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Adult-Onset PFAPA Syndrome: Successful Management with Colchicine
Amulya Balagani1, Farina Tariq2, Muhammad Zaheer1
1Division of Rheumatology, Saint Louis University School of Medicine, Saint Louis, MO, USA.
Insights
Periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome, typically seen in children, can occur in adults. This case shows colchicine effectively reduced flare frequency in adult-onset PFAPA.
Area of Science:
- Rheumatology
- Pediatrics
- Internal Medicine
Background:
- Periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome is a rare autoinflammatory disorder typically affecting young children.
- Its etiology remains unknown, and diagnosis relies on clinical presentation due to the absence of specific biomarkers.
Observation:
- A 22-year-old woman presented with recurrent fevers, sore throat, and cervical adenitis, fulfilling PFAPA criteria.
- Initial investigations for infectious and autoimmune diseases were negative, leading to a clinical diagnosis of PFAPA.
Findings:
- The patient responded well to initial steroid treatment for her PFAPA symptoms.
- Transitioning to oral colchicine significantly decreased the frequency of her recurrent febrile episodes.
Implications:
- This case underscores the importance of considering adult-onset PFAPA in the differential diagnosis of periodic febrile illnesses.
- Awareness and timely diagnosis of PFAPA in adults can improve patient quality of life, with colchicine showing prophylactic potential.
Abstract:
BACKGROUND Periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome is an autoinflammatory fever syndrome primarily seen in children under age 5 years, and its etiology is unknown. Most cases are resolved by the age of 10 years, and it is rare in adults. PFAPA is characterized by recurrent episodes of fever associated with pharyngitis, stomatitis, and cervical adenitis, although not all clinical features are present at initial evaluation. Diagnosis is made clinically, as there are no specific biomarkers available. Treatment includes prednisone, colchicine, interleukin-1 blockers, and tonsillectomy. We report a case of adult-onset PFAPA syndrome that responded to colchicine. CASE REPORT A 22-year-old woman presented to the Rheumatology Clinic for evaluation of recurrent fevers associated with sore throat and enlarged painful cervical lymph nodes. She was symptom-free between the episodes. Workup for infectious causes and autoinflammatory/autoimmune diseases was unremarkable. Various differential diagnoses were considered, due to her unusual presentation. After all were ruled out, PFAPA was diagnosed based on her symptoms, and she started steroids, to which she had a dramatic response and resolution of symptoms. She was then transitioned to oral colchicine, which significantly decreased flare frequency. CONCLUSIONS Being aware of PFAPA syndrome in adults is vital. A timely diagnosis can significantly improve a patient's quality of life. This case highlights the importance of considering PFAPA syndrome in the differential diagnosis of periodic febrile illnesses in adults and the role of Colchicine as prophylaxis. Larger studies are needed to understand etiopathogenesis better and develop other effective therapeutics.
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