Erythemato-Papulo-Squamous Diseases

Braun‐Falco, Otto; Plewig, Gerd; Wolff, Helmut H.; Burgdorf, Walter H. C.

doi:10.1007/978-3-642-97931-6_14

Cited by 16 publications

(15 citation statements)

References 303 publications

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“…Deri kıvrımlarını tutmayan kaldı-rım taşı görünümünde eritemli papüllerle karakterizedir (14). Oluşturduğu bu özel görünüme şezlong belirtisi (deck-chair sign) adı verilir (15,16).…”

Section: Discussionunclassified

Papuloerythroderma of Ofuji: A Report of Two Cases

Sarıcı¹,

Koca²,

Işık³

et al. 2011

Turk J Dermatol

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ÖzetOfuji'nin papuloeritroderması, deri kıvrımlarını tutmayan eritemli yassı papüllerin görüldüğü, yaygın kaşıntılı erüpsiyonla karakterize bir hastalıktır. Sıklıkla yaşlı erkeklerde görülen hastalığa, lenfadenopati, periferik kanda eozinofili, lenfopeni ve IgE yüksekliği eşlik edebilir. T ve B hücreli lenfoma, internal malignensiler, AIDS, atopik dermatit, psoriasis, ilaç hipersensitivitesi ile ilişkisi rapor edilmiştir. Bu nadir hastalığın tedavisinde topikal ve sistemik kortikosteroidler, psoralen-UVA, etretinat-PUVA, asitretin-PUVA, UVB, siklosporin, interferon α ve azatioprin kullanılmaktadır. Bu yazıda Ofuji'nin papuloeritroderması tanısı koyduğumuz 2 olguyu sunmaktayız. ( AbstractPapuloerythroderma of Ofuji is characterized by a pruritic eruption of widespread, red, flat papules that leads to spare skin folds. The disease occurs primarily in elderly men and is often associated with lymphadenopathy, peripheral blood eosinophilia, lymphopenia and elevated immunoglobulin E levels. Association with T and B cell lymphomas, visceral carcinomas, AIDS, atopic dermatitis, psoriasis and hypersensitivity to drugs have been reported. Topical and systemic corticosteroids, psoralen-UVA, etretinate-PUVA, acitretin-PUVA, UVB, cyclosporin, interferon α and azathioprine have been used in the treatment of this rare disease. In this manuscript, we described two patients with papuloerythroderma of Ofuji. (Turk J Dermatol 2011; 5: 13-7)

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Section: Discussionunclassified

Papuloerythroderma of Ofuji: A Report of Two Cases

Sarıcı¹,

Koca²,

Işık³

et al. 2011

Turk J Dermatol

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“…Palmoplantar lichen planus is a rare, 1ocalized variant of the disease and may create difficulty in diagnosis if it is present as an isolated finding (1, 2). Several morphological patterns of palmoplantar lesions in lichen planus have been described including erythematous plaques, punctate keratosis, diffuse keratoderma, and ulcerated lesions (3–6, 9, 10).…”

Section: Discussionmentioning

confidence: 99%

Palmoplantar Lichen Planus Presenting with Vesicle‐Like Papules

Gündüz

İnanır

Türkdoğan

et al. 2003

The Journal of Dermatology

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Palmoplantar lichen planus is a rare, localized variant of the disease that may create difficulty in diagnosis if it is present as an isolated finding. Although several morphological patterns may be seen, plaques or small papules with compact hyperkeratosis are usually observed. We present a 25-year-old woman with a one-month history of slightly pruritic, red papules on her palms and soles. Dermatologic examination revealed numerous, asymptomatic, unscaly, red papules on her palms and soles, some of them resembling vesicles and white reticulate plaques on both sides of the buccal mucosa. The diagnosis was established by the typical histopathological features of lichen planus. Although resistant to topical corticosteroids, she responded well to systemic corticosteroid therapy, and no recurrence was observed during the follow-up period of one year.

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“…Protein loss in the form of desquamation and exudation is significant, resulting in hypoproteinemia. The daily loss of scales increases from 500-1000 mg to 20-30 g (1,14). Typically, there is hypoalbuminemia with a relative increase in immunoglobulins, especially γ-globulins.…”

Section: Pathogenesismentioning

confidence: 99%

“…Erythroderma refers to the skin that is diffusely red and inflamed with varying degrees and types of scaling (1). There are many causes of erythroderma, but the most common are exacerbations of an underlying skin disease, drug reactions and malignancies, primarily mycosis fungoides (MF).…”

Section: Introductionmentioning

confidence: 99%

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Exfoliative Erythroderma

NEUHOLD¹,

WOLFRAM²

Encyclopedia of Cancer

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SUMMARY Exfoliative erythroderma refers to the skin that is diffusely red and inflamed with varying degrees and types of scaling. There are many causes of erythroderma, but the most common are exacerbations of an underlying skin disease, drug reactions and underlying malignancies. Erythroderma is a rare, potentially serious skin condition. Protein loss in the form of desquamation and exudation is significant, resulting in hypoproteinemia. Usually more than one skin biopsy should be done. Biopsy analysis is important to rule out cutaneous T-cell lymphoma. Patients should be carefully evaluated for underlying disease. Erythroderma can represent a serious medical threat to the patient, and may require hospitalization. Various forms of exfoliative erythroderma are presented, considering the etiopathogenesis, physical findings, differential diagnosis and treatment.

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Erythemato-Papulo-Squamous Diseases

Cited by 16 publications

References 303 publications

Papuloerythroderma of Ofuji: A Report of Two Cases

Papuloerythroderma of Ofuji: A Report of Two Cases

Palmoplantar Lichen Planus Presenting with Vesicle‐Like Papules

Exfoliative Erythroderma

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