Behcet Disease: Difference between revisions

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== Prevalence  ==
== Prevalence  ==
[[Image:Silkroad.jpg|frame|Route of Silk Road]]
Occurs in people among the " Silk Road"- in the eastern Mediterranean, Middle East,and East Asia. Most common in males along the Silk Road countries and more common in females in Europe and the U.S. aged 25-30 years.<ref name="3.">Arthritis Foundation. Behcet's disease: how is it diagnosed? http://www.arthritis.org (accessed February 22 2011).</ref>
*Estimated 15,000 in U.S. with Behcet's.


Occurs in people among the " Silk Road"- in the eastern Mediterranean, Middle East,and East Asia. Most common in males along the Silk Road countries and more common in females in Europe and the U.S. aged 25-30 years.&nbsp;&nbsp;<ref name="3.">Arthritis Foundation. Behcet's disease: how is it diagnosed? http://www.arthritis.org (accessed February 22 2011).</ref> [[Image:Silkroad.jpg|frame|Route of Silk Road]]


*Estimated 15,000 in U.S. with Behcet's.


== Characteristics/Clinical Presentation  ==
== Pathological Process ==
The etiology is unknown but thought to be secondary to an autoimmune reaction, where the immune system attacks and harms the body's tissues, resulting in inflammation. Some thoughts are that it could have a genetic component making some more susceptible to a possible environmental trigger such as a virus or bacterium.&nbsp;&nbsp;<ref name="3." />
== Clinical Presentation  ==
[[Image:Img0019.jpg|frame|Mouth Ulcers]]


The patient could present with any of the five most common symptoms of Behcet's disease.  
The patient could present with any of the five most common symptoms of Behcet's disease.  


*Mouth sores- usually the first and most persistent symptom. &nbsp;They are similar to canker sores but have a longer duration and are usually larger and more painful.  
*Mouth sores- usually the first and most persistent symptom. &nbsp;They are similar to canker sores but have a longer duration and are usually larger and more painful.  
*Genital sores- &nbsp;less common, but still occur in more than half of the patients with this disease. &nbsp;They are usually mistaken as genital herpes and can be on the external or internal surface of the genitalia. &nbsp;  
*Genital sores- &nbsp;less common, but still occur in more than half of the patients with this disease. &nbsp;They are usually mistaken as genital herpes and can be on the external or internal surface of the genitalia. &nbsp;                                                             [[Image:Behcet's_D.JPG|frame|right|Skin lesion on Scrotum]]
*Skin lesions- are red, raised bumps or bruises that resemble boils or acne. &nbsp;They usually appear on the legs and upper torso.&nbsp;  
*Skin lesions- are red, raised bumps or bruises that resemble boils or acne. &nbsp;They usually appear on the legs and upper torso.&nbsp;  
*Uvelitis and retinal vasculitis- occuring in half the Behcet's patients, this can cause blurred vision, pain, redness, or blindness if left untreated.&nbsp;  
*Uvelitis and retinal vasculitis- occuring in half the Behcet's patients, this can cause blurred vision, pain, redness, or blindness if left untreated.&nbsp;  
Line 38: Line 44:
*Digestive tract- may lead to abdominal pain, diarrhea, and bleeding due to inflammation and ulcers in GI tract. These symptoms are similar to ulcerative colitis and Crohn's disease.&nbsp;<ref name="3." />
*Digestive tract- may lead to abdominal pain, diarrhea, and bleeding due to inflammation and ulcers in GI tract. These symptoms are similar to ulcerative colitis and Crohn's disease.&nbsp;<ref name="3." />


== Associated Co-morbidities   ==
=== Associated Co-morbidities ===


Include: ulcerations in mouth, genitals, and GI tract, skin lesions, lung aneurysms, arthralgias, headaches, confusion, strokes, personality changes, dementia, and aseptic meningitis, anterior/posterior uveitis&nbsp;<ref name="4.">The John Hopkins Vasculitis Center. Hellmann D. Behcet's disease. www.hopkinsvasculitis.org (accessed 22 February 2011).</ref> [[Image:Img0019.jpg|frame|Mouth Ulcers]]


