Thompson William M, Levy Angela D, Aguilera Nadine S, Gorospe Luis, Abbott Robert M
Department of Radiology, Duke University Medical Center, Erwin Road, Box 3808, Durham, NC 27710, USA.
Radiology. 2005 Apr;235(1):106-15. doi: 10.1148/radiol.2351040308. Epub 2005 Mar 4.
To retrospectively review clinical, pathologic, and imaging features of angiosarcoma of the spleen in 12 patients.
Institutional review board approval was obtained, and informed consent was not required. Records of 12 cases of proved angiosarcoma of the spleen were accessed from the files of the Armed Forces Institute of Pathology. Clinical, pathologic, and imaging findings were reviewed. Presenting signs and symptoms were recorded, and the pathologist confirmed the diagnosis and determined gross and microscopic morphologic findings in each spleen. Radiologists reviewed available images to determine the size of the spleen and mass, amount of splenic involvement by the tumor (if enhanced at computed tomography [CT] and magnetic resonance [MR] imaging), and amount of nonviable tumor determined as decreased echogenicity at ultrasonography (US) and lack of enhancement at CT and MR imaging. Imaging and pathologic findings were compared. Five US, 10 CT, three MR, and two angiographic images were reviewed by two experienced abdominal radiologists.
There were seven men and five women (age range, 36-86 years; mean, 55 years). The most common symptom was upper abdominal pain in eight (67%) patients: Pain was acute for 24 hours prior to admission in one patient and chronic (range, 1-6 months) in seven patients. At imaging, the spleen was enlarged (>12 cm in length) in nine patients. The most common finding, seen in seven (58%) patients, was a complex mass or masses in an enlarged spleen. Four of these patients had evidence of metastases and one had intraperitoneal hemorrhage. Two patients had solitary hypervascular tumors and liver metastases. One patient had a normal-sized spleen with multiple lesions that ranged 2-3 cm in size, as well as metastases to the spine. The 11th patient had two small lesions, with small calcifications in the periphery of one lesion. The 12th patient had intraabdominal hemorrhage around the spleen and no obvious mass at CT. Tumor necrosis was confirmed at histologic evaluation in nine patients.
The most common clinical finding was upper abdominal pain. Angiosarcoma of the spleen could be suggested in the majority of cases (83%) by using the imaging features of splenic mass with evidence of metastatic disease.
回顾性分析12例脾血管肉瘤患者的临床、病理及影像学特征。
本研究获得机构审查委员会批准,无需患者知情同意。从武装部队病理研究所的档案中获取12例经证实的脾血管肉瘤病例记录。对临床、病理及影像学检查结果进行回顾。记录患者的症状和体征,病理学家确认诊断并确定每个脾脏的大体和显微镜下形态学特征。放射科医生查看现有影像资料,以确定脾脏和肿块的大小、肿瘤累及脾脏的范围(计算机断层扫描[CT]和磁共振成像[MR]增强扫描表现)以及超声检查(US)显示的无活性肿瘤范围(表现为回声减低)和CT及MR成像显示的无强化范围。对比影像学和病理检查结果。两位经验丰富的腹部放射科医生查看了5例超声、10例CT、3例MR及2例血管造影图像。
患者共7例男性和5例女性(年龄范围36 - 86岁;平均55岁)。最常见的症状是8例(67%)患者出现上腹部疼痛:1例患者入院前24小时为急性疼痛,7例患者为慢性疼痛(持续时间1 - 6个月)。影像学检查显示,9例患者脾脏增大(长度>12 cm)。最常见的表现为7例(58%)患者脾脏增大并伴有复杂肿块。其中4例患者有转移证据,1例患者有腹腔内出血。2例患者有孤立性富血管肿瘤及肝转移。1例患者脾脏大小正常,有多个大小为2 - 3 cm的病灶,并有脊柱转移。第11例患者有2个小病灶,其中1个病灶周边有小钙化灶。第12例患者脾脏周围有腹腔内出血,CT检查未见明显肿块。9例患者经组织学评估证实有肿瘤坏死。
最常见的临床症状是上腹部疼痛。大多数病例(83%)可根据脾脏肿块伴有转移证据的影像学特征提示脾血管肉瘤。