Fan XiaoYu, Wang WenYue, Li ChaoFeng, Tang Tao, Han YongXin, An Ke
Peking University China-Japan Friendship School of Clinical Medicine.
Department of General Surgery, China-Japan Friendship Hospital, Beijing, China.
Medicine (Baltimore). 2019 Apr;98(16):e15246. doi: 10.1097/MD.0000000000015246.
Mucinous cystic neoplasms (MCNs) are relatively rare lesions, accounting for 2%-5% of all exocrine pancreatic neoplasms. MCNs mainly occur in women (female:male ratio = 20:1), with a peak incidence in the 5th decade of life. Osteoclast-like giant cell tumors (OGCTs) are rare and relatively aggressive neoplasms, comprising <1% of all pancreatic carcinomas. Herein, we present a rare "combination tumor" case and discuss the impact of mural nodules in pancreatic MCNs considering malignant transformation.
A 54-year-old Mongolian man, without vomiting, nausea or jaundice, presented with abdominal distention since 3 months. He had a 7-year history of diabetes. Physical examinations indicated slight middle abdominal tenderness without rebound tenderness or rigidity. Laboratory results revealed that the level of carcinoembryonic antigen (CEA) was 1.16 ng/ml (normal: <5 ng/ml); CA-199: 30.02 U/ml (normal: <27 U/ml); hemoglobin: 143 g/L; fasting glucose: 7.71 mmol/L; and albumin: 43 g/L. Abdominal enhanced computed tomography revealed a 7 × 6 cm solid neoplasm in the pancreatic body with partial enhancement and heterogeneity. Endoscopic ultrasound revealed a solid-cystic space-occupying lesion in the pancreatic body.
The preoperative preliminary diagnosis was pancreatic solid-cystic tumor, possibly a solid pseudopapillary tumor. Postoperative pathological findings revealed a pancreatic borderline MCN with an OGCT embedded in a mural nodule of the capsule. Immunohistochemical results indicated a simultaneous dual origin from the epithelium and stroma.
The patient underwent open distal pancreatectomy and splenectomy. Postoperative blood glucose levels were closely monitored and regulated. We intravenously administered single-agent gemcitabine (1400 mg on day 1) as the first-time chemotherapy, 1 month after surgery. After the first chemotherapy, the patient refused to receive further treatment owing to personal reasons.
The patient showed uneventful recovery and was discharged 13 days after the initial surgery. Follow-up was performed 1, 3 and 6 months after surgery. At 6 months, abdominal computed tomography scan showed no signs of recurrence, regional lymphadenopathy, or other abnormalities. And laboratory tests showed a platelet count of 301 × 10/L, postprandial blood glucose of 12.9 mmol/L and CA-199 level of 20 U/ml. The patient had no obvious discomfort.
Although pancreatic MCNs are widely accepted as borderline tumors, malignant transformations may occur due to various risk factors (cyst size, mural nodules, septations, and tumor location). The combination tumor in this case was more likely to increase the possibility of malignant biological behavior, thereby worsening overall prognosis. Therefore, long-term follow-up must be maintained with strict monitoring.
黏液性囊性肿瘤(MCNs)是相对罕见的病变,占所有胰腺外分泌肿瘤的2% - 5%。MCNs主要发生于女性(男女比例为20:1),发病高峰在50岁左右。破骨细胞样巨细胞瘤(OGCTs)罕见且具有相对侵袭性,占所有胰腺癌的比例不到1%。在此,我们报告一例罕见的“复合型肿瘤”病例,并讨论胰腺MCNs中壁结节对恶性转化的影响。
一名54岁的蒙古族男性,无呕吐、恶心或黄疸症状,3个月来一直腹胀。他有7年糖尿病史。体格检查显示中上腹轻度压痛,无反跳痛或肌紧张。实验室检查结果显示,癌胚抗原(CEA)水平为1.16 ng/ml(正常:<5 ng/ml);CA - 199:30.02 U/ml(正常:<27 U/ml);血红蛋白:143 g/L;空腹血糖:7.71 mmol/L;白蛋白:43 g/L。腹部增强计算机断层扫描显示胰体部有一个7×6 cm的实性肿瘤,部分强化且不均匀。内镜超声显示胰体部有一个实性 - 囊性占位性病变。
术前初步诊断为胰腺实性 - 囊性肿瘤,可能为实性假乳头状瘤。术后病理结果显示为胰腺交界性MCN,在包膜壁结节中嵌有OGCT。免疫组化结果表明其同时起源于上皮和间质。
患者接受了开放性远端胰腺切除术和脾切除术。术后密切监测和调节血糖水平。术后1个月,我们静脉注射单药吉西他滨(第1天1400 mg)作为首次化疗。首次化疗后,患者因个人原因拒绝接受进一步治疗。
患者恢复顺利,初次手术后13天出院。术后1、3和6个月进行了随访。6个月时,腹部计算机断层扫描显示无复发迹象、区域淋巴结肿大或其他异常。实验室检查显示血小板计数为301×10/L,餐后血糖为12.9 mmol/L,CA - 199水平为20 U/ml。患者无明显不适。
尽管胰腺MCNs被广泛认为是交界性肿瘤,但由于各种危险因素(囊肿大小、壁结节、分隔和肿瘤位置)可能会发生恶性转化。本例中的复合型肿瘤更有可能增加恶性生物学行为的可能性,从而恶化总体预后。因此,必须进行长期随访并严格监测。