Pilecki Stanisław, Gierach Marcin, Gierach Joanna, Swiętaszczyk Cyprian, Junik Roman, Lasek Władysław
Laboratory of Nuclear Medicine, Regional Specialist Hospital in Grudziądz, Grudziądz, Poland ; Laboratory of Nuclear Medicine, Department of Endocrinology and Diabetology, Nicolaus Copernicus University in Toruń, Collegium Medicum in Bydgoszcz, Bydgoszcz, Poland.
Laboratory of Nuclear Medicine, Department of Endocrinology and Diabetology, Nicolaus Copernicus University in Toruń, Collegium Medicum in Bydgoszcz, Bydgoszcz, Poland.
Pol J Radiol. 2014 Feb 14;79:27-32. doi: 10.12659/PJR.889874. eCollection 2014.
Congenital vascular malformations are tumour-like, non-neoplastic lesions caused by disorders of vascular tissue morphogenesis. They are characterised by a normal cell replacement cycle throughout all growth phases and do not undergo spontaneous involution. Here we present a scintigraphic image of familial congenital vascular malformations in two sisters.
MATERIAL/METHODS: A 17-years-old young woman with a history of multiple hospitalisations for foci of vascular anomalies appearing progressively in the upper and lower right limbs, chest wall and spleen. A Parkes Weber syndrome was diagnosed based on the clinical picture. Due to the occurrence of new foci of malformations, a whole-body scintigraphic examination was performed. A 12-years-old girl reported a lump in the right lower limb present for approximately 2 years, which was clinically identified as a vascular lesion in the area of calcaneus and talus. Phleboscintigraphy visualized normal radiomarker outflow from the feet via the deep venous system, also observed in the superficial venous system once the tourniquets were released. In static and whole-body examinations vascular malformations were visualised in the area of the medial cuneiform, navicular and talus bones of the left foot, as well as in the projection of right calcaneus and above the right talocrural joint.
People with undiagnosed disorders related to the presence of vascular malformations should undergo periodic follow-up to identify lesions that may be the cause of potentially serious complications and to assess the results of treatment. Presented scintigraphic methods may be used for both diagnosing and monitoring of disease progression.
先天性血管畸形是由血管组织形态发生紊乱引起的肿瘤样非肿瘤性病变。其特征是在所有生长阶段细胞更替周期正常,且不会自发消退。在此,我们展示了两姐妹家族性先天性血管畸形的闪烁显像图像。
材料/方法:一名17岁年轻女性,有多次因上肢和下肢右侧、胸壁及脾脏逐渐出现血管异常病灶而住院的病史。根据临床表现诊断为帕克斯·韦伯综合征。由于出现了新的畸形病灶,进行了全身闪烁显像检查。一名12岁女孩报告右下肢有一肿块,已存在约2年,临床诊断为跟骨和距骨区域的血管病变。静脉闪烁显像显示放射性示踪剂从足部经深静脉系统正常流出,松开止血带后在浅静脉系统也观察到这种情况。在静态和全身检查中,血管畸形在左脚内侧楔骨、舟骨和距骨区域以及右跟骨投影处和右距小腿关节上方显影。
患有与血管畸形相关未确诊疾病的患者应定期随访,以识别可能导致潜在严重并发症的病变,并评估治疗效果。所展示的闪烁显像方法可用于疾病的诊断和进展监测。