Vanhoenacker F M, Schepper A M, Raeve H, Berneman Z
Department of Radiology, University Hospital Antwerp, Wilrijkstraat 10, 2650 Edegem, Belgium.
Eur Radiol. 2003 Dec;13 Suppl 4:L35-9.
Cystic angiomatosis is a rare disorder with a poor prognosis. We describe a case of a 33-year-old woman who presented with long-standing bone pain, hemolytic anemia, and an enlarged spleen. Radiologically, multiple osseous lesions with a mixed pattern of lytic and sclerotic areas were seen within the shoulders, spine, and pelvis. On CT and MRI of the abdomen, the spleen was markedly enlarged, with internal hyperdense foci on non-contrast CT scan, corresponding to low signal intensity areas on all MR pulse sequences. After administration of contrast, a mottled enhancement pattern throughout the entire spleen was seen both on CT and MRI. Cystic angiomatosis was proven by histological analysis of a biopsy specimen of an involved vertebra and histopathological examination of the spleen after subsequent splenectomy. This is the first report of a patient with disseminated cystic angiomatosis with splenic involvement in which the MRI features differ from the previous reports. Instead of the usual pattern consisting of multiple well-defined cystic lesions, a diffuse involvement replacing the entire spleen, with heterogeneous signal intensities on T2-weighted images and heterogeneous enhancement pattern, was seen in our patient.
囊性血管瘤病是一种预后较差的罕见疾病。我们描述了一例33岁女性患者,她长期存在骨痛、溶血性贫血和脾脏肿大。放射学检查显示,在肩部、脊柱和骨盆内可见多个溶骨性和硬化性区域混合的骨病变。腹部CT和MRI检查显示,脾脏明显肿大,非增强CT扫描显示内部高密度灶,在所有MR脉冲序列上对应低信号强度区域。注射造影剂后,CT和MRI均显示整个脾脏呈斑驳状强化。通过对受累椎体活检标本的组织学分析以及随后脾切除术后脾脏的组织病理学检查,证实为囊性血管瘤病。这是首例关于弥漫性囊性血管瘤病累及脾脏的患者报告,其MRI特征与以往报告不同。我们的患者未出现通常由多个边界清晰的囊性病变组成的模式,而是整个脾脏弥漫受累,T2加权图像上信号强度不均匀,强化模式也不均匀。