CHẨN ĐOÁN HÌNH ẢNH TỒN TẠI VÀ QUÁ PHÁT THỂ KÍNH NGUYÊN THỦY (TTTKNT)

Abstract

Objective: To present three rare cases of PHPV in baby which were diagnosed with USG and CT scanner at 2 different syndromes. The authors want to find out the diagnostic imaging capability of this affection on each syndrome.
Material and methode: Cross-section description study of 3 cases with USG and CT scanner.
Result: The patient parent discover when the baby always rubs the eyes because they can’t see anything. Other
clinical examination, the diagnosis is set with UGS as a solid mass in the vitreous corpus, no adherence in the macula,
no hypervascularization on color Doppler image some small calcified nodes at all 2 eyes leading to total blindness.
One of two patient has associated anomalies of the brain: turricephaly, corpus callosum atrophy, lissenpachygyria
calling Aicardi syndrome. CT scanner is indicated only to set the differential diagnosis of retinoblastoma with
calcification and possible extension in the retrobulbar space and optic nerv.
Conclusion: PHPV is a rare anomaly, difficult to prenatale diagnose but easy post delivery by USG, needing
probe over 10 MHz and color doppler; transcranial sonogaphy gives avaluable image. CT is indicated only to detecte
calcification for rule out retinoblastoma. IRM is not necessary except intend to investigate brain malformation.