Megacolon
Congenital megacolon Congenital aganglionosis, Hirschsprung's disease A disease affecting 1:5000 live births, with a sibling risk of 1% for girls and 5% for boys; Hirschsprung's disease–HD is ten-fold more common in Down syndrome; other anomalies in HD include hydrocephalus, VSD, cryptorchism, diverticulosis of the urinary bladder, renal cysts and agenesis, polyposis coli, Laurence-Moon-Biedl syndrome Treatment Resection of aganglionic colon
Acquired megacolon A condition related to narcotics or disruption of ganglionic innervation–eg idiopathic hypomotility, neuropathies–parkinsonism, multiple sclerosis, myotonic dystrophy, diabetic neuropathy, Chagas' disease, smooth muscle disorders–amyloidosis and progressive systemic sclerosis and metabolic disease–hypokalemia, lead poisoning, porphyria, pheochromocytoma, hypothyroidism and may be due to intraluminal overgrowth of microorganisms in Crohn's disease and ulcerative colitis–toxic megacolon–characterized by mucosal necrosis, transmural inflammation and systemic 'toxicity' associated with high fever, tachycardia, leukocytosis and diarrhea; in psychogenic megacolon, no radiologic or pathologic defects are present–the condition may be related to a 'fixation' in Freud's anal retentive stage of psychosexual development, with constipation of later onset than in HD, possibly 2º to abuse of anthracine laxatives