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Arteriovenous Malformations of the Temporalis Muscle: A Comprehensive Review.
Oper Neurosurg (Hagerstown)
April 2018
Maxillofacial Surgery Department, Hospital Clínico Universitario Virgen de la Arrixaca, El Palmar, Murcia, Spain.
Article Synopsis
- Arteriovenous malformations of the temporalis muscle (TM-AVMs) are rare lesions, distinct from scalp AVMs, featuring as large soft tissue masses in the temporal area, typically diagnosed in young patients.
- The study analyzed seven cases (5 from literature, 2 from the authors' database) to emphasize their unique characteristics, showing a mean diameter of 6 cm and slow evolution of up to 5 years before diagnosis.
- Surgical intervention was successful in all cases with complete removal and no recurrence, differentiating TM-AVMs from scalp AVMs, which usually present as high-flow lesions without the same tumor mass appearance.
Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening.
Br J Dermatol
May 2017
Department of Dermatology, University Hospital Crosshouse, Kilmarnock, U.K.
The inherited palmoplantar keratodermas (PPKs) are a heterogeneous group of genodermatoses, characterized by thickening of the epidermis of the palms and soles. No classification system satisfactorily unites clinical presentation, pathology and molecular pathogenesis. There are four patterns of hyperkeratosis - striate, focal, diffuse and punctate.
View Article and Find Full Text PDFEpidermal nevus.
Dermatol Online J
November 2010
Department of Dermatology, New York University, New York, NY, USA.
A healthy 25-year-old man presented with a widespread, non-organoid, non-epidermolytic epidermal nevus. In addition to extensive hyperpigented patches and thin plaques following Blaschko lines, there were superimposed psoriasiform plaques on the elbows and warty plaques on the upper trunk. Striate palmar keraoderma also was evident.
View Article and Find Full Text PDFNew syndrome of hypotrichosis, striate palmoplantar keratoderma, acro-osteolysis and periodontitis not due to mutations in cathepsin C.
Br J Dermatol
September 2002
Department of Dermatology, University Medical Centre St Radboud Nijmegen, PO Box 9101, 6500 HB Nijmegen, The Netherlands.
We report a mother and daughter with a syndrome of hypotrichosis, striate palmoplantar keratoderma, onychogryphosis, periodontitis, acro-osteolysis and psoriasis-like skin lesions. The syndrome resembles Papillon-Lefèvre syndrome (PLS), characterized by palmoplantar keratoderma, periodontitis and psoriasis-like skin lesions, and particularly Haim-Munk syndrome, an allelic variant of PLS with acro-osteolysis. Both are caused by mutations in the cathepsin C gene (CTSC).
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