Ruxolitinib as a Targeted Therapy for Arthritis and Alopecia Universalis in a Child with APECED: A Case Report

Background Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a rare monogenic autoimmune disorder caused by mutations in the AIRE gene and is characterized by immune dysregulation with multi-organ involvement. While several case reports in adults have demonstrated the successful use of Janus kinase (JAK) inhibitor in controlling autoimmune complications, its use in the pediatric age group remains poorly documented, particularly in the setting of concomitant rheumatologic and dermatologic manifestations. Case Presentation We report an 11-year-old boy with APECED who initially presented at the age of 3 years with alopecia universalis. At 5 years of age, he developed primary hypoparathyroidism and adrenal insufficiency. In 2020, the diagnosis of APECED was confirmed by genetic testing, which revealed a homozygous frameshift variant in the AIRE gene (c.1193del; p.Pro398Argfs*82). Subsequently, he developed nail pitting and dystrophy, recurrent episodes of oral candidiasis, and bilateral nephrocalcinosis. At 10 years of age, he presented to the pediatric rheumatology clinic with symmetrical arthritis involving both wrists and the right knee, associated with pain and swelling. A clinical diagnosis of arthritis was made, with further investigations pending. He was initiated on ruxolitinib at a dose of 5 mg twice daily, which led to gradual improvement in joint symptoms. After three months, the dose was increased to 10 mg twice daily, resulting in marked clinical improvement of arthritis and noticeable regrowth of scalp hair and eyebrows. Residual bilateral limitation of wrist extension persisted. Methotrexate was subsequently added to further optimize arthritis control. Of note, he had 2 episodes of oral candidiasis since he was started on ruxolitinib, both resolved with oral nystatin. Conclusion This case demonstrates the potential therapeutic benefit and favorable safety profile of ruxolitinib in a pediatric patient with APECED, leading to improvement of both arthritis and alopecia universalis.

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Journal
Journal of Human Immunity
Published
2026-05-01
DOI
https://doi.org/10.70962/cis2026abstract.182
Primary Topic
Adrenal Hormones and Disorders
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article
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article

Ruxolitinib as a Targeted Therapy for Arthritis and Alopecia Universalis in a Child with APECED: A Case Report

Amer Khojah, Abdullah Alsonbul, Sattam Almutairi, Aisha Mirza et al.
Journal of Human Immunity
Adrenal Hormones and Disorders
article

Ruxolitinib as a Targeted Therapy for Arthritis and Alopecia Universalis in a Child with APECED: A Case Report

Amer Khojah, Abdullah Alsonbul, Sattam Almutairi, Aisha Mirza, Michail Lionakis
article en

Abstract

Background Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a rare monogenic autoimmune disorder caused by mutations in the AIRE gene and is characterized by immune dysregulation with multi-organ involvement. While several case reports in adults have demonstrated the successful use of Janus kinase (JAK) inhibitor in controlling autoimmune complications, its use in the pediatric age group remains poorly documented, particularly in the setting of concomitant rheumatologic and dermatologic manifestations. Case Presentation We report an 11-year-old boy with APECED who initially presented at the age of 3 years with alopecia universalis. At 5 years of age, he developed primary hypoparathyroidism and adrenal insufficiency. In 2020, the diagnosis of APECED was confirmed by genetic testing, which revealed a homozygous frameshift variant in the AIRE gene (c.1193del; p.Pro398Argfs*82). Subsequently, he developed nail pitting and dystrophy, recurrent episodes of oral candidiasis, and bilateral nephrocalcinosis. At 10 years of age, he presented to the pediatric rheumatology clinic with symmetrical arthritis involving both wrists and the right knee, associated with pain and swelling. A clinical diagnosis of arthritis was made, with further investigations pending. He was initiated on ruxolitinib at a dose of 5 mg twice daily, which led to gradual improvement in joint symptoms. After three months, the dose was increased to 10 mg twice daily, resulting in marked clinical improvement of arthritis and noticeable regrowth of scalp hair and eyebrows. Residual bilateral limitation of wrist extension persisted. Methotrexate was subsequently added to further optimize arthritis control. Of note, he had 2 episodes of oral candidiasis since he was started on ruxolitinib, both resolved with oral nystatin. Conclusion This case demonstrates the potential therapeutic benefit and favorable safety profile of ruxolitinib in a pediatric patient with APECED, leading to improvement of both arthritis and alopecia universalis.

Journal of Human ImmunityVol. 2(CIS2026)
Umm al-Qura University (SA), King Faisal Specialist Hospital & Research Centre (SA), Maternity and Children's Hospital (SA), National Institute of Allergy and Infectious Diseases (US)
Good health and well-being
Openalex Percentile: Top 11%
Adrenal Hormones and Disorders
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