1The Polyposis Registry, St Mark's Hospital, Harrow, United Kingdom.
Dis Colon Rectum. 2012 Jul;55(7):810-4. doi: 10.1097/DCR.0b013e318257fa93.
Familial adenomatous polyposis-related desmoid tumors can present with a liquefied center containing gas, accompanied by abdominal pain and sepsis. To date the optimal management of such patients has not been documented.
The aim of this study was to review our experience of managing these desmoids grouped together as "intra-abdominal desmoids with air-fluid level" and present a management algorithm.
This is a retrospective study of prospectively maintained polyposis registry database.
This study was conducted at a tertiary referral center specializing in familial adenomatous polyposis and desmoid disease.
Nine patients with intra-abdominal desmoid and air-fluid level were analyzed for the purpose of this study.
Two hundred and forty-six patients were identified with desmoid tumor. Of these, a total of 9 patients had an intra-abdominal desmoid with air-fluid level; 7 were women. Age range at diagnosis was 20 to 41 years. The median time from primary surgery to desmoid tumor development was 24 months (range, 0-48 months), and the median time for further progression to air-fluid level was 24 months (range, 0-226 months). Desmoid tumor size ranged from 10 cm to greater than 20 cm in diameter. Two patients were successfully managed with antibiotics alone, and 2 patients were managed with percutaneous drainage and antibiotics. The other 5 patients required surgical intervention involving either excision or drainage with or without proximal defunctioning/exclusion. There was a single 30-day mortality.
This study was limited by the small number of patients.
The majority of intra-abdominal desmoids with an air-fluid level require surgical intervention. Antibiotics and percutaneous drainage are only successful in a limited number of patients. We present our current treatment algorithm based on this experience.
家族性腺瘤性息肉病相关的硬纤维瘤可出现液化中心,内含气体,并伴有腹痛和脓毒症。迄今为止,尚未记录此类患者的最佳治疗方法。
本研究旨在回顾我们对这些硬纤维瘤的治疗经验,这些硬纤维瘤被归类为“腹腔内伴有气液平面的硬纤维瘤”,并提出一种治疗方案。
这是一项对前瞻性维护的息肉病登记数据库进行的回顾性研究。
本研究在一家专门从事家族性腺瘤性息肉病和硬纤维瘤病的三级转诊中心进行。
为进行本研究,共分析了 9 例腹腔内伴有气液平面的硬纤维瘤患者。
共确定了 246 例硬纤维瘤患者。其中,共有 9 例患者患有腹腔内伴有气液平面的硬纤维瘤;其中 7 例为女性。诊断时的年龄范围为 20 岁至 41 岁。从初次手术到硬纤维瘤发病的中位时间为 24 个月(范围,0-48 个月),进一步进展为气液平面的中位时间为 24 个月(范围,0-226 个月)。硬纤维瘤大小从 10 厘米到直径大于 20 厘米不等。有 2 例患者仅用抗生素成功治疗,2 例患者采用经皮引流和抗生素治疗。另外 5 例患者需要手术干预,包括切除或引流,伴或不伴近端结肠造口术/旷置术。有 1 例患者发生 30 天死亡。
本研究受到患者数量较少的限制。
大多数腹腔内伴有气液平面的硬纤维瘤需要手术干预。抗生素和经皮引流仅对少数患者有效。我们根据这一经验提出了目前的治疗方案。