हिर्शस्प्रुंग रोग
द्वारा सहकर्मी समीक्षा की गई Dr Anjum Gandhi, FRCPCHद्वारा अंतिम अपडेट Dr Mary Harding, MRCGPअंतिम अद्यतन 14 Jun 2018
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इस श्रृंखला में:कब्जConstipation in childrenरेशा और रेशा पूरकLaxatives
यह पृष्ठ संग्रहित कर दिया गया है।.
इसकी हाल ही में समीक्षा नहीं की गई है और यह अद्यतन नहीं है। बाहरी लिंक और संदर्भ अब काम नहीं कर सकते हैं।.
हिर्शस्प्रुंग रोग एक ऐसी स्थिति है जिसमें आंत (गट) के एक हिस्से में कुछ नसें गायब होती हैं। इसके परिणामस्वरूप आंत की मांसपेशियाँ उस हिस्से में ठीक से संकुचित नहीं हो पातीं। इसलिए वे उस हिस्से से मल को बाहर नहीं निकाल पातीं। मल फंस जाता है जिससे रुकावट (अवरोध) होती है। यह समस्या आमतौर पर जीवन के शुरुआती चरण में ही स्पष्ट हो जाती है क्योंकि यह गंभीर कब्ज का कारण बनती है। इसे ठीक करने का एकमात्र तरीका ऑपरेशन है।.
एक नजर में
Hirschsprung's disease is a rare condition present from birth where part of the bowel lacks nerves.
This causes problems with constipation and tummy swelling because poo cannot move along the bowel.
Symptoms often appear in the first few days of a baby's life, but can be less severe in some cases.
Diagnosis usually involves a biopsy to check for missing nerve cells in the bowel.
Treatment is an operation to remove the affected part of the bowel.
Seek urgent medical advice if your child develops a high temperature, tummy pain, or horrible-smelling or bloody diarrhoea.
इस लेख में:
के लिए वीडियो चयन Genetic conditions
नीचे पढ़ना जारी रखें
What causes Hirschsprung's disease?
In Hirschsprung's disease, a section of the gut (bowel) does not work properly. Usually it is a small section towards the very end of the bowel which is affected. It is not known why this is the case, but it seems to be a failure of development of the nerves in one part of the bowel while the baby is in the womb.
The defect may be inherited through genes passed on from parents. It is more common in children who have a family member who has been affected by Hirschsprung's disease. It is sometimes associated with other genetic conditions such as डाउन सिंड्रोम. There is no obvious genetic cause in many cases, however.
The nerves control the muscles of the inside wall of the bowel tube. Without the nerves, the muscles do not contract. Without the squeezing effect of the muscle contractions, poo is not moved along the bowel, so it gets stuck.
Who gets Hirschsprung's disease?
सामग्री पर वापस जाएंHirschsprung's disease is a condition which is present from birth. Usually this malfunction of the bowel causes problems immediately, so the condition becomes apparent in the first few days of life. So it is most commonly diagnosed in newborn babies. However, if a very small section of the bowel is affected, symptoms may be less severe. If this is the case, the diagnosis may not be made until the children are a little bit older. Very rarely it is diagnosed in adults.
Hirschsprung's disease is rare. About 1 in 5,000 babies have the condition. As mentioned above, it is more common in babies with Down's syndrome. About 1 in 11 babies with Hirschsprung's disease also have Down's syndrome, and babies with Down's syndrome have about 40 times the chance of having Hirschsprung's disease. There are also associations with other rare genetic conditions.
नीचे पढ़ना जारी रखें
Hirschsprung's disease symptoms
सामग्री पर वापस जाएंThe symptoms from Hirschsprung's disease come from poo getting stuck, and the effects that brings. So there is constipation - ie no poo is passed, or it is passed with extreme difficulty. That leads to tummy swelling और tummy pain. In many cases, this is a problem within the first day or two after the baby is born. They may not pass any poo at all after being born. Some babies with Hirschsprung's disease do, however, start off by passing some dark green new baby poo (meconium), but then start having problems a few days, weeks or months later. If the blockage becomes very severe, the baby may start bringing up (vomiting) a green or brown fluid.
