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Unilateral generalized morphea: First case report in Taiwan
Meng-Che Lu1,2,3, Shyh-Dar Shyur1,4, Lee-Wen Lee1
1Department of Allergy, Immunology and Rheumatology, Mackay Children's Hospital, Taipei, Taiwan.
Unilateral generalised morphea (UGM), a rare localized scleroderma variant, can affect children. This case report details successful treatment of pediatric UGM using oral medications and topical therapies, avoiding IV pulse therapy.
Area of Science:
- Dermatology
- Paediatric Rheumatology
- Autoimmune Diseases
Background:
- Generalised morphea (GM) is a subtype of localized scleroderma, typically presenting with bilateral skin manifestations.
- Unilateral generalised morphea (UGM) is a rare, asymmetric variant of GM, posing unique clinical challenges.
Observation:
- A case of UGM in a Taiwanese girl affecting the left side of her body, including extremities and trunk.
- Clinical presentation included hyperpigmentation, skin tightness, atrophy, and mild range of motion limitation in the left knee.
Findings:
- The patient received a treatment regimen including oral prednisolone, methotrexate (MTX), and D-penicillamine, alongside topical emollients and glucocorticoids.
- Gradual tapering of oral prednisolone was implemented.
- Significant improvement in all symptoms was observed following the treatment and a consistent rehabilitation program.
Implications:
- This case report offers a potential treatment strategy for pediatric UGM, demonstrating efficacy without requiring intravenous methylprednisolone pulse therapy.
- Highlights the importance of a multidisciplinary approach involving medication and rehabilitation for managing UGM in children.
- Contributes to the limited evidence base for UGM treatment, particularly in the pediatric population.
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