Kaminopetros P, Jauniaux E, Kane P, Weston M, Nicolaides K H, Campbell D J
Fetal Medicine Unit, St James's University Hospital, Leeds, UK.
Br J Radiol. 1997 Jul;70(835):750-3. doi: 10.1259/bjr.70.835.9245887.
An unusual case of fetal lymphangioma diagnosed before delivery is reported in a second trimester pregnant woman. The lymphangioma was suspected at 28 weeks on the basis of the ultrasound appearances and progression of the lesions with advancing gestation. MRI was used to evaluate the extent and the tissue characteristics of the lesions. Cytology of the fluid aspirated from the cystic lesions showed abundant lymphocytes and macrophages, confirming the diagnosis of a lymphangioma. The parents opted for a pregnancy termination because of the rapid growth of the lesions and the poor prognosis. It is suggested that the combination of these tests could enable the early diagnosis of these tumours at a stage when the lesion is relatively limited and accessible to therapy in utero.
本文报道了一例孕中期孕妇在分娩前诊断出胎儿淋巴管瘤的罕见病例。根据超声表现及随着孕周增加病变的进展情况,在孕28周时怀疑为淋巴管瘤。采用磁共振成像(MRI)评估病变的范围和组织特征。从囊性病变中抽出的液体进行细胞学检查,显示有大量淋巴细胞和巨噬细胞,确诊为淋巴管瘤。由于病变生长迅速且预后不良,父母选择了终止妊娠。建议这些检查相结合能够在病变相对局限且可在子宫内进行治疗的阶段实现对这些肿瘤的早期诊断。