If the condition is not severe enough to be apparent early on, the symptoms may not be so obvious. An older child with Hirschsprung's disease may have long-standing constipation, tiredness, tummy pains and poor growth. It may be difficult to get them out of nappies as they may have incontinence due to an overflow of poo leaking round the blockage.
If Hirschsprung's disease is not diagnosed, the first sign of it may be a complication called enterocolitis. This is an infection of the guts which is very serious. If not treated quickly, it can lead on to life-threatening complications such as leaking of the bowel wall (perforation) or sepsis. Symptoms of enterocolitis include a high temperature (fever), tummy pain and horrible-smelling diarrhoea, which sometimes contains blood.
What tests are needed?
सामग्री पर वापस जाएंA tummy (abdominal) X-ray usually shows there is a blockage. It shows loops of swollen guts. A blood test may be done to check for infection (enterocolitis).
In order to make the diagnosis, a biopsy is needed from the very lower end of the bowel (rectum). A biopsy is a procedure in which a small sample of tissue is taken from the affected area and examined under a microscope. If the diagnosis is Hirschsprung's disease, it will be apparent that the normal nerve cells are not present. Often a general anaesthetic will be needed to perform this test.
In older children or adults, other tests are sometimes used. These include an X-ray with a contrast substance (called a barium enema) or tests of the bowel muscles (anal manometry).
नीचे पढ़ना जारी रखें
Hirschsprung's disease treatment
सामग्री पर वापस जाएंThe treatment for Hirschsprung's disease is an operation to remove the part of the gut which is not working. The normal gut is then re-connected. Sometimes this can't be done at the same time, in which case a temporary stoma is formed during the operation. A stoma is an opening in the tummy wall which allows stool to pass directly into a pouch worn on the body. In time, another operation is done to connect the ends of the bowel inside the tummy so that the stoma is no longer needed. It will depend on how old your baby or child is, and how unwell they are. Your specialists will advise on the best course of action and will explain exactly what it involves.
Sometimes if a baby is too unwell for an operation, in the short term they can be treated with bowel washouts to clear the poo. The operation will be needed at some stage however.
What is the outlook?
सामग्री पर वापस जाएंIf Hirschsprung's disease is diagnosed and treated promptly, the outlook (prognosis) is good. The operation is usually very successful. As with any operation, however, there are risks, and your specialist will explain these to you. There is a small chance that there will be complications of the anaesthetic or the operation. After recovery, most children will have no further problems, although toilet training may take longer than usual. However, about 1 in 10 will have ongoing problems with constipation. A very few will have long-standing problems controlling their poo and be incontinent.
The most serious complication is infection of the guts (enterocolitis) and this can occur even some years after the operation. Seek urgent medical advice if your child has symptoms of a tummy bug, particularly any of the following:
Blood in the poo.
Horrible smelling diarrhoea.
A high temperature (fever).
Tummy pain.
A swollen tummy.
रोगी के लिए चयन Genetic conditions

