Xu Shao-Yan, Zhou Bo, Wei Shu-Mei, Zhao Ya-Nan, Yan Sheng
Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310000, Zhejiang Province, China.
Department of Pathology, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310000, Zhejiang Province, China.
World J Gastrointest Oncol. 2022 May 15;14(5):1057-1064. doi: 10.4251/wjgo.v14.i5.1057.
Pancreatic accessory spleen (PAS) is an uncommon congenital abnormality of the spleen. Spleen hamartoma (SH) is also rare. Moreover, hamartoma in the PAS has not been reported thus far. We report the first case here.
A 26-year-old male presented with a one-month history of left upper quadrant abdominal pain, and computerized tomography (CT) examination suggested a mass in the pancreas tail. The patient then attended our hospital for diagnosis and treatment. Ultrasonography, CT, and magnetic resonance imaging revealed a solid mass with cystic degeneration growing from the tail of the pancreas. The tumor marker carbohydrate antigen 19-9 (CA19-9) increased to 96.7 U/mL (normal range 0-37 U/mL). An epidermoid cyst in a PAS was considered preoperatively. However, a malignant tumor cannot be ruled out. We performed laparoscopic surgery, and two pancreatic masses were found growing from the pancreatic tail. The two masses were so closely connected that preoperative imaging examinations suggested only one mass. We carefully isolated the masses from the splenic artery and vein. A laparoscopic spleen-preserving distal pancreatectomy was successfully performed. On pathological examination, the masses were well-defined, homogeneous red-tan, 4 × 3, and 4.5 × 1.5 in size, respectively. One of them was cystically degenerated. On microscopical examination, the mass contained unorganized small slit-like vascular channels enclosing red blood cells and lined with plump endothelial cells. No area of cytologic atypia was identified. Focal lymphoid aggregates were found in the intravascular areas. White pulp or fibrosis was not observed. The final diagnosis was pancreatic accessory SH with cystic degeneration. After the operation, CA19-9 was reduced to normal. The patient recovered well, and the 34-mo follow-up period was uneventful.
Here, we report the first case of pancreatic accessory SH. A laparoscopic spleen-preserving distal pancreatectomy was successfully performed. The patient recovered well and had a good prognosis.
胰腺副脾(PAS)是一种罕见的脾脏先天性异常。脾错构瘤(SH)也很罕见。此外,迄今为止尚未有胰腺副脾内错构瘤的报道。我们在此报告首例病例。
一名26岁男性,有左上腹疼痛1个月的病史,计算机断层扫描(CT)检查提示胰尾有一肿块。该患者随后到我院进行诊断和治疗。超声、CT和磁共振成像显示胰尾有一伴有囊性变的实性肿块。肿瘤标志物糖类抗原19-9(CA19-9)升高至96.7 U/mL(正常范围0-37 U/mL)。术前考虑为胰腺副脾内的表皮样囊肿。然而,不能排除恶性肿瘤。我们进行了腹腔镜手术,发现两个胰肿块从胰尾长出。这两个肿块连接紧密,术前影像学检查仅提示一个肿块。我们小心地将肿块与脾动静脉分离。成功实施了腹腔镜保脾远端胰腺切除术。病理检查显示,肿块边界清晰,呈均匀的红棕色,大小分别为4×3和4.5×1.5。其中一个有囊性变。显微镜检查显示,肿块内有杂乱无章的小裂隙样血管通道,包绕着红细胞,内衬丰满的内皮细胞。未发现细胞异型性区域。血管内区域发现局灶性淋巴样聚集。未观察到白髓或纤维化。最终诊断为胰腺副脾错构瘤伴囊性变。术后CA19-9降至正常。患者恢复良好,34个月的随访期无异常。
我们在此报告首例胰腺副脾错构瘤病例。成功实施了腹腔镜保脾远端胰腺切除术。患者恢复良好,预后良好。