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巨大侵袭性腹腔内硬纤维瘤型纤维组织细胞瘤——病例报告。

Giant aggressive intra-abdominal desmoid-type fibromatosis - case report.

出版信息

Rozhl Chir. 2022 Summer;101(7):337-341. doi: 10.33699/PIS.2022.101.7.337-341.

Abstract

INTRODUCTION

Aggressive fibromatosis, also known as desmoid tumour (DT), is a locally invasive soft tissue malignancy originating from fascial planes, connective tissue, and musculoaponeurotic structures of the muscles. The symptoms greatly depend on the location and size of the tumour.

CASE REPORT

A 68-year-old male patient without any comorbidities with a large, palpable mass in the abdomen underwent computed tomography (CT) of the abdomen during diagnostic examination in September 2017 in another centre. The CT scan revealed a giant intraperitoneal 30×40cm tumour without signs of infiltrating the surrounding organs and large vessels. The tumour biopsy revealed an aggressive DT. The patient was scheduled for tumour resection. Midline laparotomy was performed in the supine position under general anaesthesia. After gaining access to the abdominal cavity, 8 litres of clear ascites were evacuated. The tumour was not attached to the abdominal wall. Large omentum was freed from the DT. The perioperative finding confirmed the CT images of DT encapsulation of the medial colic artery, part of the small intestine, and transverse colon. The tumour was resected with part of the mesenteric radix, 30 cm of small intestine, and 2/3 of the transverse colon. After the DT was removed entirely, the small intestine was re-anastomosed end to end. The abdominal cavity and the liver were carefully checked for bleeding. The abdominal cavity was closed in a standard manner.

RESULTS

The postoperative hospital stay was uneventful. The patient was discharged on the 7th postoperative day with prophylactic low weight molecular heparin for one month. Currently, we have five months of follow-up with no signs of DT recurrence based on CT examination. The histology of the resected tumour confirmed the diagnosis of a desmoid tumour (aggressive abdominal fibromatosis).

CONCLUSION

Desmoid tumours are benign neoplasms with no metastatic potential. However, their treatment is challenging due to their aggressive growth, infiltrative behaviour, and a high tendency to recur.

摘要

简介

侵袭性纤维瘤病,又称韧带样纤维瘤(desmoid tumour,DT),是一种起源于筋膜平面、结缔组织和肌肉的肌筋膜结构的局部侵袭性软组织恶性肿瘤。其症状很大程度上取决于肿瘤的位置和大小。

病例报告

一名 68 岁男性患者,无任何合并症,腹部可触及一个大肿块。2017 年 9 月,在另一中心进行诊断性检查时,进行了腹部计算机断层扫描(CT)。CT 扫描显示巨大的腹膜内 30×40cm 肿瘤,无侵犯周围器官和大血管的迹象。肿瘤活检显示侵袭性 DT。患者计划进行肿瘤切除。全身麻醉下取仰卧位行正中剖腹术。进入腹腔后,排出 8 升清亮腹水。肿瘤未附着于腹壁。大网膜从 DT 中游离出来。围手术期发现证实了 CT 图像上 DT 包裹了结肠内侧动脉、部分小肠和横结肠。肿瘤连同部分肠系膜根部、30cm 小肠和 2/3 横结肠被切除。DT 完全切除后,小肠行端端吻合。仔细检查腹腔和肝脏有无出血。标准关闭腹腔。

结果

术后住院期间无并发症。患者术后第 7 天出院,预防性给予低分子量肝素 1 个月。目前,根据 CT 检查,我们已经随访了 5 个月,没有 DT 复发的迹象。切除肿瘤的组织学证实了韧带样纤维瘤(侵袭性腹部纤维瘤病)的诊断。

结论

韧带样纤维瘤是一种良性肿瘤,无转移潜能。然而,由于其侵袭性生长、浸润性行为和高复发倾向,其治疗具有挑战性。

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