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Hirschsprung disease Hirschsprung Disease Hirschsprung disease (HD), also known as congenital aganglionosis or congenital megacolon, is a congenital anomaly of the colon caused by the failure of neural crest-derived ganglion cells to migrate into the distal colon. The lack of innervation always involves the rectum and extends proximally and contiguously over variable distances. M Hirschsprung Disease (HD), also known as congenital Congenital Chorioretinitis aganglionosis or congenital Congenital Chorioretinitis megacolon Megacolon Megacolon is a severe, abnormal dilatation of the colon, and is classified as acute or chronic. There are many etiologies of megacolon, including neuropathic and dysmotility conditions, severe infections, ischemia, and inflammatory bowel disease. Megacolon, is a congenital Congenital Chorioretinitis anomaly of the colon Colon The large intestines constitute the last portion of the digestive system. The large intestine consists of the cecum, appendix, colon (with ascending, transverse, descending, and sigmoid segments), rectum, and anal canal. The primary function of the colon is to remove water and compact the stool prior to expulsion from the body via the rectum and anal canal. Colon, Cecum, and Appendix: Anatomy caused by the failure of neural crest-derived ganglion cells Ganglion Cells The Visual Pathway and Related Disorders to migrate into the distal colon Colon The large intestines constitute the last portion of the digestive system. The large intestine consists of the cecum, appendix, colon (with ascending, transverse, descending, and sigmoid segments), rectum, and anal canal. The primary function of the colon is to remove water and compact the stool prior to expulsion from the body via the rectum and anal canal. Colon, Cecum, and Appendix: Anatomy. The lack of innervation always involves the rectum Rectum The rectum and anal canal are the most terminal parts of the lower GI tract/large intestine that form a functional unit and control defecation. Fecal continence is maintained by several important anatomic structures including rectal folds, anal valves, the sling-like puborectalis muscle, and internal and external anal sphincters. Rectum and Anal Canal: Anatomy and extends proximally and contiguously over variable Variable Variables represent information about something that can change. The design of the measurement scales, or of the methods for obtaining information, will determine the data gathered and the characteristics of that data. As a result, a variable can be qualitative or quantitative, and may be further classified into subgroups. Types of Variables distances. Most cases are diagnosed in the neonatal period, with a classic triad of symptoms including delayed passage of meconium Meconium The thick green-to-black mucilaginous material found in the intestines of a full-term fetus. It consists of secretions of the intestinal glands; bile pigments; fatty acids; amniotic fluid; and intrauterine debris. It constitutes the first stools passed by a newborn. Prenatal and Postnatal Physiology of the Neonate, abdominal distension, and bilious vomiting Bilious Vomiting Congenital Duodenal Obstruction. Individuals having less severe degrees of functional obstruction may not be diagnosed until later in infancy or childhood when they present with symptoms of chronic refractory constipation Constipation Constipation is common and may be due to a variety of causes. Constipation is generally defined as bowel movement frequency < 3 times per week. Patients who are constipated often strain to pass hard stools. The condition is classified as primary (also known as idiopathic or functional constipation) or secondary, and as acute or chronic. Constipation, abdominal distension, and failure to thrive Failure to Thrive Failure to thrive (FTT), or faltering growth, describes suboptimal weight gain and growth in children. The majority of cases are due to inadequate caloric intake; however, genetic, infectious, and oncological etiologies are also common. Failure to Thrive. The diagnosis of HD is confirmed by the absence of ganglion cells Ganglion Cells The Visual Pathway and Related Disorders on rectal biopsy Biopsy Removal and pathologic examination of specimens from the living body. Ewing Sarcoma after noninvasive testing such as anorectal manometry Anorectal Manometry Pediatric Constipation and the use of contrast enema. Surgical resection of the aganglionic segment is the standard treatment.
Last updated: Mar 4, 2024
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Hirschsprung disease Hirschsprung Disease Hirschsprung disease (HD), also known as congenital aganglionosis or congenital megacolon, is a congenital anomaly of the colon caused by the failure of neural crest-derived ganglion cells to migrate into the distal colon. The lack of innervation always involves the rectum and extends proximally and contiguously over variable distances. M Hirschsprung Disease (HD), also known as congenital Congenital Chorioretinitis aganglionosis or congenital Congenital Chorioretinitis megacolon Megacolon Megacolon is a severe, abnormal dilatation of the colon, and is classified as acute or chronic. There are many etiologies of megacolon, including neuropathic and dysmotility conditions, severe infections, ischemia, and inflammatory bowel disease. Megacolon, is a congenital Congenital Chorioretinitis anomaly of the colon Colon The large intestines constitute the last portion of the digestive system. The large intestine consists of the cecum, appendix, colon (with ascending, transverse, descending, and sigmoid segments), rectum, and anal canal. The primary function of the colon is to remove water and compact the stool prior to expulsion from the body via the rectum and anal canal. Colon, Cecum, and Appendix: Anatomy caused by the failure of neural crest-derived ganglion cells Ganglion Cells The Visual Pathway and Related Disorders to migrate into the distal colon Colon The large intestines constitute the last portion of the digestive system. The large intestine consists of the cecum, appendix, colon (with ascending, transverse, descending, and sigmoid segments), rectum, and anal canal. The primary function of the colon is to remove water and compact the stool prior to expulsion from the body via the rectum and anal canal. Colon, Cecum, and Appendix: Anatomy.
