Abstract
Dupuytren’s disease has been recognized for approximately four centuries. A thorough knowledge of the palmar fascial complex anatomy is imperative for understanding Dupuytren disease pathology. Its presentation, although seemingly constant, is actually variable, depending on the structures involved. Dorsal skin changes in Dupuytren disease are a source of confusion. These can be either in the form of dorsal Dupuytren’s nodules, which are similar to palmar nodules and pathognomonic of the disease or dorsal cutaneous pads, which are encountered equally in Dupuytren disease and in the normal population. There are also two distinct clinical entities associated with palmar fascial proliferation, classic Dupuytren disease and atypical, so-called non-Dupuytren disease. These two types differ in presentation, etiology, treatment, and prognosis. Authors of future epidemiological and outcome studies should not confuse these two clinical entities.
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Rayan, G.M. (2012). Dupuytren’s Disease: Anatomy, Pathology, and Presentation. In: Eaton, C., Seegenschmiedt, M., Bayat, A., Gabbiani, G., Werker, P., Wach, W. (eds) Dupuytren’s Disease and Related Hyperproliferative Disorders. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-22697-7_1
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