Lim Hyun Jae, Kang Hye Seon, Lee Jeong Eun, Min Ji Hye, Shin Kyung Sook, You Sun Kyoung, Kim Kyung-Hee
Department of Radiology, Chungnam National University Hospital, Daejeon 35015, South Korea.
Department of Radiology, Chungnam National University Hospital, Chungnam National University College of Medicine, Daejeon 35015, South Korea.
World J Clin Cases. 2021 May 6;9(13):3102-3113. doi: 10.12998/wjcc.v9.i13.3102.
Sarcomatoid carcinoma of the pancreas is extremely rare and has an extremely poor prognosis. Although a few cases of sarcomatoid carcinoma of pancreas have been reported, most are focused on a histopathological review. To the best of our knowledge, there are no reports documenting multimodality imaging characteristics and chronological changes with emphasis on radiologic features.
A 64-year-old woman was admitted to Chungnam National University Hospital with acute appendicitis. Contrast-enhanced computed tomography of the abdomen revealed a 2.6 cm × 2.8 cm multilobular cystic mass in the pancreatic tail. The pancreatic lesion showed suspected mural nodules and thin septa. Hence, mucinous cystic neoplasm of pancreas was considered. After 7 mo, the patient was readmitted for repeated epigastric abdominal pain and nausea. Follow-up contrast-enhanced computed tomography of the abdomen and magnetic resonance imaging revealed a marked enlargement (5.4 cm × 4 cm), with a predominant internal solid component. The mass showed low signal intensity on a T1-weighted image and heterogeneously intermediate high signal intensity on a T2-weighted image. It showed diffusion restriction and peripheral rim enhancement on an arterial phase image, and progressive enhancement on portal venous and delayed phase images. Distal pancreatectomy was performed. Based on the morphology and immunohistochemical staining of the specimen, pancreatic sarcomatoid carcinoma was diagnosed.
We present the computed tomography, magnetic resonance imaging, and positron emission tomography computed tomography findings, pathologic features, and chronological changes for preoperative diagnosis.
胰腺肉瘤样癌极为罕见,预后极差。尽管已有少数胰腺肉瘤样癌病例报告,但大多数集中在组织病理学检查。据我们所知,尚无关于多模态成像特征及时间变化(着重于放射学特征)的报告。
一名64岁女性因急性阑尾炎入住忠南国立大学医院。腹部增强计算机断层扫描显示胰尾部有一个2.6 cm×2.8 cm的多叶囊性肿块。胰腺病变显示可疑的壁结节和薄分隔。因此,考虑为胰腺黏液性囊性肿瘤。7个月后,患者因反复上腹部疼痛和恶心再次入院。腹部增强计算机断层扫描和磁共振成像随访显示肿块明显增大(5.4 cm×4 cm),内部以实性成分为主。肿块在T1加权图像上呈低信号强度,在T2加权图像上呈不均匀中等高信号强度。在动脉期图像上显示弥散受限和周边环形强化,在门静脉期和延迟期图像上呈渐进性强化。行远端胰腺切除术。根据标本的形态学和免疫组化染色,诊断为胰腺肉瘤样癌。
我们展示了计算机断层扫描、磁共振成像和正电子发射断层扫描计算机断层扫描的结果、病理特征以及术前诊断的时间变化。