Paladini D, Vassallo M, Sglavo G, Lapadula C, Longo M, Nappi C
Fetal Cardiology Unit, Department of Gynecology and Obstetrics, University Federico II of Naples, Naples, Italy.
Ultrasound Obstet Gynecol. 2005 Sep;26(3):300-2. doi: 10.1002/uog.1972.
Cavernous lymphangiomas are characterized by penetration through the subcutaneous areas between the muscular septa and represent rare variants of the more common superficial lymphangioma. Although frequently described in the fetus when involving the posterior aspect of the neck (i.e. cystic hygroma), involvement of the craniofacial region is rare. We describe the prenatal findings in a case of cavernous lymphangioma of the fetal face and neck, which extended caudally to envelop the larynx and the trachea. The anomaly was assessed by two- and three-dimensional (3D) ultrasound. The latter approach was used thoroughly both during counseling with the couple and during consultation with the pediatric surgeon. This case report confirms the usefulness of the 3D approach in the management of rare fetal anomalies. In particular, the possibility of navigating the volume facilitated consultation with the pediatric surgeon and counseling of the parents.
海绵状淋巴管瘤的特征是穿透肌间隔之间的皮下区域,是较常见的浅表淋巴管瘤的罕见变体。虽然在胎儿颈部后侧受累时(即囊状水瘤)常被描述,但头面部区域受累罕见。我们描述了一例胎儿面部和颈部海绵状淋巴管瘤的产前检查结果,该淋巴管瘤向尾侧延伸,包绕喉和气管。通过二维和三维(3D)超声对该异常进行评估。在与这对夫妇咨询以及与小儿外科医生会诊期间,都充分使用了后一种方法。本病例报告证实了3D方法在处理罕见胎儿异常中的有用性。特别是,通过对容积进行导航,便于与小儿外科医生会诊以及向父母提供咨询。