Han Sang Hoon, Park Se Hoon, Cho Gwon Hyun, Kim Na Rae, Oh Jae Hwan, Nam Eunmi, Shin Dong Bok
Department of Internal Medicine, Gachon Medical School, Gil Medical Center, Incheon, Korea.
Korean J Intern Med. 2007 Mar;22(1):21-3. doi: 10.3904/kjim.2007.22.1.21.
Neurofibromatosis type 1 (von Recklinghausen's disease, NF-1) is an autosomal-dominant neurocutaneous disorder characterized by abnormal skin pigmentation (café au lait spots and axillary freckling), cutaneous and plexiform neurofibromas, skeletal dysplasias, and Lisch nodules (pigmented iris hamartomas). Gastrointestinal stromal tumors (GISTs) are the most common tumors of mesenchymal origin in the gastrointestinal tract, mesentery, omentum, and retroperitoneum. Here, we report a case of GIST in the ileum of a 76-year-old woman previously diagnosed as NF-1. She was admitted due to sudden onset of abdominal pain. Contrast enhanced CT scan revealed a moderately defined, peripherally enhanced soft tissue mass of about 8.8 x 7.3cm, originating from the small bowel in the left of the abdomen. Surgical excision was performed and the tumor was found to be composed of tumor cells that were positive for c-kit protein. The patient started imatinib treatment a month later, but stopped medication due to dyspepsia after a few months and eventually progressed after 18 months.
1型神经纤维瘤病(冯雷克林霍增氏病,NF-1)是一种常染色体显性神经皮肤疾病,其特征为皮肤色素沉着异常(牛奶咖啡斑和腋窝雀斑)、皮肤和丛状神经纤维瘤、骨骼发育异常以及Lisch结节(色素性虹膜错构瘤)。胃肠道间质瘤(GIST)是胃肠道、肠系膜、网膜和腹膜后最常见的间充质起源肿瘤。在此,我们报告一例76岁先前诊断为NF-1的女性回肠GIST病例。她因突发腹痛入院。增强CT扫描显示一个边界中度清晰、周边强化的软组织肿块,大小约8.8×7.3cm,起源于腹部左侧的小肠。进行了手术切除,发现肿瘤由c-kit蛋白阳性的肿瘤细胞组成。患者一个月后开始接受伊马替尼治疗,但几个月后因消化不良停药,最终在18个月后病情进展。