Complications of CD
REMEMBER ALL LINKS ARE IN RED TEXT EXCEPT ON THE NAVIGATION MENU TO THE LEFT
Possible local complications of Crohn's disease include:(remember, links are in red)
intestinal obstruction
hemorrhage
perforation with abscess
stricture formation; common
perianal fistula
fistula to the bowel, bladder, vagina
increased risk of malignancy but less than that of ulcerative colitis.
Common complications include:
weight loss
In general, there are no specific foods that have to be avoided by the Crohn's
patient. Patients should try and eat a balanced diet and avoid food which
upsets them. However, in particular situations then dietary modification
is necessary:
high fibre foods, e.g. fruit and vegetables, may precipitate abdominal pain
in some patients - especially those with small intestinal disease.
In this group of patients a low residue diet, e.g. avoidance of vegetables,
brown bread may bring symptomatic relief
low fat diets: if steatorrhoea is a main complaint
exclusion diet: this is as reliable as corticosteroids in producing
remission in acute disease - success rate as high as 90%; however, most
patients relapse soon after the resumption of a normal diet
fish oil - there is evidence that enteric-coated fish oil preparations
may reduce relapse rate and maintain remission in patients with Crohn's disease
vitamins and minerals: if there are specific nutritional deficiencies
malnourishment: if the patient has active disease or is perioperative
then parenteral nutrition may be indicate
Anemia
Anaemia can be described as a reduction in the haemoglobin concentration
to below 13.5 g per decilitre in an adult male and below 11.5 g per decilitre
in an adult female.
Anaemia is not a disease in itself, but may reflect an underlying disease
process. It may also result from an increase in plasma volume and a
dilutional effect - for example, as occurs during pregnancy.
It can be classified according to the blood film; thus red cells with a
low mean cell volume (MCV) appear small and pale - microcytic; those with
a large MCV appear large and oval shaped - macrocytic. Alternatively, the
red blood cells may be normal in size and shape but may be reduced in number
- normocytic.
Protein-losing enteropathy desribes a condition where a abnormal bowel
mucosa allows increased protein loss.
Primary Sclerosing Cholangitis
Primary sclerosing cholangitis is a disease in which the bile ducts inside
and outside the liver become narrowed due to inflammation and scarring.
This causes bile to accumulate in the liver and can result in damage to
liver cells. Although the exact cause of Primary Sclerosing Cholangitis
is unknown, genetic and immunologic factors appear to play a role.
Primary sclerosing cholangitis has been considered a rare disease,
but recent studies suggest that it is more common than previously thought.
It may occur alone, but approximately 70% of patients have associated
inflammatory bowel disease, particularly ulcerative colitis.
Primary sclerosing cholangitis is more common in men than women.
Initially, many individuals have no symptoms and the disease is detected
because of abnormal laboratory test results, particularly an enzyme test
called alkaline phosphatase. It usually begins in the 30s, 40s, and 50s,
and is commonly associated with fatigue, itching and jaundice. Episodes of
fever and chills from superimposed infection in the bile ducts occasionally
occur and can be distressing symptoms. The diagnosis of Primary sclerosing
cholangitis is made by cholangiography, an X-ray test involving injection
of dye into the bile ducts. This is usually accomplished by an endoscopic
procedure called ERCP (endoscopic retrograde cholangiopancreatography) but
also may be done radiologically or surgically.
The course of the disease is unpredictable for the patient, but is generally
slowly progressive. The patient may have the disease for many years before
symptoms develop. Symptoms may persist at a stable level, be intermittent,
or progress gradually. Liver failure may occur after 7-15 years of disease
or even longer. Approximately 10% of patients who have the disease on a
longstanding basis may develop a superimposed tumor of the bile ducts called
cholangiocarcinoma.
There is currently no specific treatment for primary sclerosing cholangitis.
Research is under way to determine the effectiveness of a number of
medications. The various symptoms of primary sclerosing cholangitis often
respond effectively to medications that control itching, antibiotics when
recurrent infections occur, and vitamins to replace those that are deficient.
In some instances, endoscopic, radiologic, or surgical techniques may be
employed to open major blockages in the common bile duct and improve bile flow.
When progressive liver failure occurs in spite of these measures,
liver transplantation may be indicated. It is associated with a survival
rate of 75% or more and a good quality of life after recovery.
Other complications include"
arthritis - large joints
erythema nodosum Characteristically the lesions are:
painful, palpable, dusky blue nodules or plaques:
up to 5 cm in diameter
on the shins and calves but
may spread to the thighs and arms .
tend to be symmetrical.
lesions resolve over 2 to 4 weeks to produce an appearance similar to bruising
there may be the appearance of new lesions as the old ones resolve
uncommonly, systemic symptoms such as malaise, fever and arthralgia may occur.
Erythema nodosum represents an inflammation of sub-dermal adipose tissue (paniculitis).
