Brooks A P, Reznek R H, Nugent K, Farmer K C, Thomson J P, Phillips R K
Department of Diagnostic Radiology, St Bartholomew's Hospital, London.
Clin Radiol. 1994 Sep;49(9):601-7. doi: 10.1016/s0009-9260(05)81875-6.
Intra-abdominal desmoid tumours represent a major cause of morbidity and mortality in patients with familial adenomatous polyposis (FAP), and such patients are also liable to develop musculoskeletal desmoids. We have reviewed the CT appearances of 44 desmoid lesions (28 intra-abdominal and 16 musculoskeletal) in 20 patients with FAP. We found a considerable heterogeneity in the CT appearance of musculoskeletal and intraabdominal desmoids, with respect to their density, definition and change in size or density on follow-up, not only between different patients but also in patients with multiple lesions, who rarely showed identical appearances of all lesions. In some cases, mesenteric tumours may initially present as ill-defined soft tissue infiltration of mesenteric fat, becoming larger and more mass-like with time. On medical treatment, shrinkage was seen infrequently in musculoskeletal desmoids, and not at all with mesenteric lesions. CT evidence of bowel involvement by intra-abdominal lesions was frequent, most commonly appearing as 'tethering' or encasement of bowel loops. The presence of a large mesenteric mass (> 10 cm diam.), multiple mesenteric masses, extensive small bowel involvement and/or bilateral hydronephrosis were associated with ultimate death.
腹内硬纤维瘤是家族性腺瘤性息肉病(FAP)患者发病和死亡的主要原因,此类患者还容易发生肌肉骨骼系统的硬纤维瘤。我们回顾了20例FAP患者中44个硬纤维瘤病灶(28个腹内病灶和16个肌肉骨骼病灶)的CT表现。我们发现,肌肉骨骼和腹内硬纤维瘤的CT表现存在相当大的异质性,不仅在不同患者之间,而且在有多发病灶的患者中,其密度、边界以及随访时大小或密度的变化方面很少有所有病灶表现均相同的情况。在某些病例中,肠系膜肿瘤最初可能表现为肠系膜脂肪界限不清的软组织浸润,随着时间推移会变得更大且更像肿块。在药物治疗方面,肌肉骨骼硬纤维瘤很少出现缩小,肠系膜病灶则根本没有缩小。腹内病灶累及肠管的CT证据很常见,最常见的表现是肠袢“受牵拉”或被包绕。存在大的肠系膜肿块(直径>10 cm)、多个肠系膜肿块、广泛的小肠受累和/或双侧肾积水与最终死亡相关。