Lee Joo Hyung, Kim Hyung Sun, Park Ji Hyun, Park Joon Seong
Pancreatobiliary Cancer Clinic, Department of Surgery.
Department of Pathology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Medicine (Baltimore). 2021 Jan 22;100(3):e24310. doi: 10.1097/MD.0000000000024310.
Intraductal papillary mucinous neoplasm of the biliary tract (IPNB) is a rare, low-grade neoplasm limited to the bile duct mucosa. The malignant transformation rate is low, and there have been limited reports of metastasis to other organs. Herein, we presented a rare case of a patient who was diagnosed with IPNB concurrent with invasive adenocarcinoma after surgery and was diagnosed with cardiac metastasis 6 months later.
A 61-year-old male patient presented with abdominal pain to a local clinic. He was diagnosed with intrahepatic cholangiocarcinoma with pancreatitis and transferred to our hospital.
Diagnostic testing (magnetic resonance imaging, endoscopic retrograde cholangiopancreatography, positron emission tomography-computed tomography) revealed a papillary neoplasm and invasive adenocarcinoma with papillary neoplasm in the periampullary lesion.
Pancreaticoduodenectomy, right hemihepatectomy, and left lateral sectionectomy of the liver were performed. After surgery, we planned gemcitabine-based adjuvant chemotherapy.
Upon completion of the sixth gemcitabine chemotherapy cycle, a hyperechoic, oval-shaped mass (1.3 × 2.6 cm) was found on the outer wall of the right atrium. Resection of a cardiac tumor in the right atrium and patch repair were performed.
To our knowledge, no other case of cardiac metastasis found during observation after surgery for an IPNB has been described. IPNBs are known to be less aggressive and to have a lower metastasis rate than intraductal papillary mucinous neoplasms; therefore, the number of case reports describing metastasis after surgery is relatively low. Our case suggests that close observation is necessary in patients diagnosed with an IPNB.
胆管内乳头状黏液性肿瘤(IPNB)是一种罕见的、局限于胆管黏膜的低级别肿瘤。其恶变率较低,转移至其他器官的报道也有限。在此,我们报告一例罕见病例,该患者术后被诊断为IPNB并发浸润性腺癌,6个月后被诊断为心脏转移。
一名61岁男性患者因腹痛到当地诊所就诊。他被诊断为肝内胆管癌合并胰腺炎,随后转至我院。
诊断性检查(磁共振成像、内镜逆行胰胆管造影、正电子发射断层扫描-计算机断层扫描)显示在壶腹周围病变处有乳头状肿瘤和伴有乳头状肿瘤的浸润性腺癌。
实施了胰十二指肠切除术、右半肝切除术和肝左外叶切除术。术后,我们计划进行以吉西他滨为基础的辅助化疗。
在完成第六个吉西他滨化疗周期后,在右心房外壁发现一个高回声椭圆形肿块(1.3×2.6厘米)。进行了右心房心脏肿瘤切除术和补片修补术。
据我们所知,尚未有其他关于IPNB术后观察期间发现心脏转移的病例报道。已知IPNB的侵袭性比导管内乳头状黏液性肿瘤小,转移率也较低;因此,描述术后转移的病例报告数量相对较少。我们的病例表明,对于诊断为IPNB的患者,密切观察是必要的。