Selected Publication:
Rompel, R; Mischke, AL; Langner, C; Happle, R.
Linear atrophoderma of Moulin.
Eur J Dermatol. 2000; 10(8):611-613
(- Case Report)
[OPEN ACCESS]
Web of Science
PubMed
- Co-authors Med Uni Graz
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Langner Cord
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- Abstract:
- We report a typical case of linear atrophoderma of Moulin that represents a distinct clinical entity. A 17-year-old woman presented with hyperpigmented and atrophic band-like skin lesions measuring 3-5 cm in breadth on the right side of her trunk and on the right buttock, in an arrangement following the system of Blaschko's lines. The skin lesions had a normal texture and showed no signs of inflammation, lilac ring, erythema, induration, sclerosis or depigmentation. Routine laboratory data were normal. Antinuclear antibodies and anti-Scl70-antibodies were negative. Histopathologically, a moderate diffuse hyperpigmentation within the lower epidermis, a focal vacuolar degeneration of the basal layer, and a few dermal perivascular lymphocytes accompanied by signs of pigment incontinence were noted. Intravenous penicillin G was administered for 14 days in a dosage of 10 x 10(6) IU twice daily. This treatment was repeated after 3 and 9 months. No effect was noted. Linear atrophoderma of Moulin takes a chronic course without progression or regression. The disease leads to significant cosmetic impairment and this may cause emotional stress. Due to its relationship to idiopathic atrophoderma of Pierini-Pasini and linear scleroderma, treatment with intravenous penicillin was tried. In our case it had no effect.
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Adolescent -
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Atrophy - complications
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Biopsy, Needle - complications
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Female - complications
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Humans - complications
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Hyperpigmentation - complications
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Prognosis - complications
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Scleroderma, Localized - complications
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Severity of Illness Index - complications
- Find related publications in this database (Keywords)
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linear atrophoderma of Moulin
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Blaschko's lines
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idiopathic atrophoderma of Pierini-Pasini
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linear scleroderma
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penicillin