Soon David Sc, Shilton Hamish, Andrabi Ali
Department of Surgery, Peninsula Health, Frankston, Victoria, Australia
Department of Surgery, Peninsula Health, Frankston, Victoria, Australia.
J Surg Case Rep. 2016 Dec 18;2016(12):rjw213. doi: 10.1093/jscr/rjw213.
Mesothelial inclusion cyst is a rare benign tumour that has only 130 cases reported in the literature. Accurate diagnosis and optimal management of this condition remains uncertain. We report a 51-year-old African gentleman, whom presents with abdominal pain and constipation. A computed tomography scan was performed and revealed a large cystic lesion in the right paracolic gutter. The differential diagnosis included appendiceal mucinous neoplasm, cystic tuberculosis and duplication cyst. A laparotomy was performed due to his symptoms and size of the cyst. Macroscopically, the tumour had a size of 25 × 10 × 10 cm and revealed a necrotic lymph node. It was resected en bloc with the appendix and an ileocolic anastomosis performed. Histology revealed a diagnosis of mesothelial inclusion cyst and acute appendicitis. The patient recovered well and had no recurrence at 2-year follow-up.
间皮包涵体囊肿是一种罕见的良性肿瘤,文献中仅报道过130例。对此病症的准确诊断和最佳治疗方案仍不明确。我们报告一名51岁的非洲男性,他因腹痛和便秘前来就诊。进行了计算机断层扫描,结果显示右结肠旁沟有一个大的囊性病变。鉴别诊断包括阑尾黏液性肿瘤、囊性结核和重复囊肿。由于他的症状和囊肿大小,进行了剖腹手术。肉眼可见,肿瘤大小为25×10×10厘米,并有一个坏死淋巴结。它与阑尾一并整块切除,并进行了回结肠吻合术。组织学检查显示诊断为间皮包涵体囊肿和急性阑尾炎。患者恢复良好,在2年随访中无复发。