Anteby Roi, Sullivan Brianne J, Mani Malary, Golas Benjamin
Division of Surgical Oncology, Mount Sinai Hospital, New York, NY, USA
Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
BMJ Case Rep. 2020 Feb 10;13(2):e232861. doi: 10.1136/bcr-2019-232861.
Inflammatory myofibroblast tumour (IMT) is an uncommon soft tissue tumour with an unpredictable clinical course: mostly benign, occasionally locally aggressive and rarely capable of metastasis. Diagnosed mainly in the mesentery, omentum, retroperitoneum, pelvis and lungs, IMT is extremely rare as a primary gallbladder tumour. Despite improved radiographical capabilities, differentiating the tumour from other more common causes of gallbladder neoplasms necessitates histopathological and immunohistochemistry tests. Once diagnosed, malignant potential should be taken into consideration, striving for an en bloc R0 resection and postoperative long-term follow-up with routine ancillary imaging. The authors present the case of a recurrent primary IMT of the gallbladder, after two surgical treatments, including a pancreaticoduodenectomy. Now 3 years after initial diagnoses the patient is asymptomatic, but has developed local and distant metastases and is being treated with systemic corticosteroid.
炎性肌成纤维细胞瘤(IMT)是一种罕见的软组织肿瘤,临床病程不可预测:大多为良性,偶尔具有局部侵袭性,很少发生转移。IMT主要诊断于肠系膜、大网膜、腹膜后、骨盆和肺部,作为原发性胆囊肿瘤极为罕见。尽管放射影像学能力有所提高,但要将该肿瘤与其他更常见的胆囊肿瘤病因区分开来,仍需要进行组织病理学和免疫组织化学检查。一旦确诊,应考虑其恶性潜能,争取整块R0切除,并在术后进行常规辅助影像学长期随访。作者报告了一例胆囊原发性IMT复发的病例,该患者接受了包括胰十二指肠切除术在内的两次手术治疗。自初次诊断至今已过去3年,患者无症状,但已出现局部和远处转移,目前正在接受全身性皮质类固醇治疗。