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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8005440 | PMC |
| http://dx.doi.org/10.1002/art.41629 | DOI Listing |
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Wong-Type Dermatomyositis: Literature Review of a Rare Variant.
J Clin Rheumatol
October 2024
Department of Internal Medicine, University of Central Florida College of Medicine, Orlando, FL.
Article Synopsis
- - Wong-type dermatomyositis (WTDM) is a rare variant of dermatomyositis first identified in 1969, combining features of classic dermatomyositis and pityriasis rubra pilaris, but has limited documentation due to its rarity and possible clinical oversight.
- - A review of existing literature suggests that WTDM behaves more like a subtype of classic dermatomyositis rather than just a combination of symptoms from both conditions, indicating a better treatment response with traditional DM therapies.
- - Clinicians are advised to conduct thorough evaluations for WTDM patients, including detailed medical histories, exams, and lab tests, and to monitor for systemic issues or cancer, while further research is needed to explore its underlying mechanisms and long
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