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Ganglion cell rectal cecum imperforate anus

Departments of Paediatric Surgery, Pathology, P. Three cases of type IV congenital pouch colon associated with low anorectal anomaly are reported here. Pouch colon may be a cause of intractable constipation in children operated for low anorectal anomaly. Excellent results can be obtained by exicision of the pouch.
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Colon and Rectum Normal Anatomy and Congenital Variants

Ganglion cell rectal cecum imperforate anus
Ganglion cell rectal cecum imperforate anus
Ganglion cell rectal cecum imperforate anus
Ganglion cell rectal cecum imperforate anus
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(PDF) Patients with Anorectal Malformation and Hirschsprung's Disease

Imperforate Anus or Anorectal Malformation is a defect spotted at birth in which the anal opening is either blocked or is entirely missing. According to researchers, this abnormality exists in 1 out of every births. This is found mostly in boys than girls. This condition usually develops in utero between the fifth and seventh weeks of pregnancy. There is no known cause for Imperforate Anus, but this condition may be associated with certain other defects of the rectum. Diagnosis of Imperforate Anus is generally made just after birth. It is a potentially serious condition and requires immediate treatment.
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Patients with Anorectal Malformation and Hirschsprung's Disease

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Abdominal Imaging pp Cite as. The gastrointestinal tract terminates at the colon, which is involved in absorption of water and electrolytes, mucus secretion, and the propagation and storage of fecal material. The colon measures approximately — cm in length and comprises one-fifth of the total intestinal length. It begins just distal to the terminal ileum at the ileocecal valve and extends to the dentate line, which includes the proximal two-thirds of the anal canal. Skip to main content.
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