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Primary atrophic solitary morphea profunda

Khelifa, Elhem
Masouyé, Isabelle
Chavaz, Pierre
Hauser, Herman
Grillet, Jean-Pierre
Published in Dermatology. 2008, vol. 217, no. 3, p. 207-10
Abstract Solitary morphea profunda (SMP) is a distinct form of localized scleroderma, a cutaneous disorder of unknown origin. Here, we describe a patient presenting with noninflammatory cupuliform depressed plaques, without any significant skin induration, pigmentation or texture change, that appeared on the left shoulder at a site of previous intramuscular vaccination. Light microscopy studies revealed excessive dermal collagen deposition with thickened hyalinized collagen bundles. Magnetic resonance imaging studies demonstrated tissue fibrosis with thinning of the subcutaneous fat tissue and involvement of the adjacent deltoid muscle, which was confirmed by electromyographic tests. Borrelia serology was negative. Our observation of SMP differed from previously described cases, since it mimicked localized lipoatrophy. Our observation highlights the wide spectrum of clinical presentations of localized scleroderma. The latter should be considered in the presence of lipoatrophy-like lesions for proper workup and therapy.
Keywords FemaleHumansMagnetic Resonance ImagingMiddle AgedScleroderma, Localized/pathology
PMID: 18596375
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KHELIFA, Elhem et al. Primary atrophic solitary morphea profunda. In: Dermatology, 2008, vol. 217, n° 3, p. 207-10. https://archive-ouverte.unige.ch/unige:1053

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Deposited on : 2009-03-03

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