बच्चों का स्वास्थ्य
Congenital heart disease
Congenital heart disease is a condition where an abnormality (defect) develops in the heart before birth. There are a number of types of congenital heart defect. Some are mild and cause few problems; others are life-threatening for the baby.
डॉ. मैरी हार्डिंग, MRCGP द्वारा

बच्चों का स्वास्थ्य
Congenital pulmonary airway malformation
Congenital pulmonary airway malformation (CPAM) is a rare abnormality of lung development. It is found either in unborn babies or in young babies. The name has recently changed from congenital cystic adenomatoid malformation (CCAM). It is increasingly detected by the routine ultrasound scan during pregnancy. Congenital means present from birth. Pulmonary means related to the lungs. The severity of the abnormality is very variable. Some lesions can shrink or even disappear without treatment. Some lesions cause the baby to have breathing problems very soon after birth. Some lesions cause severe problems for the baby and may have a poor outcome.
डॉ. हेले विलासी, FRCGP द्वारा
अक्सर पूछे जाने वाले प्रश्न
If Hirschsprung's disease is inherited, can I do anything to prevent it in my baby?
Hirschsprung's disease is a developmental issue that occurs while the baby is in the womb, and it can be inherited. However, there's no information in the article about preventing its occurrence, as it's a structural defect in the bowel's nerve development.
What is meconium and why is it important for diagnosing Hirschsprung's disease?
Meconium is the dark green new baby poo. In the context of Hirschsprung's disease, some babies might pass meconium initially, but then develop problems later. However, a common early sign of the condition is not passing any poo (meconium) at all within the first day or two after birth.
Are there different levels of severity for Hirschsprung's disease based on the affected bowel section?
Yes, if only a very small section of the bowel is affected, the symptoms may be less severe. In such cases, the diagnosis might not be made until the child is a bit older, in contrast to cases where more significant sections are affected and symptoms appear immediately after birth.
What is a stoma and how does it help a baby with Hirschsprung's disease?
A stoma is an opening created in the tummy wall during an operation. It allows stool to pass directly into a pouch worn on the body. This is a temporary measure sometimes used when the normal gut cannot be re-connected immediately, often due to the baby's age or how unwell they are. A second operation is then performed later to connect the bowel ends, making the stoma no longer necessary.
Can Hirschsprung's disease only affect babies and young children, or can adults also be diagnosed?
While Hirschsprung's disease usually becomes apparent in newborn babies due to immediate problems, if a very small section of the bowel is affected, symptoms may be less severe. In these cases, diagnosis might not occur until children are a little older. Very rarely, it can even be diagnosed in adults.
What types of ongoing problems might arise after successful surgery for Hirschsprung's disease?
After recovery from surgery, most children have no further problems, though toilet training might take longer than usual. However, about 1 in 10 children will experience ongoing constipation. A very small number might have long-standing issues with controlling their poo and could be incontinent. The most serious ongoing complication is enterocolitis, an infection of the guts, which can occur years after the operation.
अधिक पठन और संदर्भ
- Kessmann J; Hirschsprung's disease: diagnosis and management. Am Fam Physician. 2006 Oct 15;74(8):1319-22.
- Bradnock TJ, Knight M, Kenny S, et al; Hirschsprung's disease in the UK and Ireland: incidence and anomalies. Arch Dis Child. 2017 Aug;102(8):722-727. doi: 10.1136/archdischild-2016-311872. Epub 2017 Mar 9.
- Gosain A, Frykman PK, Cowles RA, et al; Guidelines for the diagnosis and management of Hirschsprung-associated enterocolitis. Pediatr Surg Int. 2017 May;33(5):517-521. doi: 10.1007/s00383-017-4065-8. Epub 2017 Feb 2.
नीचे पढ़ना जारी रखें
लेखक के बारे मेंपूरा जीवन परिचय देखें

Dr Mary Harding, MRCGP
सामान्य चिकित्सक, चिकित्सा लेखक
BA, MA, MB, BChir, MRCGP, DFFP
डॉ मैरी हार्डिंग ने 1989 में कैम्ब्रिज विश्वविद्यालय के मेडिकल स्कूल से योग्यता प्राप्त की।.
समीक्षक के बारे मेंपूरा जीवन परिचय देखें

Dr Anjum Gandhi, FRCPCH
Consultant Paediatrician
MBBS, MD, MRCP, FRCPCH
Dr. Anjum Gandhi has over 25 years of clinical, teaching and research experience in paediatrics and is a Consultant Paediatrician.
लेख का इतिहास
इस पृष्ठ पर दी गई जानकारी योग्य चिकित्सकों द्वारा लिखी और सहकर्मी समीक्षा की गई है।.
14 Jun 2018 | नवीनतम संस्करण

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