== Medications  ==
Include: ulcerations in mouth, genitals, and GI tract, skin lesions, lung aneurysms, arthralgias, headaches, confusion, strokes, personality changes, dementia, and aseptic meningitis, anterior/posterior uveitis&nbsp;<ref name="4.">The John Hopkins Vasculitis Center. Hellmann D. Behcet's disease. www.hopkinsvasculitis.org (accessed 22 February 2011).</ref>


For the disease that's confined to the mucocutaneous areas (mouth, genitals, skin) use topical steroids and non immunosuppressive medications.&nbsp;
=== Systemic Involvement ===
[[Image:GI.jpeg|frame|Ulcers in GI tract]]


Moderate dosage of corticosteroids are used for exacerbations.  For some patients with chronic pain, low doses of prednisone are indicated.&nbsp;Serious organ involvement calls for high doses of Prednisone and immunosuppressive treatment.  Immunosuppressive medications include: azathrioprine, cyclosporine, cyclophosphamide, and chlorambucil&nbsp;<ref name="4." />
Can affect the eyes, mouth, skin, lungs, joints, brain, genitals, and GI tract.  


== Diagnostic Tests/Lab Tests/Lab Values  ==
*Eyes: May cause anterior/ posterior uveitis; anterior uveitis results in pain, blurry vision, tearing, redness, and light sensitivity; posterior uveitis causes fewer symptoms but damages the retina.
 
*Mouth: Painful sores called aphthous ulcers can be found on the lips, tongue, and inside of the cheek.
Diagnosis is very difficult and may takes months or even years to get an accurate diagnosis. Key symptoms are: [[Image:Behcet's_D.JPG|frame|right|Skin lesion on Scrotum]]
*Skin: Erythema nodosum which are red, tender nodules that can occur on the legs and ankles commonly, but also on the face, neck, and arms or pustular skin lesions which resemble acne.&nbsp;
 
*Lungs: Aneurysms in arteries of lungs--&gt; which can lead to  hemorrhage.&nbsp;
*Mouth sores at least three times in one year.  
*Joints: Arthralgias
*Any two of the following:  
*Brain: Headaches, confusion, strokes, personality changes, dementia, and aseptic meningitis.
*Recurring genital sores
*Genitals: painful lesions that form on the scrotum or vulva.
*Eye inflammation with loss of vision
*Gastrointestional: Ulcerations that occur from the mouth to the anus. The most common sites are the ileum and cecum.&nbsp;<ref name="4." />
*Characteristic skin lesions  
== Diagnostic Procedures  ==
*Positive pathergy test
[[Image:Lungs.jpg|frame|Behcet's affecting the lungs]]


<br>
Diagnosis is very difficult and may takes months or even years to get an accurate diagnosis. Key symptoms are:
*Mouth sores at least three times in one year.
*Any two of the following:
*Recurring genital sores
*Eye inflammation with loss of vision
*Characteristic skin lesions
*Positive pathergy test<br>[[Image:Neuro.jpg|frame|MRI of CNS involvement (white matter changes in the pons)]]


A dermatologist may do a biopsy of the mouth, genitals, and skin lesions.&nbsp;<ref name="3." />&nbsp;
A dermatologist may do a biopsy of the mouth, genitals, and skin lesions.&nbsp;<ref name="3." />&nbsp;
== Etiology/Causes  ==
The etiology is unknown but thought to be secondary to an autoimmune reaction, where the immune system attacks and harms the body's tissues, resulting in inflammation. Some thoughts are that it could have a genetic component making some more susceptible to a possible environmental trigger such as a virus or bacterium.&nbsp;&nbsp;<ref name="3." />
[[Image:Lungs.jpg|frame|Behcet's affecting the lungs]]
[[Image:GI.jpeg|frame|Ulcers in GI tract]]


== Systemic Involvement  ==


Can affect the eyes, mouth, skin, lungs, joints, brain, genitals, and GI tract.&nbsp;


