肿瘤之间存在重叠。强调胃肠道自主神经肿瘤是一种可通过电镜识别的神经肿瘤,从而与胃肠道间质瘤相区分。