Results 51 to 60 of about 2,887 (195)

Sclerosing diseases of the skin

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 10, Page 1282-1301, October 2025.
Summary Sclerosing skin diseases comprise a group of distinct dermatological conditions characterized by fibrotic changes that may severely impair patients’ quality of life. These conditions often present with cutaneous manifestations and, in some cases, may extend to extracutaneous tissues, potentially resulting in significant morbidity and mortality.
Yasamin Kalantari, Katharina Meier, Kamran Ghoreschi, Maria Kinberger, Farzan Solimani   +4 more
wiley   +1 more source

Acral papular mucinosis: a new case of this rare entity [PDF]

Anais Brasileiros de Dermatologia, 2016
Acral persistent papular mucinosis (APPM) is a rare subtype of localized lichen myxedematosus. It consists of small papules localized exclusively on the back of the hands, wrists and extensor aspects of distal forearms with no other clinical or ...
María Encarnación Gómez Sánchez, Fernando de Manueles Marcos, Maria Luisa Martínez Martínez, Roberto Vera Berón, Jose Manuel Azaña Défez   +4 more
doaj   +1 more source

Monoclonal Gammopathies of Clinical Significance—Scleromyxedema: A Case Report and Literature Review

Clinical Case Reports, Volume 13, Issue 8, August 2025.
ABSTRACT Scleromyxedema is an uncommon, chronic connective tissue disorder with an obscure etiology. It is distinguished by fibromyxoid skin lesions and elevated serum monoclonal immunoglobulin levels. The condition's rarity limits epidemiological data, making prevalence and incidence assessment difficult.
Shanshan Liang, Jingjing Zeng, Peiying Zhong, Chengyao Jia, Li Zhang   +4 more
wiley   +1 more source

Epidermal Nevi and Epidermal Naevus Syndromes

JEADV Clinical Practice, Volume 4, Issue 3, Page 669-680, August 2025.
ABSTRACT Epidermal nevi (EN) arise from postzygotic variants in ectoderm‐derived cell lines, such as keratinocytes and cells forming adnexa. EN may be present alone without any associated abnormality or be part of a syndrome. In this review, we will discuss about the clinical and genetics of the main types of EN and related syndromes.
Gianluca Tadini, Beatrice Carcano, Michela Brena   +2 more
wiley   +1 more source

SCLEROMYXEDEMA [PDF]

Acta Medica Iranica, 1996
Scleromyxedema is a rare, chronic, progressive, fibromucinous disorder of unknown etiology, characterized by lichenoid waxy papules and firm induration of skin of trunk, face, forearm and hands; fibroblast proliferation and mucin deposition in the upper ...
Z. Safaii Naraghi., P. Mansouri M.R. Mortazavi   +1 more
doaj   +2 more sources

Frictional alopecia of the distal legs: case series and review [PDF]

, 2016
BackgroundAcquired alopecia of the lower legs may occur secondary to friction due to socks, footwear, or both on the lower extremities. There is scant literature that reports on this phenomenon.Methods and MaterialsWe describe 5 patients who presented ...
Cohen, Philip R, Zhao, Johnny
core   +2 more sources

Reticular erythematous mucinosis: Relationship between its dermoscopic and histopathological findings

Clinical Case Reports, 2023
Key Clinical Message In reticular erythematous mucinosis, (1) the presence of dotted vessels and (2) uniform, structureless, yellowish‐white spots, and patches on dermoscopy correspond to histopathological findings of (1) vessels at the tips of the ...
Tomoaki Takada
doaj   +1 more source

گزارش يکصد مورد آميلوئيدوز ماکولر [PDF]

, 2002
آميلوئيدوز ماکولر از جمله بيماريهايی است که در آسيا، خاورميانه، چين، آمريکای مرکزی و جنوبی شيوع بيشتری نسبت به اروپا و آمريکای شمالی دارد. اين مطالعه به منظور مقايسه توزيع بيماری در دو جنس، سن درگيری، فراوانی بيماری در مراجعين به درمانگاه پوست، نيز ...
راثی, عباس
core  

The canine era : the rise of a biomedical model [PDF]

, 2016
Since the annotation of its genome a decade ago, the dog has proven to be an excellent model for the study of inherited diseases. A large variety of spontaneous simple and complex phenotypes occur in dogs, providing physiologically relevant models to ...
Abecasis, Agler, Ahonen, Ahram, Arendt, Awano, Axelsson, Bannasch, Baranowska Korberg, Boyko, Broeckx, Cadieu, Cerda-Gonzalez, Clark, Cooke, Daetwyler, de Sluis, Decker, Downs, Dreger, Drogemuller, Drogemuller, ENCODE Project Consortium, Everts, FANTOM Consortium, Forman, Forman, Freedman, French FMF Consortium, Genome of the Netherlands Consortium, Grall, Grundberg, Guo, Hayward, Hoeppner, Hytonen, Karlsson, Karlsson, Ke, Kim, Kirkness, Koskinen, Kyostila, Lavrijsen, Lavrijsen, Lee, Leegwater, Lequarre, Lin, Lindblad-Toh, Liu, Lohi, Massey, Merveille, Motohashi, Newton, Olsson, Ostrander, Packer, Pang, Parker, Parker, Pennisi, Rands, Roque, Roque, Salmon Hillbertz, Sargan, Savolainen, Schmutz, Schoenebeck, Seppala, Shannon, Skipper, Stamatoyannopoulos, Stritzel, Sudmant, Sutter, Sutter, Sutter, Tang, Tengvall, Thalmann, Tietz, Tonomura, Vaysse, vonHoldt, Voorbij, Wang, Wang, Wayne, Wilbe, Willet, Wolf, Yokoyama, Yoshida, Yuzbasiyan-Gurkan, Zanna   +97 more
core   +1 more source

Oral focal mucinosis in a dog with brachycephalic obstructive airway syndrome

Veterinary Record Case Reports, Volume 13, Issue 2, June 2025.
Abstract Oral focal mucinosis is an uncommon disorder primarily reported in people and characterised by excessive hyaluronic acid production in the mucosa. This report describes a novel occurrence of oral focal mucinosis in a 3‐year‐old French Mastiff with brachycephalic obstructive airway syndrome, presenting with severe respiratory distress and mucin
Daiana R. Cardoso, João Martins, Ana Resendes, Sónia Campos   +3 more
wiley   +1 more source