*Eyes: May cause anterior/ posterior uveitis; anterior uveitis results in pain, blurry vision, tearing, redness, and light sensitivity; posterior uveitis causes fewer symptoms but damages the retina.
*Mouth: Painful sores called aphthous ulcers can be found on the lips, tongue, and inside of the cheek.
*Skin: Erythema nodosum which are red, tender nodules that can occur on the legs and ankles commonly, but also on the face, neck, and arms or pustular skin lesions which resemble acne.&nbsp;
*Lungs: Aneurysms in arteries of lungs--&gt; which can lead to hemorrhage.&nbsp;
*Joints: Arthralgias
*Brain: Headaches, confusion, strokes, personality changes, dementia, and aseptic meningitis. [[Image:Neuro.jpg|frame|MRI of CNS involvement (white matter changes in the pons)]]
*Genitals: painful lesions that form on the scrotum or vulva.
*Gastrointestional: Ulcerations that occur from the mouth to the anus. The most common sites are the ileum and cecum.&nbsp;<ref name="4." />


== Medical Management ==
== Management / Interventions ==


=== Medical Management ===
Steroid gels, pastes, and creams can be used for mouth and genital ulcers. Colchicine helps to reduce recurrent ulcers. Pentoxifylline can be used to maintain the healed ulcers for up to 29 months. Ibuprofen can be used to decrease joint inflammation. Colchicine and cortisone are used for inflammation in patients. Sulfasalazine is used to decrease the symptoms for arthritis. Immediate attention has to be given to treat the eyes and reduce inflammation. Research has indicated that by blocking TNF, a protein that initiates inflammation, physicians can successfully manage inflammation. TNF blocking medications include infliximab and etanercept. Immunosuppressive drugs have been used to treat the more severe symptoms associated with the brain, eyes, and arteries. The immunosuppressive agents include: chlorambucil, azathioprine, and cyclophosphamide. Current literature is looking at the effects of thalidomide for treating and preventing ulcerations in the mouth and genitals.&nbsp;<ref name="5.">MedicineNet.com. Behcet's syndrome. http://www.medicinenet.com (accessed March 15 2011).</ref>  
Steroid gels, pastes, and creams can be used for mouth and genital ulcers. Colchicine helps to reduce recurrent ulcers. Pentoxifylline can be used to maintain the healed ulcers for up to 29 months. Ibuprofen can be used to decrease joint inflammation. Colchicine and cortisone are used for inflammation in patients. Sulfasalazine is used to decrease the symptoms for arthritis. Immediate attention has to be given to treat the eyes and reduce inflammation. Research has indicated that by blocking TNF, a protein that initiates inflammation, physicians can successfully manage inflammation. TNF blocking medications include infliximab and etanercept. Immunosuppressive drugs have been used to treat the more severe symptoms associated with the brain, eyes, and arteries. The immunosuppressive agents include: chlorambucil, azathioprine, and cyclophosphamide. Current literature is looking at the effects of thalidomide for treating and preventing ulcerations in the mouth and genitals.&nbsp;<ref name="5.">MedicineNet.com. Behcet's syndrome. http://www.medicinenet.com (accessed March 15 2011).</ref>  


Research indicates that the prognosis is variable and depending on the severity and where the symptoms occur, some will diminish over time. Usually symptoms of the CNS will not diminish, however.
Research indicates that the prognosis is variable and depending on the severity and where the symptoms occur, some will diminish over time. Usually symptoms of the CNS will not diminish, however.


