Tashiro Takashi, Uwamori Fumihiro, Nakade Yukiomi, Inoue Tadahisa, Kobayashi Yuji, Ohashi Tomohiko, Yoneda Masashi
Division of Gastroenterology, Department of Internal Medicine, Aichi Medical University, Nagakute, Japan.
Case Rep Gastroenterol. 2019 Feb 13;13(1):58-65. doi: 10.1159/000495604. eCollection 2019 Jan-Apr.
Gastrointestinal stromal tumors (GISTs) are known to originate specifically from the intestinal cells of Cajal located in the gastrointestinal mesenchyme. GISTs developing outside of the digestive tract have barely been reported. We encountered a first case of large primary GISTs in the liver with cystic changes. A 63-year-old man with a past history of brain infarction visited our hospital. The computed tomography (CT) revealed a 6-cm and a 10-cm mass in the right and the caudal lobe of the liver, respectively. These tumors have marginal enhancement in the arterial phase; however, they presented as hypodense in the internal tumor sites. Both liver tumors had cystic changes. Gastrointestinal examinations using endoscopy revealed no other gastrointestinal tumors, and [F]-fluoro-2-deoxy-D-glucose positron emission tomography/CT revealed multiple bone metastases in addition to the liver tumors. The liver tumor specimens were composed of spindle cells, and the immunohistochemical staining for c-Kit and for DOG1, as discovered on GIST, was positive. The patient was diagnosed with primary hepatic GIST with cystic changes.
胃肠道间质瘤(GISTs)已知具体起源于位于胃肠道间充质的Cajal肠细胞。消化道外发生的GISTs鲜有报道。我们遇到了首例肝脏原发性大GISTs伴囊性变的病例。一名有脑梗死病史的63岁男性前来我院就诊。计算机断层扫描(CT)显示肝脏右叶和尾叶分别有一个6厘米和一个10厘米的肿块。这些肿瘤在动脉期有边缘强化;然而,肿瘤内部呈低密度。两个肝脏肿瘤均有囊性变。内镜检查未发现其他胃肠道肿瘤,[F]-氟-2-脱氧-D-葡萄糖正电子发射断层扫描/CT显示除肝脏肿瘤外还有多处骨转移。肝脏肿瘤标本由梭形细胞组成,GIST中发现的c-Kit和DOG1免疫组化染色呈阳性。该患者被诊断为原发性肝GIST伴囊性变。