A 33-year-old man had dizziness for 3 days without provoking factors. Head CT demonstrated a mass in the left lateral anterior cranial fossa with calcification and cystic degeneration (figure 1, A–C). MRI showed an irregularly shaped mass with mixed signal and slight marginal enhancement (figure 1, D–F). He underwent mass resection with no recurrent dizziness during 12 months’ follow-up. On pat...

Gastric duplication cysts (GDC) lined with pseudostratified columnar ciliated epithelium (PCCE) are uncommon lesions that stem from a foregut developmental malformation. The clinical and radiological diagnosis is usually difficult. Definitive diagnosis can be established by histopathological examination. In this study, we report a rare case of a peri-gastric mass that was operated and reported ...

There is a broad spectrum of bronchopulmonary malformations which present in early infancy and childhood. These include Bronchogenic cysts, Bronchopulmonary sequestrations, congenital cystic adenomatoid malformation (CCAM), and congenital lobar emphysema. These lesions maybe detected by prenatal diagnosis, present as acute respiratory distress in the newborn period, or may remain undiagnosed an...

INTRODUCTION Congenital cystic adenomatoid malformation of the lung is an uncommon cause of respiratory distress in neonates and babies. The disorder is usually diagnosed in the neonatal period and the first two years of life. This anomaly has been described in association with bronchopulmonary sequestration, extralobar intra-abdominal sequestration or bronchial atresia in live and stillborn ba...

Pulmonary sequestration is a rare congenital malformation of lung in which part the supplied by an anomalous systemic blood supply from thoracic or abdominal aorta. This nonfunctioning tissue and lacks normal communication with tracheobronchial tree. It develops accessory bud. If developed before pleura formation, it results intralobar sequestration, extralobar, if after formation. Usually Intr...

PURPOSE We reviewed the cases of 33 patients from our clinic and 142 patients from the literature with congenital bronchopulmonary vascular malformations (BPVM), systematically analyzed the bronchopulmonary airways, pulmonary arterial supplies, and pulmonary venous drainages, and classified these patients by pulmonary malinosculation (PM). MATERIALS AND METHODS From January 1990 to January 20...

The anesthesia ex utero intrapartum treatment (EXIT) procedure is a specialized surgical procedure used to deliver babies who have airway compression due to cystic adenomatoid malformation, bronchopulmonary sequestration, cervical teratomas, or other congenital conditions. EXIT is erroneously known as a routine cesarean section (CS), but is rather an extension of CS with discernible differences...

Congenital lobar emphysema is an uncommon bronchopulmonary malformation characterized by lobar overinflation and accompanying alveolar septum damage that leads to compression atelectasis of the lung parenchyma and displacement of mediastinal structures, with the resultant ventilation-perfusion mismatch. We present a case of a 33-year-old lady with progressive exertional dyspnea. Chest radiograp...