== Physical Therapy Management ==
==== Medications ====
For the disease that's confined to the mucocutaneous areas (mouth, genitals, skin) use topical steroids and non immunosuppressive medications.&nbsp;
 
Moderate dosage of corticosteroids are used for exacerbations.  For some patients with chronic pain, low doses of prednisone are indicated.&nbsp;Serious organ involvement calls for high doses of Prednisone and immunosuppressive treatment. Immunosuppressive medications include: azathrioprine, cyclosporine, cyclophosphamide, and chlorambucil&nbsp;<ref name="4." />


=== Physical Therapy Management ===
Energy conservation techniques, low-moderate intensity exercise endurance and strengthening, ROM, education on disease process, relaxation techniques, modalities for pain control
Energy conservation techniques, low-moderate intensity exercise endurance and strengthening, ROM, education on disease process, relaxation techniques, modalities for pain control


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== '''Case Studies'''  ==
== '''Case Studies'''  ==


*&nbsp;Regional distinction for the clinical severity of Behcet's disease in Korea: four university-based medical centre studies. <ref name="9.">Choe JY, Chung WT, Lee SW, et al. Regional distinction for the clinical severity of Behcet’s disease in Korea: four university-based medical centre studies. Clinical and experimental rheumatology. 2010;28:S20-S26.</ref>[view article in Clinical and Experimental Rheumatology, 2010] <br>
*Regional distinction for the clinical severity of Behcet's disease in Korea: four university-based medical centre studies. <ref name="9.">Choe JY, Chung WT, Lee SW, et al. Regional distinction for the clinical severity of Behcet’s disease in Korea: four university-based medical centre studies. Clinical and experimental rheumatology. 2010;28:S20-S26.</ref>[view article in Clinical and Experimental Rheumatology, 2010] <br>
*Clinical manifestations of Behcet's disease: an analysis of 2147 patients<ref name="10.">Gurler A, Boyvat A, Tursen U. Clinical manifestations of Behcet’s disease: an analysis of 2147 patients. Yonsei Medical Journal. 1997; 38:423-427.</ref> [view article in Yonsei Medical Journal]  
*Clinical manifestations of Behcet's disease: an analysis of 2147 patients<ref name="10.">Gurler A, Boyvat A, Tursen U. Clinical manifestations of Behcet’s disease: an analysis of 2147 patients. Yonsei Medical Journal. 1997; 38:423-427.</ref> [view article in Yonsei Medical Journal]  
*Clinical patterns of neurological involvement in Behçet's disease: evaluation of 200 patients <ref name="12.">Akman-Demir G, Serdaroglu P, Tasci B. Clinical patterns of neurological involvement in Behçet's disease: evaluation of 200 patients. Oxford Journals. 1999;122:2171-2182.</ref>&nbsp;[ view article in Oxford Journal]<br>
*Clinical patterns of neurological involvement in Behçet's disease: evaluation of 200 patients <ref name="12.">Akman-Demir G, Serdaroglu P, Tasci B. Clinical patterns of neurological involvement in Behçet's disease: evaluation of 200 patients. Oxford Journals. 1999;122:2171-2182.</ref>&nbsp;[ view article in Oxford Journal]<br>

Revision as of 21:23, 5 September 2023

This article is currently under review and may not be up to date. Please come back soon to see the finished work! (05/09/2023)

Definition/Description[edit | edit source]

A syndrome (or sometimes referred to as a disease) that causes inflammation in the blood vessels of the body. The most common symptoms are sores in the mouth, sex organs, and on the skin, as well as swelling in the eye, pain, stiffness, and swelling in the joints. The more serious complications include meningitis, blood clots, inflammation of the gastrointestinal (GI) tract, and blindness. [1][2] 

[3]

Prevalence[edit | edit source]

Route of Silk Road

Occurs in people among the " Silk Road"- in the eastern Mediterranean, Middle East,and East Asia. Most common in males along the Silk Road countries and more common in females in Europe and the U.S. aged 25-30 years.[4]

  • Estimated 15,000 in U.S. with Behcet's.



Pathological Process[edit | edit source]

The etiology is unknown but thought to be secondary to an autoimmune reaction, where the immune system attacks and harms the body's tissues, resulting in inflammation. Some thoughts are that it could have a genetic component making some more susceptible to a possible environmental trigger such as a virus or bacterium.  [4]

Clinical Presentation[edit | edit source]

File:Img0019.jpg
Mouth Ulcers

The patient could present with any of the five most common symptoms of Behcet's disease.

