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Case of melorheostosis associated with ipsilateral verrucous epidermal nevus, linear connective tissue nevus, diffuse hyperpigmentation and hypertrichosis: A fortuitous coincidence?

作者信息

Di Altobrando Ambra, Neri Iria, Gurioli Carlotta, Misciali Cosimo, Baraldi Carlotta, Pedrini Elena, Gnoli Maria, Tremosini Morena, Sangiorgi Luca, Patrizi Annalisa

机构信息

Department of Experimental, Diagnostic and Specialty Medicine - Division of Dermatology, University of Bologna, Bologna, Italy.

Department of Medical Genetics and Rare Orthopedic Diseases, IRCCS Rizzoli Orthopedic Institute, Bologna, Italy.

出版信息

J Dermatol. 2020 Sep;47(9):1063-1066. doi: 10.1111/1346-8138.15460. Epub 2020 Jul 12.

Abstract

Melorheostosis (MEL) is a rare benign bone disorder that can be associated with several anomalies, including vascular abnormalities, nevus sebaceus, unilateral nevoid telangiectasia, linear scleroderma and hypertrichosis. We report the case of a 6-year-old patient who showed an unusual co-occurrence of bone hyperostosis and different skin lesions affecting the same side of the body: MEL, verrucous epidermal nevus, connective tissue nevus, linear scleroderma-like disorder, hyperpigmentation and hypertrichosis. The spatial co-occurrence of these conditions made us speculate as to whether they originated from a common genetic mechanism or if their co-occurrence was completely accidental.

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