Prenatal sonographic diagnosis of an extensive fetal axillary hemangiolymphangioma

Hemangiolymphangioma (HL) is an extremely rare malformation of both the lymphatic and blood vessels. We present a case of fetal axillary HL that was diagnosed sonographically at 36 weeks' gestation. Sonographic examination revealed a large, multilocular, cystic mass consistent with lymphangioma. At birth, a giant hemangioma was noticed involving the right hemitruncus. Based on clinical and sonographic findings, a diagnosis of HL was made. Surgical treatment was considered but was refused by the parents. The neonate died at 14 days of age, possibly due to an intralesional hemorrhage. © 2007 Wiley Periodicals, Inc. J Clin Ultrasound, 2007

[1]  M. Kilby,et al.  The use of high resolution magnetic resonance imaging in the prenatal diagnosis of fetal nuchal tumors , 2005, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[2]  C. Nappi,et al.  Cavernous lymphangioma of the face and neck: prenatal diagnosis by three‐dimensional ultrasound , 2005, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[3]  G. Chavhan,et al.  Sonographic appearance of a congenital parotid gland hemangiolymphangioma simulating malignancy in an infant , 2003, Journal of clinical ultrasound : JCU.

[4]  J. Tseng,et al.  Fetal axillary hemangiolymphangioma with secondary intralesional bleeding: serial ultrasound findings , 2002, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[5]  U. Hanaoka,et al.  Antenatal ultrasonographic features of fetal giant hemangiolymphangioma , 2001, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[6]  S. LaRusso,et al.  Prenatal sonographic diagnosis of axillary cystic lymphangiomas , 2001, Journal of clinical ultrasound : JCU.

[7]  L. Gonçalves,et al.  Klippel–Trenaunay–Weber syndrome presenting as massive lymphangiohemangioma of the thigh: prenatal diagnosis , 2000, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

[8]  S. Jan,et al.  Progressive fetal axillary cystic lymphangioma with coexistent naevus flammeus , 1997, The British journal of dermatology.

[9]  J. Mulliken,et al.  Hemangiomas and vascular malformations of infancy and childhood. , 1993, Pediatric clinics of North America.

[10]  P. Giacalone,et al.  Fetal hemangiolymphangioma: a case report. , 1993, Fetal diagnosis and therapy.

[11]  R. L. Thomas Prenatal diagnosis of giant cystic hygroma: Prognosis, counselling, and management; case presentation and review of the recent literature , 1992, Prenatal diagnosis.

[12]  D. Mitra,et al.  Hemangiolymphangioma of the urinary bladder in a child. , 1987, Journal of pediatric surgery.

[13]  R. Berkowitz,et al.  Fetal Giant Hemangiolymphangioma: Report of a Case , 1987, American journal of perinatology.

[14]  J. Glowacki,et al.  Hemangiomas and Vascular Malformations in Infants and Children: A Classification Based on Endothelial Characteristics , 1982, Plastic and reconstructive surgery.