AI Article Synopsis
- A 42-year-old woman experienced both granuloma annulare, appearing as papules and plaques on her feet and abdomen, and morphea characterized by skin fibrosis on her lower limbs.
- The report discusses the possible reasons behind the rare occurrence of these two skin conditions happening together.
- There are very few documented cases of morphea and granuloma annulare coexisting, making this case noteworthy.
Article Abstract
Context: Localized scleroderma (morphea) is characterized by fibrosis of skin and subcutaneous tissue. Granuloma annulare is a relatively common disease that is characterized by dermal papules and arciform plaques.
Case Report: Here, we present the case of a 42-year-old woman who developed granuloma annulare on the dorsum of her feet and abdominal region, and morphea on the anterior side of her lower limbs. We also discuss the etiological and pathogenetic processes that may cause the rare coexistence of these two diseases.
Conclusion: Only a few cases in the literature have described coexistence of morphea and granuloma annulare.
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|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9721217 | PMC |
| http://dx.doi.org/10.1590/1516-3180.2017.0091060617 | DOI Listing |
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Article Synopsis
- Granuloma annulare (GA) is a non-infectious skin condition that can become widespread in some patients; this study focused on those with disseminated GA in a German hospital.
- A total of 239 patients were studied, with 33 having confirmed disseminated GA, predominantly affecting women around the age of 57, and many reporting little to no symptoms.
- Treatment options included glucocorticoids and phototherapy, but only a small percentage achieved remission, highlighting the need for more effective clinical trials for new therapies.
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