Radhakrishnan Rupa, Calvo-Garcia Maria A, Lim Foong-Yen, Elluru Ravindhra G, Koch Bernadette L
Department of Radiology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave., Cincinnati, OH, 45040, USA,
Pediatr Radiol. 2015 Mar;45(3):453-6. doi: 10.1007/s00247-014-3113-y. Epub 2014 Aug 23.
We present a case of an infant with congenital salivary gland anlage tumor, with fetal and postnatal imaging. To the best of our knowledge, this is the first case describing the in utero imaging findings of salivary gland anlage tumor. A fetal MRI was performed secondary to the clinical finding of polyhydramnios, which identified a nasopharyngeal mass. Because findings were concerning for airway obstruction, the fetus was delivered by ex utero intrapartum treatment (EXIT) to airway procedure. A postnatal CT confirmed the findings of the fetal MRI. The lesion was resected when the baby was 4 days old and recovery was uneventful.
我们报告一例患有先天性涎腺始基肿瘤的婴儿病例，并展示了其胎儿期和出生后的影像学表现。据我们所知，这是首例描述涎腺始基肿瘤宫内影像学表现的病例。因临床发现羊水过多，遂对胎儿进行了磁共振成像（MRI）检查，发现鼻咽部有一肿块。鉴于检查结果提示可能存在气道梗阻，遂通过产时宫外治疗（EXIT）气道手术分娩胎儿。出生后的计算机断层扫描（CT）证实了胎儿MRI的检查结果。婴儿4天大时切除了病变，术后恢复顺利。
