Congenital fistula of rectum and anus digital illustration

Congenital fistula of rectum and anus Save


ICD-10 code: Q43.6

Disease category: Q43: Other congenital malformations of intestine

Congenital Fistula of Rectum and Anus: Understanding the Condition

Congenital fistula of the rectum and anus, also known as anorectal malformation, is a birth defect that affects the lower gastrointestinal tract. It occurs when the rectum and anus don't develop properly during fetal development. This condition can lead to various complications and requires medical attention for proper management.

While the exact cause of congenital fistula of the rectum and anus is unknown, it is believed to be a combination of genetic and environmental factors. Certain genetic mutations and maternal health conditions may increase the risk of this condition in newborns.

Common symptoms of congenital fistula of the rectum and anus include an abnormal opening in the anus, absence of a normal anal opening, or the presence of a small opening in the wrong location. These symptoms can vary in severity, depending on the specific type and complexity of the malformation.

  1. Rectovestibular Fistula: This is the most common type, where the rectum connects to the vestibule (the area between the vaginal opening and the anus) in females.
  2. Rectourethral Fistula: In males, the rectum connects to the urethra, the tube that carries urine from the bladder.
  3. Rectobladderneck Fistula: This type involves a connection between the rectum and the neck of the bladder.

Diagnosing congenital fistula of the rectum and anus usually occurs soon after birth. A physical examination by a pediatric surgeon or gastroenterologist is necessary to determine the specific type of malformation. Additional tests, such as X-rays, ultrasound, or an MRI, may be performed to assess the exact anatomy and associated complications.

It's important to note that the treatment for congenital fistula of the rectum and anus varies depending on the complexity of the malformation. Surgery is often required to repair the defect and restore normal bowel function. However, discussing treatment options and potential outcomes with a healthcare professional is crucial.

Regular follow-up appointments with a specialist are necessary to monitor the child's growth, development, and bowel function. Additional support may be required to address potential long-term complications, such as bowel control issues or urinary problems.

In conclusion, congenital fistula of the rectum and anus is a birth defect affecting the lower gastrointestinal tract. Understanding the symptoms, diagnosis, and available treatment options can help parents and caregivers navigate this condition and provide the necessary care and support for affected children.

Treatment of Congenital fistula of rectum and anus:

Congenital Fistula of Rectum and Anus: Understanding Treatment Options

Congenital fistula of the rectum and anus is a rare condition that affects infants at birth. It refers to an abnormal connection between the rectum and the skin surrounding the anus. This condition requires timely medical intervention to ensure proper functioning of the digestive system and overall well-being of...

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