Middleton Simon B, Clark Susan K, Matravers Paul, Katz David, Reznek Rodney, Phillips Robin K S
The Polyposis Registry, St. Mark's Hospital, Harrow, United Kingdom.
Dis Colon Rectum. 2003 Apr;46(4):481-5. doi: 10.1007/s10350-004-6586-1.
Desmoids are rare, locally aggressive but nonmetastasizing clonal proliferations of fibroblasts that occur both sporadically and in association with familial adenomatous polyposis. Most occur in intra-abdominal sites, where they may lead to major morbidity and mortality. A proposed desmoid precursor lesion occurs in the mesentery of one-third of patients with familial adenomatous polyposis, and postoperative mesenteric fibromatosis has been identified in 20 percent of such patients. True desmoids occur in 10 percent, which suggests a model of development in which the phenotype becomes increasingly severe in a manner analogous to the adenoma-carcinoma sequence. This work aimed to confirm such a progression.
A five-point CT scoring system for mesenteric fibromatosis and desmoids was devised and validated, and in doing so, their incidence was observed. In the second part of the study, seven patients known to have a precursor lesion underwent abdominal CT a median of 27.5 months after the surgery that identified the lesion. Scans were assessed by the scoring system and compared with those of a matched control group of familial adenomatous polyposis patients.
The CT scoring system was reliable and reproducible. Of 103 scans of asymptomatic patients with familial adenomatous polyposis, mesenteric fibromatosis and desmoid tumors were identified in 21 and 2 percent, respectively. In the follow-up of patients with desmoid precursor lesions, those in the precursor lesion group had a significantly greater degree of mesenteric fibromatosis and desmoid formation than their corresponding controls (P = 0.009, Mann-Whitney U test).
A reliable CT scoring system for mesenteric fibromatosis and desmoid tumors in familial adenomatous polyposis is presented. Results with this system provide further evidence for a stepwise progression in the development of desmoids.
韧带样瘤是一种罕见的、局部侵袭性但不发生转移的成纤维细胞克隆性增殖病变,可散发性出现,也可与家族性腺瘤性息肉病相关。大多数发生在腹腔内,可能导致严重的发病率和死亡率。在三分之一的家族性腺瘤性息肉病患者的肠系膜中发现了一种推测的韧带样瘤前体病变,并且在20%的此类患者中发现了术后肠系膜纤维瘤病。真正的韧带样瘤发生在10%的患者中,这提示了一种发展模式,即表型以类似于腺瘤-癌序列的方式变得越来越严重。这项研究旨在证实这种进展。
设计并验证了一种用于肠系膜纤维瘤病和韧带样瘤的五点CT评分系统,并观察了它们的发病率。在研究的第二部分,7名已知有前体病变的患者在确定病变的手术后中位27.5个月接受了腹部CT检查。扫描结果通过评分系统进行评估,并与家族性腺瘤性息肉病患者的匹配对照组进行比较。
CT评分系统可靠且可重复。在103例无症状的家族性腺瘤性息肉病患者的扫描中,分别在21%和2%的患者中发现了肠系膜纤维瘤病和韧带样瘤。在对韧带样瘤前体病变患者的随访中,前体病变组患者的肠系膜纤维瘤病和韧带样瘤形成程度明显高于相应的对照组(曼-惠特尼U检验,P = 0.009)。
提出了一种用于家族性腺瘤性息肉病中肠系膜纤维瘤病和韧带样瘤的可靠CT评分系统。该系统的结果为韧带样瘤发展中的逐步进展提供了进一步的证据。