Tracheoesophageal fistula
Tracheoesophageal fistula (TEF) is a congenital or acquired condition where an abnormal connection (fistula) exists between the esophagus and the trachea. TEF is a critical condition that requires immediate medical attention.
Causes[edit | edit source]
TEF is often congenital, meaning it is present at birth. The exact cause of congenital TEF is unknown, but it may be related to various genetic factors or exposure to certain substances during pregnancy. Acquired TEF can occur due to injury, infection, or cancer.
Symptoms[edit | edit source]
Symptoms of TEF may include difficulty swallowing (dysphagia), coughing or choking during feeding, cyanosis (bluish coloration of the skin due to lack of oxygen), and recurrent lung infections.
Diagnosis[edit | edit source]
Diagnosis of TEF is typically made through a combination of physical examination, medical history, and imaging tests. These may include X-rays, CT scans, or MRIs. In some cases, a bronchoscopy or esophagoscopy may be performed to visualize the fistula.
Treatment[edit | edit source]
Treatment for TEF usually involves surgery to repair the fistula. This is typically performed shortly after birth in cases of congenital TEF. In cases of acquired TEF, treatment may also involve addressing the underlying cause of the fistula.
Prognosis[edit | edit source]
The prognosis for individuals with TEF varies depending on the severity of the condition and the presence of other health problems. With prompt and appropriate treatment, many individuals with TEF can lead normal, healthy lives.
See also[edit | edit source]
Tracheoesophageal fistula Resources | |
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Contributors: Prab R. Tumpati, MD