Results 11 to 20 of about 368 (148)

Discrete papular lichen myxedematosus successfully treated with isotretinoin [PDF]

open access: yesJAAD Case Reports
Alexa Figueroa Baiges, BS   +2 more
doaj   +2 more sources

An unusual case of granulomatous scleromyxedema [PDF]

open access: yesJAAD Case Reports, 2022
Lauren Michelle, BA   +5 more
doaj   +2 more sources

Coexistence of mucinous nevus and multiple collagenoma with unilateral, dermatomal, and multi segmental distribution. [PDF]

open access: yesClin Case Rep, 2023
Deposition of amorphous materials in the high‐power field. Key Clinical Message Connective tissue nevus is a hamartoma composed of excess amounts of one or several components of the dermis, such as collagen, elastin, and proteoglycans. This report introduces a 14‐year‐old girl with grouped flesh color papules and skin color nodules distributed ...
Faghihi G   +4 more
europepmc   +2 more sources

Cutaneous Focal Mucinosis Successfully Treated With Superpulsed Carbon Dioxide Laser. [PDF]

open access: yesCase Rep Med
Cutaneous focal mucinosis (CFM) is a rare dermatological condition characterized by localized mucin deposition in the dermis, presenting as solitary or multiple asymptomatic papules or nodules. Treatment options are limited, with spontaneous resolution occurring in some cases, while others persist or require intervention.
Hekmat M   +3 more
europepmc   +2 more sources

Euthyroid Pretibial Mucinous Dermatoses: A Systematic Review of Current Evidence and the Controversy Surrounding Their Classification [PDF]

open access: yesActa Dermato-Venereologica
Ghassan Barnawi   +4 more
doaj   +2 more sources

A rare case of acral persistent papular mucinosis. [PDF]

open access: yesClin Case Rep, 2020
In patients with asymptomatic papules of hands and feet, a clinical differential of acral persistent papular mucinosis should be thought of. Abstract In patients with asymptomatic papules of hands and feet, a clinical differential of acral persistent papular mucinosis should be thought of.
Toh JJ, Goh NS, Wang DY.
europepmc   +2 more sources

Assessment of stigma related to visible skin diseases: a systematic review and evaluation of patient‐reported outcome measures

open access: yesJournal of the European Academy of Dermatology and Venereology, Volume 36, Issue 4, Page 499-525, April 2022., 2022
Abstract Misconceptions about visible skin diseases are widespread, and patients often face discrimination and stigmatization due to their condition. The associated negative health and psychosocial consequences of stigmatization in skin diseases have prompted an increase in research activity in recent times, resulting in a wide variety of assessment ...
C. Luck‐Sikorski   +5 more
wiley   +1 more source

Current development and future perspective of IDH1 inhibitors in cholangiocarcinoma

open access: yesLiver Cancer International, Volume 3, Issue 1, Page 17-31, February 2022., 2022
Abstract Background and Aims Biliary tract cancer (BTC) represents a major public health problem due to its increasing rates of incidence and mortality, especially the intrahepatic cholangiocarcinoma (IHCCA) subtype. First line palliative systemic treatment with cisplatin and gemcitabine has been the unique level IA evidence option until last few years
Jorge Adeva
wiley   +1 more source

Exome sequencing in patient‐parent trios suggests new candidate genes for early‐onset primary sclerosing cholangitis

open access: yesLiver International, Volume 41, Issue 5, Page 1044-1057, May 2021., 2021
Abstract BACKGROUND & AIMS Primary sclerosing cholangitis (PSC) is a rare bile duct disease strongly associated with inflammatory bowel disease (IBD). Whole‐exome sequencing (WES) has contributed to understanding the molecular basis of very early‐onset IBD, but rare protein‐altering genetic variants have not been identified for early‐onset PSC.
Sjoukje‐Marije Haisma   +19 more
wiley   +1 more source

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

open access: yesAnais 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   +4 more
doaj   +1 more source

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