Department of Radiology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, Zhejiang Province, China.
World J Gastroenterol. 2013 Jun 14;19(22):3520-3. doi: 10.3748/wjg.v19.i22.3520.
We report a case of pancreatic hemolymphangioma. Hemolymphangioma is a malformation of both lymphatic vessels and blood vessels. The incidence of this disease in the pancreas is extremely rare. To the best of our knowledge, only seven cases have been reported worldwide (PubMed). A 39-year-old woman with a one-day history of abdominal pain was admitted to our hospital. There was no obvious precipitating factor. The preoperative examination, including ultrasonography and computed tomography, showed a cystic-solid tumor in the pancreas, and it was considered to be a mucinous cystadenoma or cystadenocarcinoma. Pancreatic body-tail resection combined with splenectomy was performed. After the operation, the tumor was pathologically demonstrated to be a pancreatic hemolymphangioma. Although pancreatic hemolymphangioma is rare, we believe that it should be considered in the differential diagnosis of cystic-solid tumors of the pancreas, particularly when there is no sufficient evidence for diagnosing cystadenoma, cystadenocarcinoma or some other relatively common disease of the pancreas.
我们报告一例胰腺血淋巴管瘤病例。血淋巴管瘤是淋巴管和血管的畸形。这种疾病在胰腺中的发病率极罕见。据我们所知,全世界仅有 7 例报告(PubMed)。一位 39 岁女性,腹痛 1 天,无明显诱发因素。术前检查,包括超声和 CT,显示胰腺内囊实性肿瘤,考虑为黏液性囊腺瘤或囊腺癌。行胰体尾切除术联合脾切除术。术后病理证实为胰腺血淋巴管瘤。虽然胰腺血淋巴管瘤罕见,但我们认为在胰腺囊实性肿瘤的鉴别诊断中应考虑到该疾病,尤其是在诊断为囊腺瘤、囊腺癌或其他一些相对常见的胰腺疾病的证据不足时。