Yoshihiro Tomoyasu, Nio Kenta, Tsuchihashi Kenji, Ariyama Hiroshi, Kohashi Kenichi, Tsuruta Nobuhiro, Hanamura Fumiyasu, Inadomi Kyoko, Ito Mamoru, Sagara Kosuke, Okumura Yuta, Nakano Michitaka, Arita Shuji, Kusaba Hitoshi, Oda Yoshinao, Akashi Koichi, Baba Eishi
Department of Hematology and Oncology, Kyushu University Hospital, Fukuoka 812-8582, Japan.
Department of Anatomical Pathology, Pathological Sciences, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.
Mol Clin Oncol. 2017 Jun;6(6):866-870. doi: 10.3892/mco.2017.1240. Epub 2017 May 5.
Pancreatic acinar cell carcinoma (PACC) is a rare tumor of the exocrine pancreas, representing only 1% of all pancreatic malignancies. A 50-year-old man presented with edema of the thumb joints bilaterally, followed by an appearance of masses in the bilateral lower extremities and fever (38°C). The masses were diagnosed as panniculitis by skin biopsy, and multiple intraperitoneal masses were incidentally detected on pelvic magnetic resonance imaging performed to investigate the leg abnormalities. The patient was referred to the Kyushu University Hospital for further investigation, and fluorodeoxyglucose-positron emission tomography/computed tomography (CT) revealed high-uptake tumors in the pancreatic tail, in the periphery of the liver, and in the pelvis. Laboratory examinations revealed high serum concentrations of pancreatic exocrine enzymes, such as lipase, trypsin, elastase 1 and pancreatic phospholipase A2. Histological examination of a bioptic specimen obtained from a hepatic lesion revealed proliferation of atypical cells arranged in a tubular or glandular pattern. Immunohistochemical staining revealed that the atypical cells were positive for cytokeratin (CK)7, CK19 and lipase, but negative for CK20 and thyroid transcription factor-1, leading to a final diagnosis of acinar cell carcinoma of the pancreatic tail (T4bN0M1, stage IV according to the 7th edition of the TNM Classification of Malignant Tumors). Combined chemotherapy with oxaliplatin, irinotecan and fluorouracil (FOLFIRINOX) was administered and fever was soon alleviated. The serum levels of lipase also declined and panniculitis completely resolved. As of the start of the 8th course of chemotherapy, the levels of the pancreatic exocrine enzymes were within normal ranges and CT revealed partial response. Therefore, the severe lipase hypersecretion syndrome was well controlled by the FOLFIRINOX regimen and shrinkage of the mass was also achieved. Thus, the FOLFIRINOX regimen may represent an effective treatment option for advanced PACC.
胰腺腺泡细胞癌(PACC)是一种罕见的胰腺外分泌肿瘤,仅占所有胰腺恶性肿瘤的1%。一名50岁男性双侧拇指关节出现水肿,随后双侧下肢出现肿块并伴有发热(38°C)。皮肤活检将肿块诊断为脂膜炎,在为检查腿部异常而进行的盆腔磁共振成像中偶然发现多个腹腔内肿块。患者被转诊至九州大学医院进行进一步检查,氟脱氧葡萄糖-正电子发射断层扫描/计算机断层扫描(CT)显示胰尾、肝周和盆腔有高摄取肿瘤。实验室检查显示血清中胰脂肪酶、胰蛋白酶、弹性蛋白酶1和胰磷脂酶A2等胰腺外分泌酶浓度升高。对取自肝脏病变的活检标本进行组织学检查,发现非典型细胞呈管状或腺管状排列增生。免疫组化染色显示非典型细胞细胞角蛋白(CK)7、CK19和脂肪酶呈阳性,但CK20和甲状腺转录因子-1呈阴性,最终诊断为胰尾腺泡细胞癌(T4bN0M1,根据《恶性肿瘤TNM分类》第7版为IV期)。给予奥沙利铂、伊立替康和氟尿嘧啶联合化疗(FOLFIRINOX),发热很快缓解。脂肪酶血清水平也下降,脂膜炎完全消退。截至化疗第8疗程开始时,胰腺外分泌酶水平在正常范围内,CT显示部分缓解。因此,FOLFIRINOX方案很好地控制了严重的脂肪酶分泌过多综合征,肿瘤也出现缩小。因此,FOLFIRINOX方案可能是晚期PACC的一种有效治疗选择。