نتایج جستجو برای: congenital cystic adenomatoid malformation of the lung
تعداد نتایج: 22854740 فیلتر نتایج به سال:
There are several congenital lung lesions that result in severe pulmonary hypoplasia and neonatal death. These malformations include congenital diaphragmatic hernia (CDH), oligohydramnios induced pulmonary hypoplasia, and congenital cystic adenomatoid malformation of the lung. Severely affected newborns are not salvageable by current surgical techniques or medical treatment, although one new ex...
P14.08: First trimester prenatal diagnosis of congenital cystic adenomatoid malformation of the lung
There are many methods for achieving one-lung ventilation (OLV) during thoracic surgery in neonates and the accuracy of OLV may affect postoperative outcome. The authors have performed OLV using a 5 Fr Arndt endobronchial blocker (AEB, Cook Inc., Bloomington, IN, USA) on a neonate diagnosed with congenital cystic adenomatoid malformation and respiratory distress syndrome (RDS) associated with m...
The adenomatoid tumor of the epididymis (EAT) is a neoplasm located in the paratesticular region. Mesothelial origin has been mentioned and inflammation has played some role in the development of these tumors. Physical examination and testicular ultrasound constituted important tools in the diagnosis. Some reports have mentioned malignant behavior, but it is very rare. Surgical treatment is the...
Congenital pulmonary airway malformation (CPAM), previously referred to as congenital cystic adenomatoid malformation (CCAM), is a developmental malformation of the lower respiratory tract and the most commonly reported congenital lung lesion. Affected patients typically present with respiratory distress in the neonatal period from expanding cysts and resulting compression of surrounding lung p...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید