Yu Risheng, Wei Jinshe, Li Rongfen, Zhang Shizheng
Department of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China.
Zhonghua Yi Xue Za Zhi. 2002 Apr 25;82(8):541-5.
To assess the diagnostic value of CT to primary hepatic sarcoma.
The CT findings of 12 cases of primary hepatic sarcomas confirmed by operation and pathology, including leimyosarcoma, liposarcoma, and malignant fibrous histocytoma, 2 cases each, and angiosarcoma, carcinosarcoma, cystadenocarcinosarcoma, mesotheliosarcoma, fibrosarcoma, and malignant lymphoma, one case each, were analysed retrospectively.
Only 2 out of the 12 cases of primary hepatic sarcoma were correctly diagnosed by CT before operation. The CT manifestations of primary hepatic sarcoma, against the operational and pathological findings, could be summarized as two types: solid mass type and cystic mass type. Eight cases were of solid mass type, including 2 cases of liposarcoma, and leiomyosarcoma, angiosarcoma, carcinosarcoma, methotheliosarcoma, fibrosarcoma, and malignant lymphoma, one case each. Plain scanning showed homogeneous or inhomogeneous low-density masses; enhanced scanning showed no marked enhancement or inhomogeneous enhancement, ringed peripheral enhancement, or nodular peripheral enhancement. Peripheral enhancement was a CT feature common to angiosarcoma and lymphoma. The characteristic CT manifestation of liposarcoma was an inhomogeneous mass with well-defined border and multiple intermingled septa. Four cases were of cystic mass type, including 2 cases of malignant fibrous histocytoma, and leimyosarcoma with post-operative recurrence and cystadenocarcinosarcoma, one case each, all manifesting a huge single cystic mass: unilocular in the case of leimyosarcoma with post-operative recurrence and multilocular in the other 3 cases. The wall and/or septa of the cyst had an uneven thickness and were markedly enhanced after contrast administration. Clear solid element and wall nodules were seen in the cystic mass of cystadenocarcinosarcoma.
The CT findings of primary hepatic sarcoma are associated with the pathology of tumor. Some pathological patterns of primary hepatic sarcoma, such as liposarcoma and angiosarcoma, have their own characteristic CT manifestations. However, the diagnosis of most primary hepatic sarcoma lacking characteristic CT manifestations must be based on clinical and laboratory examinations and confirmed by pathology.
评估CT对原发性肝肉瘤的诊断价值。
回顾性分析12例经手术及病理证实的原发性肝肉瘤的CT表现,其中平滑肌肉瘤、脂肪肉瘤、恶性纤维组织细胞瘤各2例,血管肉瘤、癌肉瘤、囊腺肉瘤、间皮肉瘤、纤维肉瘤、恶性淋巴瘤各1例。
12例原发性肝肉瘤术前仅2例被CT正确诊断。原发性肝肉瘤的CT表现与手术及病理结果相比,可归纳为两种类型:实性肿块型和囊性肿块型。实性肿块型8例,包括脂肪肉瘤2例,平滑肌肉瘤、血管肉瘤、癌肉瘤、间皮肉瘤、纤维肉瘤、恶性淋巴瘤各1例。平扫显示均匀或不均匀低密度肿块;增强扫描显示无明显强化或不均匀强化、环形周边强化或结节状周边强化。周边强化是血管肉瘤和淋巴瘤的共同CT特征。脂肪肉瘤的特征性CT表现为边界清晰、有多个交错间隔的不均匀肿块。囊性肿块型4例,包括恶性纤维组织细胞瘤2例,术后复发平滑肌肉瘤、囊腺肉瘤各1例,均表现为巨大单房囊性肿块:术后复发平滑肌肉瘤为单房,其他3例为多房。囊肿壁和/或间隔厚度不均匀,增强后明显强化。囊腺肉瘤的囊性肿块内可见清晰的实性成分和壁结节。
原发性肝肉瘤的CT表现与肿瘤病理相关。原发性肝肉瘤的某些病理类型,如脂肪肉瘤和血管肉瘤,有其自身特征性的CT表现。然而,大多数缺乏特征性CT表现的原发性肝肉瘤的诊断必须基于临床和实验室检查,并经病理证实。