Cas clinique : carcinome épidermoïde, lambeau antébrachial radial et syndrome d’Huriez. Mise au point sur une pathologie rare

Dumont, Léon; Gahagnon, T.; Martinot-Duquennoy, V.; Mortier, Laurent; Guerreschi, P.

doi:10.1016/j.anplas.2011.07.003

Cited by 2 publications

(1 citation statement)

References 16 publications

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“…[ 6 ] and Dumont et al . [ 7 ] also reported the association of SCC with Huriez syndrome in their patients along with surgical approach and possible ways of surgical management in such cases.…”

Section: Discussionmentioning

confidence: 99%

Huriez syndrome with superadded dermatophyte infection

Surana

Padhiar

Karia

et al. 2016

Indian Dermatol Online J

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Palmoplantarkeratodermas (PPKs) are a heterogeneous group of hereditary and acquired disorders with underlying gene defects, and characterized by hyperkeratosis of palms and soles with or without other ectodermal and systemic abnormalities. Huriez syndrome is a rare autosomal dominant transgradient type of PPK with high frequency of squamous cell carcinoma in the affected skin. We hereby describe a case of a very rare autosomal dominant PPK in a 40-year-old male patient presenting since birth with PPK extending onto the dorsal aspects of hands and feet with peeling of the skin. The complaints were associated with sclerodactyly, hyperhidrosis, and nail abnormalities. Also superadded dermatophyte infection was observed involving abdomen. No history of loss of any digit. No mucosal, dental, or any systemic involvement was present. No sign of malignancy was noted. Baseline investigations, including ultrasonography of abdomen were normal. Histological findings were nonspecific with only orthohyperkeratosis and acanthosis. Diagnosis was mainly done on clinical grounds. The patient is better with oral retinoids and topical emollients and keratolytics along with antifungal treatment for dermatophyte infection. He is under follow up.

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Section: Discussionmentioning

confidence: 99%

Huriez syndrome with superadded dermatophyte infection

Surana

Padhiar

Karia

et al. 2016

Indian Dermatol Online J

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Inherited Disorders of Cornification

Oji

Metze

Traupe

2016

Rook's Textbook of Dermatology, Ninth Edition

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The majority of keratinization disorders are referred to as Mendelian disorders of cornification. This is a very broad group, clinically characterized by hyperkeratosis or visible scaling or both. This chapter deals with the ichthyoses, palmoplantar keratodermas (PPKs) and miscellaneous cornification disorders such as porokeratoses. It is aimed primarily at dermatologists and physician scientists who have to make a clinical diagnosis and provide adequate management for their patients. Therefore a nosology and classification scheme has been chosen that is based on clinicogenetic and morphological features. Clinical diagnoses are then discussed with their molecular pathology. Part of the chapter addresses the management of congenital ichthyoses. Various tables provide an overview on clinical and/or pathophysiologically related groups of diseases. Finally, several cornification disorders are discussed that do not have a genetic basis, but are acquired or are of unknown aetiology (e.g. acquired ichthyoses/PPKs or perforating keratotic disorders).

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Cas clinique : carcinome épidermoïde, lambeau antébrachial radial et syndrome d’Huriez. Mise au point sur une pathologie rare

Cited by 2 publications

References 16 publications

Huriez syndrome with superadded dermatophyte infection

Huriez syndrome with superadded dermatophyte infection

Inherited Disorders of Cornification

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