Results 81 to 90 of about 4,210 (234)

Systematized epidermolytic epidermal nevus (ichthyosis hystrix) [PDF]

, 2015
Ichthyosis hystrix is a term used to describe an autosomal dominant rare form of an ichthyosiform dermatosis which is characterized by hyperkeratotic spiny scales. We present a healthy 22-year-old man with lesions which clinically and histopathologically
Guleva, Dimitrina, Kazandjieva, Jana, Márina, Sonya, Semkova, Kristina   +3 more
core   +2 more sources

Heterozygous DSP in‐frame deletion in a poodle with syndromic ichthyosis involving additional hair and tooth abnormalities

Animal Genetics, Volume 55, Issue 5, Page 725-732, October 2024.
Abstract Ichthyoses comprise a large heterogeneous group of skin disorders, characterized by generalized scaly and hyperkeratotic skin. We investigated a miniature poodle with early onset generalized scaling, dry and irregularly thickened skin, paw pad hyperkeratosis and abnormalities in hair and teeth.
Sarah Kiener, Georg Lehner, Vidhya Jagannathan, Monika Welle, Tosso Leeb   +4 more
wiley   +1 more source

Epidermal reaction patterns

Indian Journal of Dermatopathology and Diagnostic Dermatology, 2015
Changes in the epidermis serve as important histopathological clues to the diagnosis of skin disorders. These peculiar changes are referred to as epidermal reaction patterns.
Aanchal Panth, M Ramam
doaj   +1 more source

S3 guideline: Diagnosis and treatment of epidermal necrolysis (Stevens‐Johnson syndrome and toxic epidermal necrolysis) – Part 1: Diagnosis, initial management, and immunomodulating systemic therapy

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 10, Page 1448-1466, October 2024.
Summary Stevens‐Johnson syndrome and toxic epidermal necrolysis (SJS/TEN) are rare, predominantly drug‐induced, acute, life‐threatening diseases of skin and mucosae. SJS and TEN are nowadays considered variants of one disease entity with varying degrees of severity called epidermal necrolysis (EN). EN is associated with high morbidity and mortality and
Ruben Heuer, Maren Paulmann, Thorsten Annecke, Björn Behr, Katharina Boch, Anja M. Boos, Knut Brockow, Lars E. French, Jochen Gille, Verena Gundlach, Bernd Hartmann, Peter Höger, Silke C. Hofmann, Tobias Klein, Marcus Lehnhardt, Yvonne Liß, Philip Maier, Philipp Mandel, Nicos Marathovouniotis, Finnja Marlok, Hans Mittelviefhaus, Uwe Pleyer, Marie Pradeau, Katharina Rall, Siegbert Rieg, Heike Rittner, Frank Sander, Stefan Schnitzler, Christina Schut, Annette Stolle, Artem Vorobyev, Bettina Wedi, Johannes Weiss, Maximilian Zepp, Mirjana Ziemer, Maja Mockenhaupt, Alexander Nast   +36 more
wiley   +1 more source

Bullous Congenitalichthyosiform Erythroderma - PS 1 Type

Indian Journal of Dermatology, 2003
We describe a case of bullous congenital ichthyosiform erythroderma (epidermolytic hyperkeratosis) with severe transgradient type of palmoplantar keratoderma. It occurred in a thirty year old man, who was born out of first degree consanguineous marriage.
Dave Shriya, Rakhesh S. V, Thappa Devinder Mohan   +2 more
doaj  

Current surgical treatment options for ocular complications of Stevens-Johnson and Lyell's syndromes [PDF]

РМЖ "Клиническая офтальмология", 2023
V.F. Chernysh, N.N. Haritonova, A.N. Kulikov, P.A. Kacherovich, A.A. Kol'bin S.M. Kirov Military Medical Academy, St. Petersburg, Russian Federation Epidermolytic drug reactions (EDR) are severe acute drug-induced allergic disorders ...
V.F. Chernysh, N.N. Haritonova, A.N. Kulikov, P.A. Kacherovich, A.A. Kol'bin   +4 more
doaj  

Single dominant lesion in capillary malformation‐arteriovenous malformation (CM‐AVM) RASA1 syndrome

Pediatric Dermatology, Volume 41, Issue 5, Page 861-865, September/October 2024.
Abstract We report two cases with localized vascular malformations clinically resembling the “dominant lesion” seen in capillary malformation‐arteriovenous malformation (CM‐AVM) syndrome, however, lacking germline RASA1 variants but presenting double somatic RASA1 variants in affected tissue.
Luis Fernando Sánchez‐Espino, Marta Ivars, Carolina Prat Torres, Cinzia E. Lavarino, Nagore Gené Olaciregui, Carlota Rovira Zurriaga, Verónica P. Celis Passini, Miguel Bejarano Serrano, Eulàlia Baselga   +8 more
wiley   +1 more source

Keratin 9 L164P mutation in a Chinese pedigree with epidermolytic palmoplantar keratoderma, cytokeratin analysis, and literature review

Molecular Genetics & Genomic Medicine, 2019
Background Epidermolytic palmoplantar keratoderma (EPPK) is characterized by hyperkeratotic lesions on palms and soles. The disorder is caused by mutations of keratin 9 (KRT9) or KRT1 gene.
Xiaoliang Liu, Chuang Qiu, Rong He, Yuanyuan Zhang, Yanyan Zhao   +4 more
doaj   +1 more source

Ichthyosis associated with rickets in two Indian children

Indian Journal of Dermatology, 2013
We wish to report two cases of rickets due to vitamin D deficiency secondary to underlying ichthyotic skin disorder. The first case is of an 8-year-old male with history of multiple fluid-filled lesions over the body that would rupture to heal with ...
Dimple Kothari, Bhavana Doshi, Gaurav Garg, Uday S Khopkar   +3 more
doaj   +1 more source

Epidermal nevi and epidermolytic hyperkeratosis: A review of cases, highlighting indications for biopsy and genetics referral

Pediatric Dermatology, Volume 41, Issue 5, Page 780-785, September/October 2024.
Abstract Epidermal nevi are common benign cutaneous hamartomas that may rarely demonstrate histopathologic evidence of epidermolytic hyperkeratosis (EHK), representing cutaneous mosaicism for pathogenic keratin variants. Rarely, individuals with linear epidermal nevi transmit to their children the inherited form of EHK, also known as epidermolytic ...
Jessie M. Nelson, Jacqueline M. Isaac, Julie E. Mervak, Jennifer B. Mancuso, May P. Chan, Amanda Arreola, Kelly B. Cha   +6 more
wiley   +1 more source