Kuhnen C, Mentzel T, Haarmann W, Schwegler U, Sciot R, Debiec-Rychter M
Institut für Pathologie am Clemenshospital, Medical Center, Düesbergweg 128, 48153 Münster.
Pathologe. 2010 May;31(3):199-204. doi: 10.1007/s00292-009-1271-8.
Two cases of primary gastric atypical lipomatous tumors (ALT) are presented. In case No.1, a 7x4x3 cm submucosal ALT (lipoma-like subtype) of the antrum/pyloric region in a 60-year-old woman was completely resected. Using interphase dual-color-FISH, MDM2- and CDK4 amplifications could be detected in distinguished amplicons. The patient was continuously free of disease after 56 months. In case No. 2, a 3.5 cm (in diameter) submucosal ALT (lipoma-like subtype) of the gastric body in a 56-year-old woman was completely resected. FISH revealed MDM2 amplification while the CDK4 gene remained in diploid copies. This patient was continuously free of disease after 36 months. The morphologic and molecular biological findings of this rare primary gastric mesenchymal tumor are discussed in comparison with the corresponding soft tissue lesions.
本文报告了两例原发性胃非典型脂肪瘤性肿瘤(ALT)。病例1为一名60岁女性,其胃窦/幽门区有一个7×4×3 cm的黏膜下ALT(脂肪瘤样亚型),已被完整切除。通过间期双色荧光原位杂交(FISH),在不同的扩增子中检测到MDM2和CDK4基因扩增。该患者在56个月后仍无疾病复发。病例2为一名56岁女性,其胃体有一个直径3.5 cm的黏膜下ALT(脂肪瘤样亚型),也已被完整切除。FISH检测显示MDM2基因扩增,而CDK4基因保持二倍体拷贝数。该患者在36个月后仍无疾病复发。本文将这种罕见的原发性胃间质肿瘤的形态学和分子生物学发现与相应的软组织病变进行了比较讨论。