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Complete heart block in a Caucasian woman with Behçet's disease: a case report
Sabeeh-Ur-Rehman Butt1,2, Julian McNeil3
1Department of Medicine, Lyell McEwin Hospital, Elizabeth Vale, SA, 5112, Australia. drsabeehurrehman@yahoo.com.
Insights
Behçet
Area of Science:
- Rheumatology
- Cardiology
- Immunology
Background:
- Behçet's disease is a rare inflammatory vasculitis.
- Cardiac involvement is an uncommon but serious complication.
- Complete heart block is a rare manifestation, particularly in Caucasian populations.
Observation:
- A 48-year-old Caucasian woman presented with symptomatic complete heart block.
- She had a history of recurrent oral/genital ulcers, oligoarthritis, diarrhea, and ocular inflammation.
- Diagnosis of Behçet's disease was confirmed via international study group criteria.
Findings:
- The patient required pacemaker implantation due to complete heart block.
- Treatment with prednisolone and sulfasalazine resulted in a positive response.
- No evidence of cardiac ischemia or abnormal autoimmune antibodies was found.
Implications:
- Highlights the importance of considering cardiac complications in Behçet's disease, irrespective of ethnicity.
- Emphasizes that cardiovascular involvement in Behçet's disease can lead to significant morbidity and mortality.
- Suggests prompt diagnosis and management are crucial for patients with Behçet's disease and cardiac symptoms.
Background:
Behçet's disease is a progressive diffuse inflammatory vasculitis characterized by recurrent oral and genital ulceration and ocular inflammation. Cardiac involvement is a rare but well-documented manifestation of Behçet's disease. Complete heart block in non-Caucasian populations has been reported previously; however, in this report, we describe a unique case of complete heart block in a Caucasian woman with Behçet's disease.
Case Presentation:
A 48-year-old Caucasian woman presented to our hospital with symptomatic complete heart block requiring a pacemaker implant on a background of recurrent oral and genital ulcers and oligoarthritis of 10 months' duration. She also had a history of recurrent diarrhea with a single episode of ocular inflammation in the recent past. She had no evidence of cardiac ischemia, and her autoimmune antibodies were within normal ranges. She was diagnosed with Behçet's disease according to international study group criteria and was commenced on prednisolone and sulfasalazine, to which she responded very well.
Conclusions:
Cardiac complications should be considered when making a diagnosis of Behçet's disease, even in Caucasian patients. While mucocutaneous ulceration is indeed the most common manifestation of Behçet's disease, cardiovascular involvement tends to cause the most morbidity and mortality.
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