Analatresie

Anal atresia, or imperforate anus, refers to a spectrum of anorectal abnormalities ranging from a membranous separation to complete absence of the anus.

Epidemiology

The estimated incidence is 1 in 5000 live births.

Pathology

Clinically there is no anal opening. Subtypes can be classified into two broad categories: high (supralevator) or low (infralevator), depending on the location of the atretic portion.

Genetics

Most cases are sporadic, with occasional familial forms

Associations

There are frequent associations with other congenital abnormalities.

• other atresias
  • esophageal atresia
• VACTERL association
• caudal regression syndrome: associated sacral agenesis and lower limb hypoplasia
• Currarino's triad; anorectal malformations with sacral anomalies and presacral mass lesion
• fistulous tracts to the urethra or vagina may be present or may have a single cloacal opening

Radiographic features

Abdominal radiograph

• can be variable depending on the site of atresia (i.e. high or low), level of meconium impaction and physiological effects such as straining
• may show multiple dilated bowel loops with an absence of rectal gas

• air within urinary bladder suggests high type

• calcified meconium in the bowel loops would suggest high type (meconium calcifies due to urine exposure)

Invertogram

A coin/metal piece is placed over the expected anus and the baby is turned upside down (for a minimum 3 minutes).

The distance of the gas bubble in the rectum from the metal piece is noted:

• >2 cm denotes high type
• <2 cm denotes low type

False-positive: if image is taken in the 1^st 24 hours of life or impacted meconium in distal rectum .

For radiographic technique, see invertogram view and prone cross-table lateral view articles.

Fluoroscopy (contrast study)

• to detect a rectourinary, rectovaginal, or rectoperineal fistula
• the fistula is considered low (below the levator ani plane) if it is below the pubococcygeal line and high if above it

Ultrasound

• the anus may be seen as an echogenic spot at the level of the perineum and in anal atresia, this echogenic spot may be absent
• may show bowel dilatation
• an infracoccygeal or transperineal approach may allow differentiation between high and low subtypes
• kidneys should be assessed in such patients
• spinal US can reveal spinal cord lesions like tethering of cord

MRI

Can be used pre/postoperatively to study pelvic floor, renal and spinal abnormalities .

Treatment and prognosis

• low subtypes are treated with anoplasty   
• high subtypes are treated with colostomy with subsequent potential repair  

Complications

• meconium peritonitis

See also

• duodenal atresia
• small bowel atresia

Siehe auch:

• Ösophagusatresie
• caudal regression syndrome
• VACTERL-Assoziation
• Duodenalatresie
• Invertogramm nach Wangensteen-Rice
• Mekoniumperitonitis
• Stratton-Parker-Syndrom
• small bowel atresia

und weiter:

• Down-Syndrom
• congenital tracheo-oesophageal fistula
• Ileumatresie
• caudal dysplasia sequence
• VATER
• OEIS complex
• ASP-Assoziation
• VATER anomaly
• esophageal atresia with H-type tracheo-esophageal fistula
• McKusick-Kaufman-Syndrom
• Pallister-Hall-Syndrom
• Atresie
• fetal bowel dilatation
• IVIC-Syndrom
• fetal colonic dilatation
• H-type tracheo-oesophageal fistula with no atresia
• Schmid-Fraccaro-Syndrom
• anorektale Stenosen
• antenatale Darmperforation
• Kolonatresie