  • Mouth sores- usually the first and most persistent symptom.  They are similar to canker sores but have a longer duration and are usually larger and more painful.
  • Genital sores-  less common, but still occur in more than half of the patients with this disease.  They are usually mistaken as genital herpes and can be on the external or internal surface of the genitalia.  
    File:Behcet's D.JPG
    Skin lesion on Scrotum
  • Skin lesions- are red, raised bumps or bruises that resemble boils or acne.  They usually appear on the legs and upper torso. 
  • Uvelitis and retinal vasculitis- occuring in half the Behcet's patients, this can cause blurred vision, pain, redness, or blindness if left untreated. 
  • Arthritis- it results in inflammation in the joints leading to edema, heat, redness, and pain. It occurs in half the Behcet's patients and lasts a few weeks.

In addition to these five common clinical symptoms that patients present with, the circulatory, central nervous systems, and digestive tract can be affected. 

  • Circulatory system- DVT, aneurysms
  • Central nervous system- may experience fever, headache, stiff neck, and difficulty coordinating movements secondary to inflammation in the meninges in the brain and spinal cord. 
  • Digestive tract- may lead to abdominal pain, diarrhea, and bleeding due to inflammation and ulcers in GI tract. These symptoms are similar to ulcerative colitis and Crohn's disease. [4]

Associated Co-morbidities[edit | edit source]

Include: ulcerations in mouth, genitals, and GI tract, skin lesions, lung aneurysms, arthralgias, headaches, confusion, strokes, personality changes, dementia, and aseptic meningitis, anterior/posterior uveitis [5]

Systemic Involvement[edit | edit source]

File:GI.jpeg
Ulcers in GI tract

Can affect the eyes, mouth, skin, lungs, joints, brain, genitals, and GI tract.

  • Eyes: May cause anterior/ posterior uveitis; anterior uveitis results in pain, blurry vision, tearing, redness, and light sensitivity; posterior uveitis causes fewer symptoms but damages the retina.
  • Mouth: Painful sores called aphthous ulcers can be found on the lips, tongue, and inside of the cheek.
  • Skin: Erythema nodosum which are red, tender nodules that can occur on the legs and ankles commonly, but also on the face, neck, and arms or pustular skin lesions which resemble acne. 
  • Lungs: Aneurysms in arteries of lungs--> which can lead to hemorrhage. 
  • Joints: Arthralgias
  • Brain: Headaches, confusion, strokes, personality changes, dementia, and aseptic meningitis.
  • Genitals: painful lesions that form on the scrotum or vulva.
  • Gastrointestional: Ulcerations that occur from the mouth to the anus. The most common sites are the ileum and cecum. [5]

Diagnostic Procedures[edit | edit source]

File:Lungs.jpg
Behcet's affecting the lungs

Diagnosis is very difficult and may takes months or even years to get an accurate diagnosis. Key symptoms are:

  • Mouth sores at least three times in one year.
  • Any two of the following:
  • Recurring genital sores
  • Eye inflammation with loss of vision
  • Characteristic skin lesions
  • Positive pathergy test
    MRI of CNS involvement (white matter changes in the pons)

A dermatologist may do a biopsy of the mouth, genitals, and skin lesions. [4] 



Management / Interventions[edit | edit source]

Medical Management[edit | edit source]

Steroid gels, pastes, and creams can be used for mouth and genital ulcers. Colchicine helps to reduce recurrent ulcers. Pentoxifylline can be used to maintain the healed ulcers for up to 29 months. Ibuprofen can be used to decrease joint inflammation. Colchicine and cortisone are used for inflammation in patients. Sulfasalazine is used to decrease the symptoms for arthritis. Immediate attention has to be given to treat the eyes and reduce inflammation. Research has indicated that by blocking TNF, a protein that initiates inflammation, physicians can successfully manage inflammation. TNF blocking medications include infliximab and etanercept. Immunosuppressive drugs have been used to treat the more severe symptoms associated with the brain, eyes, and arteries. The immunosuppressive agents include: chlorambucil, azathioprine, and cyclophosphamide. Current literature is looking at the effects of thalidomide for treating and preventing ulcerations in the mouth and genitals. [6]

Research indicates that the prognosis is variable and depending on the severity and where the symptoms occur, some will diminish over time. Usually symptoms of the CNS will not diminish, however.

Medications[edit | edit source]

For the disease that's confined to the mucocutaneous areas (mouth, genitals, skin) use topical steroids and non immunosuppressive medications. 

Moderate dosage of corticosteroids are used for exacerbations. For some patients with chronic pain, low doses of prednisone are indicated. Serious organ involvement calls for high doses of Prednisone and immunosuppressive treatment. Immunosuppressive medications include: azathrioprine, cyclosporine, cyclophosphamide, and chlorambucil [5]

Physical Therapy Management[edit | edit source]

Energy conservation techniques, low-moderate intensity exercise endurance and strengthening, ROM, education on disease process, relaxation techniques, modalities for pain control

Differential Diagnosis[edit | edit source]

Behcet's is rare in the U.S. Many times it is misdiagnosed for other conditions based on the symptoms.

File:Skin.JPG
Skin lesions on forearm

If lesions appear on the mouth, skin, or genitals, it can be mistaken for:

  • Cold sores
  • Canker sores
  • Genital Herpes
  • Herpes
  • Ache

If lesions appear in the GI tract, these are possible incorrect diagnosis:

Other possible diagnosis:

  • Chancroid 
  • Chronic Fatigue Syndrome
  • Encephalitis
  • Granuloma inguinale
  • Mosquito-borne diseases
  • Multiple Sclerosis
  • Oral Ulcer
  • Superficial thrombophlebitis
  • Vulvar cancer
  • Vulvar lesions[7]

Case Studies[edit | edit source]

  • Regional distinction for the clinical severity of Behcet's disease in Korea: four university-based medical centre studies. [8][view article in Clinical and Experimental Rheumatology, 2010]
  • Clinical manifestations of Behcet's disease: an analysis of 2147 patients[9] [view article in Yonsei Medical Journal]
  • Clinical patterns of neurological involvement in Behçet's disease: evaluation of 200 patients [10] [ view article in Oxford Journal]
  • Clinical studies on Behcet's syndrome. [10] [view article at European Journal of Cardiothoracic Surgery]

Resources[edit | edit source]

References[edit | edit source]

  1. National Institute of Arthritis and Musculoskeletal and Skin Diseases. Behcet's disease. http://www.niams.nih.gov (accessed 22 February 2011).
  2. Medline Plus. Behcet's syndrome. http://www.nlm.nih.gov (accessed 22 February 2011).
  3. Bechet's Disease Explained. Available from http://www.youtube.com/watch?v=Txf7cWW8HwI [accessed 28/98/19]
  4. 4.0 4.1 4.2 4.3 Arthritis Foundation. Behcet's disease: how is it diagnosed? http://www.arthritis.org (accessed February 22 2011).
  5. 5.0 5.1 5.2 The John Hopkins Vasculitis Center. Hellmann D. Behcet's disease. www.hopkinsvasculitis.org (accessed 22 February 2011).
  6. MedicineNet.com. Behcet's syndrome. http://www.medicinenet.com (accessed March 15 2011).
  7. WD. Misdiagnosis of behcet’s disease. www.wrongdiagnosis.com. (accessed 31 March 2011).
  8. Choe JY, Chung WT, Lee SW, et al. Regional distinction for the clinical severity of Behcet’s disease in Korea: four university-based medical centre studies. Clinical and experimental rheumatology. 2010;28:S20-S26.
  9. Gurler A, Boyvat A, Tursen U. Clinical manifestations of Behcet’s disease: an analysis of 2147 patients. Yonsei Medical Journal. 1997; 38:423-427.
  10. 10.0 10.1 Akman-Demir G, Serdaroglu P, Tasci B. Clinical patterns of neurological involvement in Behçet's disease: evaluation of 200 patients. Oxford Journals. 1999;122:2171-2182.