The pathophysiology in HD is the complete absence of ganglion cells Ganglion Cells The Visual Pathway and Related Disorders (aganglionosis) in the intrinsic nerve supply of the bowel due to the failure of neural crest-derived ganglion cells Ganglion Cells The Visual Pathway and Related Disorders to migrate completely into the myenteric plexuses of the wall of the colon Colon The large intestines constitute the last portion of the digestive system. The large intestine consists of the cecum, appendix, colon (with ascending, transverse, descending, and sigmoid segments), rectum, and anal canal. The primary function of the colon is to remove water and compact the stool prior to expulsion from the body via the rectum and anal canal. Colon, Cecum, and Appendix: Anatomy.[1,2,6–8]
Most individuals with HD are diagnosed in the 1st month of life. Individuals with less severe disease may not present with symptoms until 3 years of age in approximately 10% of cases.[2,6,9]
If HD is suspected based on the clinical presentations in the neonatal or postnatal periods, the following diagnostic tests Diagnostic tests Diagnostic tests are important aspects in making a diagnosis. Some of the most important epidemiological values of diagnostic tests include sensitivity and specificity, false positives and false negatives, positive and negative predictive values, likelihood ratios, and pre-test and post-test probabilities. Epidemiological Values of Diagnostic Tests are used:
Approach in diagnosis[12]
Constipation Constipation Constipation is common and may be due to a variety of causes. Constipation is generally defined as bowel movement frequency < 3 times per week. Patients who are constipated often strain to pass hard stools. The condition is classified as primary (also known as idiopathic or functional constipation) or secondary, and as acute or chronic. Constipation with suspicious features of HD (delayed meconium Meconium The thick green-to-black mucilaginous material found in the intestines of a full-term fetus. It consists of secretions of the intestinal glands; bile pigments; fatty acids; amniotic fluid; and intrauterine debris. It constitutes the first stools passed by a newborn. Prenatal and Postnatal Physiology of the Neonate passage, squirt sign, abdominal distention Abdominal distention Megacolon in infants, or refractory constipation Constipation Constipation is common and may be due to a variety of causes. Constipation is generally defined as bowel movement frequency < 3 times per week. Patients who are constipated often strain to pass hard stools. The condition is classified as primary (also known as idiopathic or functional constipation) or secondary, and as acute or chronic. Constipation in patients Patients Individuals participating in the health care system for the purpose of receiving therapeutic, diagnostic, or preventive procedures. Clinician–Patient Relationship 6 months to 3 years old):
Genetic testing Genetic Testing Detection of a mutation; genotype; karyotype; or specific alleles associated with genetic traits, heritable diseases, or predisposition to a disease, or that may lead to the disease in descendants. It includes prenatal genetic testing. Myotonic Dystrophies[9]
Hirschsprung disease as seen on contrast barium enema study, with the arrow showing the “transition zone” between the normal and aganglionic bowel
Image: “Contrast enema showing a CETZ at rectosigmoid, arrow” by Pratap, A., et al. License: CC BY 2.0, cropped by Lecturio.Diagrammatic outcomes of the 3 common pull-through procedures for Hirschsprung disease. A: Internal sphincter. B: External sphincter. C: Cuff of the muscularis propria retained in Soave procedure. In the Swenson procedure, the aganglionic segment and transition zone are pulled through the anus and resected. The transected end of ganglionic bowel proximal to the aganglionic segment is sutured end to end to the terminal rectum. In the Soave procedure, the initial radial incision is made through the mucosa, and the dissection is extended proximally in the submucosal plane for several centimeters before dividing the muscularis propria. As a consequence, the muscularis propria of the distal rectum is retained as a “cuff,” through which the ganglionic bowel is drawn inferiorly and attached just above the dentate line. This avoids dissection in the pelvis, thus decreasing risk of pelvic nerve injury. In the Duhamel procedure, the ganglionic bowel is attached in a side-to-side manner to the posterior rectum. The anterior rectum remains as an aganglionic pouch.
Image by Lecturio.Causes of intestinal obstruction Intestinal obstruction Any impairment, arrest, or reversal of the normal flow of intestinal contents toward the anal canal. Ascaris/Ascariasis in the neonatal period can be distinguished from HD based on their clinical features and the presence of ganglia on a rectal biopsy Biopsy Removal and pathologic examination of specimens from the living body. Ewing Sarcoma.
Causes of intestinal obstruction Intestinal obstruction Any impairment, arrest, or reversal of the normal flow of intestinal contents toward the anal canal. Ascaris/Ascariasis in older infants and children: