disease | Anal Atresia |
alias | Anal Atresia, Low Anorectal Atresia, Anal Closure |
Anal atresia, also known as low anorectal atresia, occurs due to abnormal development of the primitive anus, resulting in the failure to form an anal canal and causing the rectum to be disconnected from the outside. In Chinese medicine, it is referred to as "anal closure."
bubble_chart Etiology
Imperforate anus is a type of mid-level malformation commonly seen in clinical practice. Due to developmental disorders of the primitive anus, it fails to invaginate and form the anal canal. The development of the rectum is generally normal, with its blind end located near the edge of the bulbospongiosus muscle of the urethra or the lower end of the vagina, and the puborectalis muscle surrounds the distal end of the rectum. The perineum is often underdeveloped, appearing flat, and the anal region is covered with intact skin. It may be associated with fistulas in the bulb of the urethra, the lower segment of the vagina, or the vestibule.
bubble_chart Clinical Manifestations
After birth, the infant did not pass meconium and quickly developed symptoms of intestinal obstruction such as vomiting, abdominal distension, and fullness. Upon local examination, the perineal center appeared flat, with the anal area partially covered by skin. In some cases, there was a small, pigmented dimple with radiating wrinkles, and stimulation of this area elicited a contraction response of the sphincter muscle. When the infant cried or strained, a bulge appeared in the center of the perineum, and placing a finger in this area could feel an impulse. When the infant was placed in a head-down position with the buttocks elevated, percussion over the anal region produced a tympanic sound.
bubble_chart DiagnosisAfter birth, there is no passage of meconium, and the anal area is covered by skin. There is a sense of impact in the anal area when crying. On an inverted lateral X-ray, the distal end of the rectum is located at or slightly below the pubococcygeal line. Ultrasound and puncture methods indicate that the rectal blind end is approximately 1.5 cm from the anal skin.
bubble_chart Treatment Measures
Surgery should be performed as soon as possible after diagnosis, generally by perineal anoplasty, or alternatively by sacroperineal anoplasty.
Perineal Anoplasty (Figure 1):
⑴ Incision
⑵ Separation through the middle of the sphincter
⑶ Freeing the rectal blind end
⑷ Anoplasty
Figure 1 Perineal Anoplasty