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Localized Forms of Scleroderma

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Scleroderma

Abstract

Morphea, also called localized scleroderma, is a fibrosing disorder that resembles scleroderma (systemic sclerosis) microscopically, but typically has a quite different clinical presentation, course and possible pathophysiology. The individual with morphea has single or multiple circumscribed indurated cutaneous plaques that can have variable appearances, depending on the subtype (see classification below and Table 12.1). The main variants are circumscribed or plaque-type morphea (Fig. 12.1a), generalized morphea (Fig. 12.1b), linear morphea (Figs. 12.1c–f and 12.2a–d), and deep morphea or morphea profunda. Unlike scleroderma, systemic disease and involvement of internal organs are uncommon in morphea.

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Acknowledgment

We appreciate the expertise of Geralyn Bodeker, MS AHP in the Palo Alto Medical Foundation Group library and her help with obtaining reference material.

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Correspondence to Amy E. Gilliam MD .

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This chapter is dedicated to James N. Gilliam, MD, a loving husband and father, who inspired our careers and our mutual interests in autoimmunity.

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Gilliam, A.E., Gilliam, A.C. (2012). Localized Forms of Scleroderma. In: Varga, J., Denton, C., Wigley, F. (eds) Scleroderma. Springer, Boston, MA. https://doi.org/10.1007/978-1-4419-5774-0_12

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