Meissner's plexus (submucosal plexus) is one of two major components of the enteric nervous system (alongside Auerbach's myenteric plexus), located in the submucosal layer of the gastrointestinal tract from the esophagus to the rectum. It contains sensory neurons (monitoring luminal content), secretomotor neurons (controlling mucosal secretion), and neurons modulating absorptive epithelial function. It works with the myenteric plexus to coordinate gut motility, secretion, and blood flow.
Meissner's plexus is pathologically involved in Hirschsprung's disease: congenital absence of ganglion cells extends from the rectum proximally (usually to the rectosigmoid) through both myenteric and submucosal plexuses, producing a functional obstruction from tonic smooth muscle contraction without normal peristaltic relaxation. Diagnosis by rectal suction biopsy (sampling the submucosal layer for presence of ganglion cells) is the gold standard. Hirschsprung's disease treatment (Swenson, Soave, or Duhamel pull-through) removes the aganglionic segment and brings normally-innervated bowel to the anus.
Failure of neural crest cell migration into the distal bowel produces absence of both myenteric and submucosal plexus ganglion cells, causing the aganglionic bowel segment to maintain tonic contraction without peristaltic relaxation; rectal suction biopsy confirms the absence of submucosal ganglia and identifies the transition zone between ganglionic and aganglionic bowel.
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