Results 61 to 70 of about 2,893 (176)

Studies on Biological Factors in Acantholysis*

Journal of Investigative Dermatology, 1964
Recent interest in the biochemical mechanism of acantholysis has been spurred by Lever's (1) monograph in which he reported acantholysis to be diagnostic of pemphigus vulgaris. Acantholysis can be experimentally induced in human skin in a variety of ways.
openaire   +2 more sources

Cystic acantholytic dyskeratosis of the vulva: An unusual presentation of a follicular adnexal neoplasm

Indian Dermatology Online Journal, 2016
Acantholytic dyskeratosis (AD) is a histologic pattern seen in Darier's disease or dyskeratosis follicularis, warty dyskeratoma, and transient AD. This pattern is characterized by suprabasilar clefting, acantholysis, and formation of corps ronds and ...
Kara Melissa Tiangco Torres, Jacqueline M Junkins-Hopkins   +1 more
doaj   +1 more source

Warty (follicular) dyskeratoma on the mons pubis

International Journal of Women's Dermatology, 2017
Warty (follicular) dyskeratoma (WD) is a discrete nodular lesion that demonstrates the characteristic histopathologic findings of acantholysis and dyskeratosis. WDs most commonly occur on the head and neck of adults. We present a case of WD that occurred
P.E. Kerr, M.J. Murphy
doaj   +1 more source

Pemphigus foliaceus unveiled: a case report

MGM Journal of Medical Sciences
Pemphigus foliaceus is a rare, life-threatening autoimmune skin disorder characterized by acantholysis (loss of keratinocyte-to-keratinocyte adhesion), which causes blistering and erosion of the skin. P.
Sudhanshu Shukla, Tejashree Sridhar, Pratiksha Bhandare, Sanatkumar Bharamu Nyamagoud, Jayasheela S. Hiremath, A. H. M. Vishwanatha Swamy   +5 more
doaj   +1 more source

Experimental Human Cell and Tissue Models of Pemphigus

Dermatology Research and Practice, 2010
Pemphigus is a chronic mucocutaneous autoimmune bullous disease that is characterized by loss of cell-cell contact in skin and/or mucous membranes. Past research has successfully identified desmosomes as immunological targets and has demonstrated that ...
Gerda van der Wier, Hendri H. Pas, Marcel F. Jonkman   +2 more
doaj   +1 more source

Hailey-Hailey disease: clinical, diagnostic and therapeutic update [PDF]

Anais Brasileiros de Dermatologia
Hailey-Hailey disease is a rare genodermatosis described in 1939, with an autosomal dominant inheritance pattern, characterized by compromised adhesion between epidermal keratinocytes.
Adriana Maria Porro, Camila Arai Seque, Denise Miyamoto, Diego Vanderlei Medeiros da Nóbrega, Milvia Maria Simões e Silva Enokihara, Claudia Giuli Santi   +5 more
doaj   +1 more source

Rapid and long‐lasting remission of refractory Hailey‐Hailey disease by IL‐13 inhibition with tralokinumab

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 6, Page 818-820, June 2026.
Oliver Brandt, Stephanie M. Huber, Simon M. Mueller   +2 more
wiley   +1 more source

Subcorneal Pustular Dermatosis in Childhood: A Case Report and Review of the Literature

Case Reports in Dermatological Medicine, 2013
Subcorneal pustular dermatosis (SCPD, also known as Sneddon-Wilkinson disease) is a rare, benign, chronic, sterile pustular eruption which usually develops in middle-age or elderly women; it is rarely seen in childhood and adolescence.
Massimiliano Scalvenzi, Franco Palmisano, Maria Carmela Annunziata, Ernesto Mezza, Immacolata Cozzolino, Claudia Costa   +5 more
doaj   +1 more source

Galli–Galli Disease: A Comprehensive Literature Review

Dermatopathology
Galli–Galli disease (GGD) is a rare genodermatosis that exhibits autosomal dominant inheritance with variable penetrance. GGD typically manifests with erythematous macules, papules, and reticulate hyperpigmentation in flexural areas.
Andrea Michelerio, Antonio Greco, Dario Tomasini, Carlo Tomasini   +3 more
doaj   +1 more source

Grover disease associated with docetaxel chemotherapy

JAAD Case Reports, 2022
Shawn Afvari, BS, Melvin W. Chiu, MD, MPH   +1 more
doaj   +1 more source