Bura R, Manca Antonio, Ambu R, Pisano G, Melis Alessandro, Maturo A, Erdas E, Nicolosi A, Calò P G
G Chir. 2017 Mar-Apr;38(2):84-89. doi: 10.11138/gchir/2017.38.2.084.
Very few cases of gastric paragangliomas have been reported in the literature to date. We report a rare case of parietal gastric paraganglioma fortuitously detected during intraoperative exploration. A 82-years-old woman presented to our emergency room for abdominal pain. On physical examination abdomen was painful on palpation and Blumberg's sign was present. The laboratory exams showed a neutrophilia in absence of leukocytosis. Acute appendicitis was suspected and a laparoscopy was performed. At exploration, the vermiform appendix was normal while a lumpy, hard-fibrous and white-pinkish extraluminal lesion of the anterior wall of the gastric body near the greater curvature of about 2 cm in diameter was present. Laparoscopic resection of the gastric lesion was performed. The patient was discharged in good condition in the fourth postoperative day. Pathologic examination revealed a gangliocitic paraganglioma. The patient is alive and well without evidence of relapse 6 months after surgery. Gastric paraganglioma is a very rare tumor and its diagnosis is very difficult. Surgical excision is the treatment of choice which can be performed successfully with laparoscopy.
迄今为止,文献中报道的胃副神经节瘤病例非常少。我们报告了一例罕见的胃体部副神经节瘤,在术中探查时偶然发现。一名82岁女性因腹痛就诊于我们的急诊室。体格检查发现腹部触诊疼痛,存在反跳痛。实验室检查显示中性粒细胞增多但无白细胞增多。怀疑为急性阑尾炎,遂行腹腔镜检查。探查时,阑尾正常,而在胃体前壁大弯侧附近有一个直径约2厘米的块状、硬纤维状、白粉色的腔外病变。对胃病变进行了腹腔镜切除。患者术后第四天情况良好出院。病理检查显示为神经节细胞性副神经节瘤。患者术后6个月存活且状况良好,无复发迹象。胃副神经节瘤是一种非常罕见的肿瘤,其诊断非常困难。手术切除是首选治疗方法,腹腔镜手术可成功进行。