Noninvoluting congenital hemangiomas with hypovolemic shock, anemia and prolonged jaundice in a neonate: a case report.

Noninvoluting congenital hemangioma is an extremely rare congenital anomaly in newborn babies and may complicate life-threatening events, including hemorrhage. We present a very rare case of noninvoluting congenital hemangiomas in an Asian and Afghan six-day-old girl that was detected at birth. The noninvoluting congenital hemangiomas were accompanied by hypovolemic shock, anemia, and prolonged jaundice during the first two weeks of life.

Bland White Garland syndrome with aneurysm and collaterals of coronary arteries in an Afghan girl: a case report.

Bland White Garland Syndrome is a very rare congenital heart defect in which the left coronary artery arises abnormally from the pulmonary artery. We present an extremely rare case of Bland White Garland Syndrome with an aneurysm of the left coronary artery in a 14-year-old Afghan girl. The patient was asymptomatic throughout her life except for one attack of exertional chest discomfort.

The Impact of Negative Moral Character on Health and the Role of Spirituality: A Narrative Literature Review.

Although negative moral character is highly prevalent, it is not included in the International Classification of Diseases (ICD). Along with the modification of WHO ICD-11, spirituality should be acknowledged for its potetnial role in the prevention of negative moral traits. This study aimed to explore the effects of negative moral character on health and determine the role of spirituality in improving negative moral traits.

Right-side diaphragmatic eventration with atrial septa defect and cleft palate in an infant: a case report.

Background: Congenital right-side diaphragmatic eventration with atrial septal defect and cleft palate is a rare congenital anomaly.

Case Presentation: We present a rare case of congenital right-sided diaphragmatic eventration along with atrial septal defect, cleft palate, pneumonia, and undernutrition in a 3-month-old Asian and Afghan girl. The clinical features were observed in the third month of life, and the diagnosis of these anomalies was established by the patient's history, physical examination, chest X-ray, thoracic computed tomography, and echocardiography.

A challenging high-risk surgery for necrotizing pneumonia in a right bilobed lung.

Background: Necrotizing pneumonia is rare in children and is one of the most serious complications of a lung infection caused by antibiotic failure. We present a 12-year-old leukopenic child with a long-lasting lung infection, presenting as having a lung hydatid cyst, but diagnosing with necrotizing pneumonia in the right bilobed lung. Failure to medical treatment and ongoing leukopenia justified surgical intervention with positive results.

Left lung aplasia with patent ductus arteriosus in a term newborn baby: a case report.

Pulmonary aplasia is a very rare congenital anomaly identified by the absence of lung parenchyma or vessels. This malformation mostly accompanies other anomalies, and chest computed tomography (CT) is a useful diagnostic tool. We present a rare case of left lung aplasia with patent ductus arteriosus and neonatal sepsis in a term newborn baby who had respiratory distress.