Kobayashi Masahiro, Matsumura Masaru, Takazawa Yutaka, Shindoh Junichi, Hashimoto Masaji
Gastroenterological Surgery, Toranomon Hospital, Tokyo, JPN.
Pathology, Toranomon Hospital, Tokyo, JPN.
Cureus. 2025 May 18;17(5):e84316. doi: 10.7759/cureus.84316. eCollection 2025 May.
Pleomorphic-type anaplastic carcinoma of the pancreas is a rare and highly aggressive histological subtype of pancreatic ductal carcinoma. It is characterized by rapid progression and a poor prognosis. Preoperative diagnosis is often challenging due to nonspecific imaging findings and the frequent absence of elevated tumor markers. We present a resected case of pleomorphic-type anaplastic carcinoma of the pancreatic tail, which showed early recurrence in the remnant pancreas, potentially associated with a delayed-onset pancreatic fistula. A 63-year-old man presented with upper abdominal pain. Imaging revealed a cystic lesion in the pancreatic tail. Follow-up imaging showed enlargement of the lesion, and a retention cyst with possible underlying pancreatic carcinoma was suspected. Endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) was not performed due to concerns for cyst rupture. The patient underwent distal pancreatectomy with splenectomy. Histopathological examination confirmed pleomorphic-type anaplastic carcinoma. Although the drain was removed on postoperative day (POD) five due to low amylase levels in the drainage tube, a pancreatic fistula developed on POD 14, resulting in an intractable pancreatic fistula requiring persistent drainage. On POD 53, imaging revealed tumor recurrence in the remnant pancreas, along with peritoneal dissemination and right femoral bone metastasis. Retrospective evaluation of CT on POD 14 showed tumor recurrence compressing the main pancreatic duct, which was suspected to be the cause of the fistula. The patient declined further oncological treatment and died on POD 103. This case highlights the diagnostic and therapeutic challenges of pleomorphic-type anaplastic carcinoma of the pancreas. Early postoperative recurrence can lead to pancreatic stump disruption and the development of intractable pancreatic fistula.
多形性未分化癌是胰腺导管癌中一种罕见且侵袭性很强的组织学亚型。其特点是进展迅速,预后较差。由于影像学表现不具特异性且肿瘤标志物常常不升高,术前诊断往往具有挑战性。我们报告一例胰尾多形性未分化癌切除病例,该病例显示残胰早期复发,可能与迟发性胰瘘有关。一名63岁男性因上腹部疼痛就诊。影像学检查发现胰尾有一个囊性病变。后续影像学检查显示病变增大,怀疑是潴留性囊肿伴潜在胰腺癌。因担心囊肿破裂未进行超声内镜引导下细针穿刺活检(EUS-FNA)。患者接受了胰体尾切除术加脾切除术。组织病理学检查确诊为多形性未分化癌。尽管术后第5天因引流管淀粉酶水平低而拔除了引流管,但术后第14天发生了胰瘘,导致形成难治性胰瘘,需要持续引流。术后第53天,影像学检查显示残胰肿瘤复发,伴有腹膜播散和右股骨转移。回顾术后第14天的CT检查发现肿瘤复发压迫主胰管,怀疑这是胰瘘的原因。患者拒绝进一步的肿瘤治疗,于术后第103天死亡。该病例凸显了胰腺多形性未分化癌在诊断和治疗方面的挑战。术后早期复发可导致胰残端破裂和难治性胰瘘的发生。