The histopathology is distinctive:
early lesions show widening of the connective tissue between lobules
later there is an cellular infiltrate containing lymphocytes, histiocytes and multinucleate giant cells
Eye problems - conjunctivitis, episcleritis, iritis
sacroiliitis - this is unrelated to HLA B27
gall stones, especially of the cholesterol type
Less common:
liver complications - primary sclerosing cholangitis, fatty liver, non-specific hepatitis, pericholangitis.
ankylosing spondylitis - related to HLA B27
pyoderma gangrenosum Pyoderma gangrenosum is an uncommon, ulcerative skin condition which is accompanied by systemic disease in half of cases.
lesions begin in the dermis with secondary necrosis of the epidermis
the first sign is a pustule with surrounding erythema
with time an ulcer develops
the walls of the ulcer are blue and well defined
there may be systemic symptoms and signs such as:
fever
myalgia
arthralgia
carcinoma of the bile ducts and primary sclerosing cholangitis - much less common than in ulcerative colitis
renal complications - ureteric stricture, stones, right hydronephrosis, nephropathy (oxalate, amyloid).
nutritional deficiency - osteomalacia, weakness (potassium, magnesium, vitamin D), lassitude (vitamin B12, folate, iron), rashes (zinc, niacin), alteration of taste (zinc).
systemic amyloidosis - more common in Crohn's than UC
reduced fertility
Here are a few interesting links I found from the CCFA concerning these complications:
Possible Complications
The complications of Crohn's disease and ulcerative colitis (collectively known as inflammatory bowel disease, or IBD) are generally categorized as either local or systemic. The term "local" refers to a complication involving the intestinal tract itself. The term "systemic" (or extraintestinal) refers to complications involving other organs or complications that affect the patient as a whole -- rather than just the bowel.
In uncomplicated IBD, appropriate treatment of inflammation results in clinical improvement. The patient gets better. When a complication occurs, however, the improvement is delayed, and a specific treatment may be needed to target and resolve that complication. It is important for patients and physicians to be acquainted with these complications because early recognition often means more effective treatment. Many of the same complications occur in both Crohn's disease and ulcerative colitis, and are discussed together. Other complications are specific for ulcerative colitis or Crohn's disease.
What Are the Systemic (Extraintestinal) Complications of IBD?
Systemic complications -- which include fever, weakness, and loss of appetite -- are a reflection of the inflammation in the small intestine and/or colon. But there are also some people with IBD who suffer from certain types of arthritis, skin conditions, inflammation of the eye, liver and kidney disorders, and bone loss. Of all the extraintestinal complications, arthritis is the most common. Joint, eye, and skin complications often occur together. For unknown reasons, the extraintestinal or systemic manifestations may predominate in children and even overshadow the intestinal symptoms, which may make diagnosis even more difficult. It is, therefore, important to keep close watch on youngsters who fail to grow or thrive, feel sick, have fever, and complain of general malaise and weakness. These may be systemic manifestations of IBD.
What Causes These Extraintestinal Manifestations?
The cause is not known, but it is believed that all of these complications represent an abnormal response of the immune system (the body's line of defense). As the immune system reacts, it triggers inflammation in other parts of the body -- as well as in the intestine. It is also not known why some individuals are affected and others are not.
For more information about extraintestinal complications, please see the documents below. While you may never have any of these complications, it's important to be aware of them and to see your doctor if you experience any changes in your condition. Remember: Identifying potential complications early can be the key to more effective treatment.
Arthritis
Bone Loss
Eye Disorders
Kidney Disorders
Liver Disease
Skin Disorders
Possible Complications
The complications of Crohn's disease and ulcerative colitis (
collectively known as inflammatory bowel disease, or IBD) are
generally categorized as either local or systemic. The term "local"
refers to a complication involving the intestinal tract itself.
The term "systemic" (or extraintestinal) refers to complications involving
other organs or complications that affect the patient as a whole --
rather than just the bowel.
In uncomplicated IBD, appropriate treatment of inflammation results in
clinical improvement. The patient gets better. When a complication occurs,
however, the improvement is delayed, and a specific treatment may be needed
to target and resolve that complication. It is important for patients and
physicians to be acquainted with these complications because early
recognition often means more effective treatment. Many of the same
complications occur in both Crohn's disease and ulcerative colitis,
and are discussed together. Other complications are specific for ulcerative
colitis or Crohn's disease.
What Are the Systemic (Extraintestinal) Complications of IBD?
Systemic complications -- which include fever, weakness, and loss of appetite
-- are a reflection of the inflammation in the small intestine and/or colon.
But there are also some people with IBD who suffer from certain types of
arthritis, skin conditions, inflammation of the eyes, liver and kidney disorders, and bone loss.
Of all the extraintestinal complications, arthritis is
the most common. Joint, eye, and skin complications often occur together.
For unknown reasons, the extraintestinal or systemic manifestations may
predominate in children and even overshadow the intestinal symptoms,
which may make diagnosis even more difficult. It is, therefore,
important to keep close watch on youngsters who fail to grow or thrive,
feel sick, have fever, and complain of general malaise and weakness.
These may be systemic manifestations of IBD.
On behalf of learning, and use as teaching tools for those of us who need to
know about our disease, I have tried to supply you with as much information as
I could find on all of the drugs, treatments and disorders associated with
Inflammatory Bowel Diseases. I have tried to blend all facts supported by research
and also from personal experiences of other IBD sufferers into one readable webpage, and any and all information presented here is not entirely
from one source. Most information contained within these pages is found in the public domain.
At times you may find information used from another site, and as with all copyrighted materials you may find on these pages, I claim fair use under sections 107 through 118 of the Copyright Act (title 17, U.S. Code). Click here for more info
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