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Northeast Florida Medicine

Vol. 66, No. 4 2015

45

Inflammatory Bowel Disease

being used to treat the underlying condition. These include

azathioprine, 5-ASA, Flagyl, and, occasionally, corticoste-

roids. Drug-induced pancreatitis typically resolves rapidly

after discontinuation of the drug. Autoantibodies directed

against pancreatic tissue have been described. There is a

suggestion that inflammation of the duodenum and papil-

la in CD may account for some drainage difficulties and

pancreatitis in these patients as well.

Thromboembolic Events

Venous and arterial thromboembolisms are disease specific

extraintestinal symptoms in patients with IBD that can cause

significant morbidity and mortality. It is thought that there

is a two to fourfold increase of venous thrombosis in patients

with IBD. Arterial embolism is much less frequent. In pa-

tients with IBD, coagulation and fibrinolysis are activated

due to acute and chronic inflammation.When patients with

IBD are in clinical remission, they still remain at risk for

thromboembolic events. Extensive colonic involvement has

been associated with these disorders. Genetic factors includ-

ing hypercoagulability, such as Factor V Leiden, Factor II

mutation, or theMTHFR genemutation, have been studied

in patients with IBD. Increased levels of homocysteine have

been detected in patients with IBD as compared to controls.

In addition, B12 deficiency and folate deficiency may in-

deed aggravate hyperhomocysteinemia. All hospitalized and

immobilized patients with IBD should be treated with low

dose heparin for prophylaxis.

12

Pulmonary Manifestations

Pulmonary manifestations in patients with IBD are rec-

ognized somewhat less frequently than other manifestations.

Several studies have shown empiric pulmonary function

with disturbance in diffusing capacity and up to 50 per-

cent of patients with IBD, even those without respiratory

symptoms.

13

These pulmonary features may include upper

airway disease, large and small airway manifestations, and

parenchymal disease, such as that seen with cryptogenic or-

ganizing pneumonia. One possible link between pulmonary

disease as an extraintestinal manifestation of IBD might be

the common embryologic of the GI and pulmonary epithe-

lium from the primitive foregut. In general, patients with

UC are at a higher risk of developing these manifestations

as compared to those with CD.

The most common pulmonary involvement with these

conditions is bronchiectasis, followed by chronic bronchitis.

Chest radiography is fairly nonspecific, but when high resolu-

tionCT is done, a physician commonly finds dilated airways

and bronchial wall thickening in these affected patients.

Upper airway disease may include subglottic stenosis and a

diffuse tracheitis.The bronchiolitis obliterans withorganizing

pneumonia (BOOP) is the most frequent manifestation of

parenchymal pulmonary disease. These patients have fever,

cough, and dyspnea. Radiographs reveal patchy opacities,

whereas CT will show scattered unilateral or bilateral foci

of consolidation and centrilobular nodules. Methotrexate

is used to treat inflammatory bowel disease, and a hyper-

sensitivity pneumonitis and occasional pulmonary fibrosis

may be seen. In addition, serositis presenting with pleural

effusions, pericarditis, pleural pericarditis or myocarditis can

develop as a result of drug therapy for IBD. Depending on

the type of pulmonary manifestation, any drugs that could

be remotely responsible must be withdrawn immediately.

Typically pulmonary symptoms either induced by the disease

or by its specific treatments, show good response to inhaled

corticosteroids. IV steroids may be necessary as well.

Some less common pulmonary features associated with

IBDcan include a chronic suppurative bronchitis, subglottic

stenosis, necrobiotic nodules within the lung parenchyma,

chronic bronchiolitis, and pulmonary infiltrates with eo-

sinophilia. In addition, it appears that some patients with

concomitant IBD may also have pulmonary sarcoidosis.

Both diseases have an association with HLA A3, B8, DR3.

Parenchymal lung disease in Crohn’s follows the onset of

bowel symptoms with a delay ranging anywhere from1 to 19

years.

13

However, pulmonary symptoms have been reported

to predate the intestinal manifestations of these diseases.

14

WithCrohn’s disease, fistulae can develop anywhere through-

out the GI tract, and these sinus tracts have been noted to

communicate with the airway and parenchyma from the

esophagus, ileum, or colon. This rare phenomenon should

be considered in any patient with active intestinal disease

who has recurrent pneumonia of unclear cause.

Part of the treatment plan for IBD may include mesa-

lamine products or 5-ASA. These compounds are used to

treat both ulcerative colitis and Crohn’s. An increase in

cough and exacerbation of asthma has been noted with

these drugs. Pharyngitis, sinusitis, and chest pain are also

more frequently seen in those taking these medications

compared to placebo. A very rare lymphocytic alveolitis has

been reported with the use of mesalamine. Mesalamine has

also been implicated in both acute and chronic eosinophilic

pneumonia. Infliximab, a monoclonal antibody directed

against anti-tumor necrosis factor alpha, has had a major

impact on the treatment of IBD. It is also used to treat

rheumatoid arthritis, and sarcoidosis. It has a dramatic effect

on granulomatous inflammation. However, it has also been

reported to predispose patients to life threatening infection,

the most widely publicized being reactivation of tuberculo-

sis.

3

Other opportunistic infections have also been reported