We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.
To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure no-reply@cambridge.org
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
Prenatally diagnosed congenital lung malformations represent a wide variety of fetal pulmonary and airway anomalies, some of which may require close monitoring and perinatal follow-up. Historically these masses were only typically seen when they were very large, at which point they were associated with a high incidence of hydrops and a high termination rate; therefore a diagnosis of a fetal lung mass had a guarded prognosis. Widespread use of prenatal ultrasound improved detection of these masses and advances in surgical techniques have allowed for intervention in the fetal period. More recently, a better understanding of fetal physiology and the use of prenatal steroids has reduced the number of fetuses requiring in-utero intervention. When indicated, in-utero treatment requires a multidisciplinary approach with close attention given to the fetal physiology, risk of maternal complications, and unique anesthetic considerations.
This chapter outlines the prenatal imaging and clinical diagnoses of neonatal and pediatric tumors. It discusses the antenatal natural history, and reviews available treatment options during the pre- and postnatal period for fetuses with prenatally diagnosed tumors. The differential diagnosis of a prenatally diagnosed intracranial tumor includes teratoma, which make up the majority of lesions, hemangioma and papilloma. Prenatal ultrasonography and fetal MRI are useful in evaluating and determining the etiology of the intracranial tumor. The surgical approach to bronchopulmonary sequestrations (BPS) is straightforward, with a muscle sparing thoracotomy or thoracoscopic approach for chest lesions and laparotomy or laparoscopy for subdiaphragmatic BPS, with particular attention to first controlling the anomalous blood supply in all cases. The most common primary hepatic tumor is hemangioma, followed by mesenchymal hamartoma, and hepatoblastoma. The differential diagnosis of mesoblastic nephroma includes hydronephrosis and multicystic dysplastic kidney, focal renal dysplasia, and diffuse nephroblastomatosis and nephroblastoma.
Recommend this
Email your librarian or administrator to recommend adding this to your organisation's collection.