Katayama Hokahiro, Azuma Kyohei, Koneri Kenji, Murakami Makoto, Hirono Yasuo, Hatta Satomi, Imamura Yoshiaki, Goi Takanori
1st Department of Surgery, University of Fukui, 23-3 Matsuoka Shimoaiduki, Eiheiji-cho, Yoshida-gun, Fukui, Japan.
Department of Pathology, University of Fukui, 23-3 Matsuoka Shimoaiduki, Eiheiji-cho, Yoshida-gun, Fukui, Japan.
Surg Case Rep. 2020 May 24;6(1):107. doi: 10.1186/s40792-020-00869-y.
Pancreatic hamartomas are rare entities and difficult to diagnose before resection. We report a case of resected pancreatic hamartoma and literature review of typical characteristics of the lesion.
A 78-year-old man presented with a mass in his pancreas, which was incidentally identified when he experienced pneumonia. No remarkable symptoms were observed, and laboratory tests showed no abnormalities, except a slight carcinoembryonic antigen elevation. Enhanced computed tomography and magnetic resonance imaging showed a well-demarcated solid mass with heterogeneous contrast that was 2 cm in size. A gradual enhancement pattern was also observed. The biopsy revealed no specific findings; therefore, surgical resection was necessitated to confirm the diagnosis. Histopathologically, ducts, acinar cells, and adipose cells without atypia were observed among abundant fibrous stroma, but islets of Langerhans and peripheral nerves were absent. An immunohistochemical examination demonstrated CD34 and c-kit positive staining in the stromal cells, S-100 positivity in the adipose cells, and a lack of elastic fibers in the duct walls. The lesion was diagnosed as a pancreatic hamartoma.
Asymptomatic pancreatic hamartomas can avoid resection. A careful consideration of imaging and appropriate immunohistochemistry of biopsy specimen may facilitate accurate diagnosis before resection. Therefore, sufficient recognition of the characteristics of pancreatic hamartomas is desirable.
胰腺错构瘤是一种罕见的病变,在切除前很难诊断。我们报告一例经手术切除的胰腺错构瘤病例,并对该病变的典型特征进行文献复习。
一名78岁男性因胰腺肿物就诊,该肿物是在他患肺炎时偶然发现的。未观察到明显症状,实验室检查除癌胚抗原略有升高外无异常。增强计算机断层扫描和磁共振成像显示一个边界清晰的实性肿物,大小为2厘米,对比增强不均匀。还观察到渐进性增强模式。活检未发现特异性结果;因此,需要手术切除以明确诊断。组织病理学检查显示,在丰富的纤维基质中观察到无异型性的导管、腺泡细胞和脂肪细胞,但未发现胰岛和周围神经。免疫组织化学检查显示,基质细胞中CD34和c-kit呈阳性染色,脂肪细胞中S-100呈阳性,导管壁中缺乏弹性纤维。该病变被诊断为胰腺错构瘤。
无症状的胰腺错构瘤可避免切除。仔细考虑影像学表现并对活检标本进行适当的免疫组织化学检查,可能有助于在切除前做出准确诊断。因此,充分认识胰腺错构瘤的特征是很有必要的。