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Congenital cystic adenomatoid malformation is a rare but life-threatening lung anomaly.
The final diagnosis of adenomatoid tumor was made (Figure 3).
Stocker JT, Madewell JE, Drake RM: Congenital cystic adenomatoid malformation of the lung.
In high-risk fetuses with congenital diaphragmatic hernia or a large congenital cystic adenomatoid malformation, ex utero intrapartum treatment is used.
Negative staining for lymphatic marker, (D) D2-40, excluding an adenomatoid tumour of the testis.
Congenital cystic adenomatoid malformations (CCAM) are the most commonly diagnosed prenatal lung malformations and account for approximately 30% to 40% of all congenital anomalies.
Respiratory Distress from a Congenital Cystic Adenomatoid Mallformation.
With sonographic advances came perspicuity, offering for the first time a prenatal glimpse of obstructive uropathy, congenital cystic adenomatoid malformations (CCAM), and myelomeningocele lesions.
The most common tumours that arise from the paratesticular tissue are benign neoplasms, such as leiomyoma, lipoma and adenomatoid tumour.
Chondro-osseous respiratory epithelial adenomatoid hamartoma (COREAH) is an extremely rare type of hamartoma.