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Published on: June 14, 2016
Papular Mucinosis Associated with Systemic Lupus Erythematosus
Woo Jin Lee1, Gyeong Hun Park1, Sung Eun Chang1
1Department of Dermatology, Asan Medical Center,University of Ulsan College of Medicine, Seoul, Korea.
Papulonodular mucinosis, a rare lupus erythematosus variant, presents as dermal mucin without typical skin inflammation. This case highlights a unique presentation and successful treatment with steroids and antimalarials.
Area of Science:
- Dermatology
- Rheumatology
- Pathology
Background:
- Papulonodular mucinosis (PNM) is a rare variant of lupus erythematosus (LE).
- PNM is histologically defined by diffuse dermal mucin and lacks typical epidermal inflammatory changes.
Observation:
- A 32-year-old man presented with erythematous papules on his lower back, diagnosed as papulonodular mucinosis.
- The patient had systemic lupus erythematosus but no other characteristic LE skin manifestations like malar rash, discoid rash, or photosensitivity for two years.
Findings:
- The case demonstrates a distinct presentation of papulonodular mucinosis in a patient with systemic lupus erythematosus.
- Histological examination revealed diffuse dermal mucin without epidermal inflammation, consistent with PNM.
Implications:
- This case underscores the diverse cutaneous presentations of lupus erythematosus.
- Successful treatment with topical steroids, systemic antimalarials, and steroids led to remission of PNM without recurrence.
- Highlights the importance of considering rare variants in LE diagnosis and management.
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