Tu Chaoyong, Lin Qiaomei, Zhu Jingde, Shao Chuxiao, Zhang Kun, Jiang Chuan, Ding Zhiyong, Zhou Xingmu, Tu Jiefei, Zhu Wanlin, Chen Wei
Department of General Surgery, Lishui Central Hospital, Lishui, Zhejiang 323000, P.R. China.
Department of Pathology, Lishui Central Hospital, Lishui, Zhejiang 323000, P.R. China.
Exp Ther Med. 2016 Jun;11(6):2379-2384. doi: 10.3892/etm.2016.3221. Epub 2016 Apr 4.
Sarcoidosis is a multisystemic disease of unknown origin characterized by the formation of non-caseating granulomas. Thoracic involvement is the most common presentation; however, sarcoidosis can involve almost any other organ. To the best of our knowledge there have been only 10 cases of splenic sarcoidosis reported in the English literature, with no reports of sarcoidosis of an accessory spleen. The present study reports a case of isolated sarcoidosis of an accessory spleen in the greater omentum, which was identified postoperatively in a 44-year-old female. Chest X-ray results were normal. Gastric endoscopy demonstrated an ulcer in the antrum, which was confirmed to be a signet-ring cell carcinoma via biopsy. Computed tomography of the abdomen revealed mild thickening of the posterior antrum, and a mass in the inferior pole of the left kidney. Intraoperatively, no masses were detected in the liver and spleen. Moreover, no enlarged lymph nodes were detected in the abdominal cavity, pelvic cavity, mesenteric and para-aorta. Following a radical distal gastrectomy and left radical nephrectomy, postoperative pathology demonstrated signet-ring cell carcinoma in the antrum, left renal clear cell cancer and a red lesion measuring 0.5×0.5 cm in the greater omentum, which was similar to the spleen in the splenic cavity and was regarded as an accessory spleen. Following exclusion of fungi and acid-fast bacilli as causative agents, sarcoidosis of the accessory spleen in the greater omentum was confirmed. The patient recovered uneventfully and was discharged on day 8 postoperation. The patient remained alive after two-year follow-up without sarcoidosis and malignant tumor recurrence. The present case demonstrated that, intraoperatively, comprehensive exploration should be conducted to exclude the accessory spleen, which may also suffer from sarcoidosis.
结节病是一种病因不明的多系统疾病,其特征是形成非干酪样肉芽肿。胸部受累是最常见的表现;然而,结节病几乎可累及任何其他器官。据我们所知,英文文献中仅报道了10例脾结节病,尚无副脾结节病的报道。本研究报告了一例大网膜副脾孤立性结节病,该病例是在一名44岁女性患者术后发现的。胸部X线检查结果正常。胃镜检查显示胃窦有溃疡,经活检证实为印戒细胞癌。腹部计算机断层扫描显示胃窦后壁轻度增厚,左肾下极有一肿块。术中,肝脏和脾脏未发现肿块。此外,腹腔、盆腔、肠系膜和腹主动脉旁未发现肿大淋巴结。在进行远端胃癌根治术和左肾根治性切除术后,术后病理显示胃窦印戒细胞癌、左肾透明细胞癌以及大网膜内一个0.5×0.5 cm的红色病变,该病变在脾腔内与脾脏相似,被认为是副脾。在排除真菌和抗酸杆菌作为病原体后,确诊为大网膜副脾结节病。患者恢复顺利,术后第8天出院。经过两年随访,患者存活,无结节病和恶性肿瘤复发。本病例表明,术中应进行全面探查以排除可能患有结节病的副脾。