Department of Nuclear Medicine, Misgav La-Dach Hospital, Jerusalem, Israel.
Clin Nucl Med. 2013 Mar;38(3):221-2. doi: 10.1097/RLU.0b013e3182814c80.
This is a case of a 4-year-old female child with gross left lower extremity deformity detected at birth, including a giant cutaneous hemangioma from flank to foot. She was found to have no other associated abnormalities and was diagnosed with Klippel-Trénaunay syndrome. This is a rare entity and literature regarding use of radionuclide imaging techniques to evaluate this is scarce. We present here bone and red cell scans performed to evaluate whether there was osseous involvement or only soft tissue disease, which showed classic signs of this condition. Patient photographs also show the syndrome's typical appearance.
这是一例 4 岁女性患儿，出生时即发现左下肢严重畸形，包括从侧腹至足部的巨大皮肤血管瘤。患儿无其他相关异常，被诊断为 Klippel-Trénaunay 综合征。该病较为罕见，有关评估该病的核素成像技术的文献也很少。我们在此报告了进行的骨骼和红细胞扫描，以评估是否存在骨累及或仅软组织疾病，这些扫描显示了该病的典型征象。患者照片也显示了该综合征的典型表现。
