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Regauer, S; Liegl, B; Reich, O; Pickel, H; Beham-Schmid, C.
Vulvar lichen sclerosus. The importance of early clinical and histological diagnosis
Hautarzt. 2004; 55(2):158-164
Doi: 10.1007/s00105-003-0645-8
Web of Science
PubMed
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- Führende Autor*innen der Med Uni Graz
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Regauer Sigrid
- Co-Autor*innen der Med Uni Graz
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Beham-Schmid Christine
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Liegl-Atzwanger Bernadette
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Reich Olaf
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- Abstract:
- Vulvar lichen sclerosus (LS) is a chronic progressive skin disease of unclear etiology. It is often overlooked in early stages, but progresses to destructive atrophy and is associated with an increased risk of vulvar squamous cell carcinoma. The classical symptoms are pruritus and pain, but they are often not distinctive, so that unclear vulvar problems often lead to a biopsy. The histological picture of early LS is quite different from that of late LS with an atrophic epidermis, markedly sclerotic dermis and stiff dilated vessels. The epidermis in early LS is usually normal with only minor irregularities in the rete pattern. The basement membrane is normal or focally widened, while the edematous dermis has only scattered ectatic vessels. The often dense lichenoid and intraepidermal infiltrate explains the spongiosis and vacuolization of the basal layer keratinocytes. Very early cases may only have a sparse lymphocytic infiltrate and hyper-/parakeratosis of the follicular ostia. Early topical therapy can dampen the progression to atrophic, irreversible LS.
- Find related publications in this database (using NLM MeSH Indexing)
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Adult -
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Biopsy -
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Carcinoma, Squamous Cell - etiology
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Child - etiology
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Female - etiology
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Humans - etiology
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Lichen Sclerosus et Atrophicus - complications
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Risk Factors - complications
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Skin - pathology
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Time Factors - pathology
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Vulva - pathology
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Vulvar Diseases - complications
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Vulvar Lichen Sclerosus - etiology
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Vulvar Neoplasms - etiology
- Find related publications in this database (Keywords)
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etiology
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classification
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dermatitis
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lymphocytic infiltrate
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malignant potential of LS