Surgical management and oncological follow‐up of cutaneous squamous cell carcinomas arising in epidermolysis bullosa patients

A Paganelli, E Giordano, C Fiorentini… - International Journal …, 2022 - Wiley Online Library
Background Hereditary epidermolysis bullosa (EB) is a rare genodermatosis characterized
by skin fragility and blistering of the skin and mucous membranes in reaction to minimal …

LINC00641 Inhibits the Development of Cutaneous Squamous Cell Carcinoma By Downregulating miR-424 in A431 Cells

W Liu, X Liu - Cancer biotherapy & radiopharmaceuticals, 2021 - liebertpub.com
Background: Cutaneous squamous cell carcinoma (CSCC) is the most deadly disease
among nonmelanoma skin cancers. LINC00641 plays a role in various cancers, but its role …

Reconstruction with free jejunal flap in dystrophic epidermolysis bullosa complicated with hypopharyngeal cancer: A case report

D Matsumoto, N Otani, S Seike, T Kubo - Microsurgery, 2024 - Wiley Online Library
Epidermolysis bullosa (EB) encompasses a range of rare genetic dermatological conditions
characterized by mucocutaneous fragility and a predisposition to blister formation, often …

Épidermolyses bulleuses héréditaires: protocole national de diagnostic et de soins (PNDS)

C Chiaverini, E Bourrat, J Mazereeuw-Hautier… - … de Dermatologie et de …, 2017 - Elsevier
Résumé Les épidermolyses bulleuses héréditaires (EBH) sont un groupe hétérogène de
maladies génétiques rares caractérisées par une fragilité cutanée et/ou muqueuse …

[图书][B] Therapy development for epidermolysis bullosa

JP Hofbauer, V Wally, C Guttmann-Gruber, I Gratz… - 2021 - books.google.com
Although rare genodermatoses such as Epidermolysis bullosa have received more attention
over the last years, no approved treatment options targeting causal mutations are currently …

[PDF][PDF] Squamous Cell Carcinoma Arising in Chronic Inflammatory Dermatoses

D Kuraitis, A Murina - Cutis, 2024 - cdn.mdedge.com
30 I CUTIS® WWW. MDEDGE. COM/DERMATOLOGY how SCCs behave depending on
their location. Cohorts from China, 5 India, 6 and Japan7 have noted a higher rate of SCC …

Simple and affordable soft brace application in dystrophic epidermolysis bullosa patients

C Wu, XH Jiao - Frontiers in Surgery, 2024 - frontiersin.org
Background Dystrophic epidermolysis bullosa (DEB) is a hereditary disease characterized
by increased fragility of the epidermis and mucosa and is accompanied by blister formation …

Epidemiology and providing of healthcare for patients with inherited epidermolysis bullosa in the Russian Federation

AA Kubanov, AA Karamova… - Annals of the …, 2018 - vestnikramn.spr-journal.ru
Background: Inherited epidermolysis bullosa is a group of genetic skin disorders. In most
severe forms, such as junctional and dystrophic subtypes, quality of life and life expectancy …

Epidermolysis bullosa

C Has - Braun-Falco´ s Dermatology, 2022 - Springer
The term “hereditary epidermolysis bullosa”(EB) covers clinically and genetically
heterogeneous diseases associated with blisters of the skin and mucous membranes after …

Overview of complications associated with epidermolysis bullosa: A multicenter retrospective clinical analysis of 152 cases

E Raboei, A Alabdali, Y Owiwi, Y Yousef… - Journal of Pediatric …, 2021 - Elsevier
Abstract Background/Purpose Epidermolysis bullosa (EB) is a rare disease of skin and
mucosa which may causes surgical complications. We review these in a large patient cohort …