期刊论文详细信息
BMC Medical Imaging
Microbubbles in macrocysts – Contrast-enhanced ultrasound assisted sclerosant therapy of a congenital macrocystic lymphangioma: a case report
Case Report
Carlos Menendez-Castro1  Jörg Jüngert1  Heiko von Goessel1  Fabian Fahlbusch1  Maren Zapke1  Wolfgang Rascher1 
[1] Department of Pediatrics and Adolescent Medicine, University Hospital of Erlangen, Loschgestrasse 15, D-91054, Erlangen, Germany;
关键词: Contrast agent-enhanced ultrasound;    CEUS;    Congenital cystic lymphangioma;    SonoVue®;    Sclerosant therapy;    OK-432;    Picibanil;   
DOI  :  10.1186/s12880-017-0213-9
 received in 2016-11-25, accepted in 2017-07-03,  发布年份 2017
来源: Springer
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【 摘 要 】

BackgroundCongenital cystic lymphangiomas are benign malformations due to a developmental disorder of lymphatic vessels. Besides surgical excision, sclerosant therapy of these lesions by intracavitary injection of OK-432 (Picibanil®), a lyophilized mixture of group A Streptococcus pyogenes, is a common therapeutical option. For an appropriate application of OK-432, a detailed knowledge about the structure and composition of the congenital cystic lymphangioma is essential. SonoVue® is a commercially available contrast agent commonly used in sonography by intravenous and intracavitary application.Case presentationHere we report the case of 2 month old male patient with a large thoracic congenital cystic lymphangioma. Preinterventional imaging of the malformation was performed by contrast-enhanced ultrasound after intracavitary application of SonoVue® immediately followed by a successful sclerotherapy with OK-432.ConclusionsContrast agent-enhanced ultrasound imaging offers a valuable option to preinterventionally clarify the anatomic specifications of a congenital cystic lymphangioma in more detail than by single conventional sonography. By the exact knowledge about the composition and especially about the intercystic communications of the lymphangioma sclerosant therapy becomes safer and more efficient.

【 授权许可】

CC BY   
© The Author(s). 2017

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