DIAGNOSTIC AND THERAPEUTIC MANAGEMENT FOR LEIOMYOMA OF THE UPPER GASTROINTESTINAL TRACT

V. Shaprynskyi, Y. V. Babii
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Abstract

Summary. Leiomyoma is the most common type of mesenchymal tumor in the esophagus (70-80 %) and the second most common type of mesenchymal tumor (about 45 %) in the stomach. But in the last 20 years, we can find only a small number of publications devoted to them. And in it the leiomyoma mainly became the subject of differential-diagnostic comparison when evaluating other subepithelial neoplasms. Aim. Based on our own experience of treating patients with leiomyoma of the upper gastrointestinal tract, as well as being guided by current clinical recommendations related to the diagnosis and treatment of SEP, we will develop a diagnostic and therapeutic algorithm that will help to optimize the management tactics of patients with leiomyoma of the upper gastrointestinal tract. Materials and methods. After the analysis of the results of the treatment of 36 patients with confirmed leiomyoma of the esophagus, stomach and duodenum, a diagnostic and treatment algorithm was proposed, and it is a synthesis of our own experience and current global recommendations of such organizations as ESGE, ESMO, NCCN, JGCA, CSCO. Results. The management of leiomyoma will depend of the size of the neoplasm at the time of initial diagnosis. Taking into account the specifics of the clinical situation, an active or passive treatment strategy can be used in each individual case. The most effective methods of diagnosis and methods of surveillance are EGDS and EUSG. When choosing the surgical intervention, preference is given to endoscopic resection or laparoscopic resection. Postoperative determination of the etiology of the SEL is carried out by performing pathomorphological and immunohistochemical diagnostics. Within their histological type, leiomyoma may be characterized by a certain pathohistological pleomorphism, and are divided into leiomyoma of simple and proliferating clinical - morphological variants. Leiomyoma of the proliferating clinical-morphological variant have significantly higher indicators of such immunohistochemical markers as Ki-67 and CD31 in comparison with leiomyoma of a simple clinical-morphological variant. Therefore, leiomyoma of the proliferating clinical and morphological variant can reach much larger sizes. The size of the leiomyoma, in turn, has a direct proportional effect on the likelihood of complications. Conclusions. Leiomyoma are the common and heterogeneous type of subepithelial lesions that require a deep and detailed study.
上消化道平滑肌瘤的诊断与治疗
总结。平滑肌瘤是食道中最常见的间质肿瘤(70- 80%),是胃中第二常见的间质肿瘤(约45%)。但在过去的20年里,我们只能找到少数专门研究它们的出版物。其中,平滑肌瘤在评价其他上皮下肿瘤时主要成为鉴别诊断比较的对象。的目标。我们将根据自身治疗上消化道平滑肌瘤患者的经验,并以目前临床上与SEP诊断和治疗相关的建议为指导,开发一种诊断和治疗算法,有助于优化上消化道平滑肌瘤患者的治疗策略。材料和方法。在对36例确诊的食管、胃、十二指肠平滑肌瘤患者的治疗结果进行分析后,提出了一种诊断和治疗算法,该算法综合了我们自己的经验和目前全球ESGE、ESMO、NCCN、JGCA、CSCO等组织的推荐。结果。平滑肌瘤的处理取决于最初诊断时肿瘤的大小。考虑到临床情况的具体情况,可针对每个病例采用主动或被动治疗策略。最有效的诊断和监测方法是EGDS和EUSG。在选择手术干预时,优先考虑内镜切除或腹腔镜切除。术后通过病理形态学和免疫组织化学诊断来确定SEL的病因。在其组织学类型中,平滑肌瘤可具有一定的病理组织学多形性,分为单纯性和增殖性临床形态变异的平滑肌瘤。增殖型临床形态变异型平滑肌瘤的Ki-67、CD31等免疫组化指标明显高于单纯临床形态变异型平滑肌瘤。因此,临床和形态变异的增殖性平滑肌瘤可达到更大的尺寸。反过来,平滑肌瘤的大小与并发症的可能性成正比。结论。平滑肌瘤是一种常见且异质性的上皮下病变,需要深入细致的研究。
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