Bedi D G, John S D, Swischuk L E
Department of Diagnostic Radiology, University of Texas M. D. Anderson Cancer Center, Houston 77030, USA.
J Clin Ultrasound. 1998 Sep;26(7):345-8. doi: 10.1002/(sici)1097-0096(199809)26:7<345::aid-jcu3>3.0.co;2-9.
We describe the variable sonographic appearances of fibromatosis colli, a disease that presents as a mass-like enlargement of the sternocleidomastoid muscle during the first 8 weeks of life.
Sonograms and records of 12 infants who presented with a sternocleidomastoid mass or torticollis before they were 12 weeks old were retrospectively reviewed for sonographic features (presence of a mass, diffuse muscle enlargement, and echogenicity), medical history, and follow-up data.
Sonographically, 6 infants had only a mass in the sternocleidomastoid muscle, 2 had a mass with fusiform muscle enlargement, and 4 had only muscle enlargement. Five masses were hyperechoic, and 1 mass was of mixed echogenicity. The 2 masses associated with muscle enlargement were hypoechoic. Three cases of diffuse muscle enlargement were of mixed echogenicity, and 1 was hypoechoic. Unusual variations included (1) a mass split longitudinally into 2 components and (2) a diffusely enlarged muscle with a striated pattern of mixed echogenicity. Follow-up in 10 patients at 4 months and in 7 patients at 6 months showed clinical improvement.
Fibromatosis colli usually appears sonographically as a hyperechoic mass or diffuse sternocleidomastoid enlargement of mixed echogenicity. Variations in its appearance should not prevent the correct diagnosis as long as the abnormality is intramuscular and adjacent soft tissues are normal.
我们描述了先天性肌纤维瘤病的多种超声表现,该病在出生后8周内表现为胸锁乳突肌的肿块样增大。
回顾性分析12例12周龄前出现胸锁乳突肌肿块或斜颈的婴儿的超声图像及记录,观察超声特征(肿块的存在、肌肉弥漫性增大及回声情况)、病史及随访数据。
超声检查显示,6例婴儿仅胸锁乳突肌有肿块,2例有肿块伴梭形肌肉增大,4例仅有肌肉增大。5个肿块为高回声,1个肿块为混合回声。与肌肉增大相关的2个肿块为低回声。3例肌肉弥漫性增大为混合回声,1例为低回声。不寻常的表现包括:(1)一个肿块纵向分裂为两个部分;(2)肌肉弥漫性增大且呈混合回声的条纹状。10例患者在4个月时及7例患者在6个月时的随访显示临床症状改善。
先天性肌纤维瘤病在超声上通常表现为高回声肿块或胸锁乳突肌弥漫性增大且为混合回声。只要异常位于肌肉内且相邻软组织正常,其表现的变化不应妨碍正确诊断。