Zobrazeno 1 - 10
of 3 915
pro vyhledávání: '"morphea"'
Autor:
Stephan R. Künzel, Erik Klapproth, Nick Zimmermann, Susanne Kämmerer, Mario Schubert, Karolina Künzel, Maximilian Hoffmann, Stephan Drukewitz, Anne Vehlow, Jiri Eitler, Marieke Arriens, Jessica Thiel, Romy Kronstein-Wiedemann, Maximiliane Tietze, Stefan Beissert, Bertold Renner, Ali El-Armouche, Claudia Günther
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-17 (2024)
Abstract Radiation-induced morphea (RIM) is a rare complication of radiotherapy presenting as inflammatory fibrosis, most commonly reported in breast cancer patients. As underlying disease mechanisms are not well understood, targeted therapies are la
Externí odkaz:
https://doaj.org/article/ca14d9c2e1744a85acf698b849bb68f5
Publikováno v:
Surgeries, Vol 5, Iss 3, Pp 758-763 (2024)
Radiation-induced morphea (RIM) is a progressive and irreversible scleroderma encountered after breast radiation therapy. This condition is often underdiagnosed, with confounding differentials including post-radiation fibrosis, infection, inflammator
Externí odkaz:
https://doaj.org/article/cfbf3eb056274870b63ab7e187bd9edb
Publikováno v:
JAAD Case Reports, Vol 49, Iss , Pp 135-139 (2024)
Externí odkaz:
https://doaj.org/article/b298abab78ec4c87afb5c2f0adf73560
Autor:
Maha Kazmi, BS, Katharina Shaw, MD, Winnie Fan, BS, Bianca Obiakor, BS, Ruth Ann Vleugels, MD, MPH, MBA, Anna Haemel, MD
Publikováno v:
JAAD International, Vol 18, Iss , Pp 27-29 (2025)
Externí odkaz:
https://doaj.org/article/94f862c4596042889d5a8a54b84a0e99
Autor:
Anzy N. Saleem, Ravi Kumar Krupanandan, Sudeep Kumar Kapalavai, Bala Ramachandran, Gopinathan Kathirvelu, Venkateswari Ramesh, Mahesh Janarthanan, Seyed Rabia, Ramkumar Ramamoorthy
Publikováno v:
Indian Pediatrics Case Reports, Vol 4, Iss 3, Pp 168-172 (2024)
Background: Linear scleroderma (LS) is a variant of localized scleroderma, which is termed as “en coup de sabre” (ECDS) when it involves the head and/or face. Although mainly a dermatological condition, extracutaneous manifestations have been inf
Externí odkaz:
https://doaj.org/article/39aa99d30b86409bb79cdf32c1badabb
Autor:
Alexy Hernandez, Leslie Zapata Leiva, Maria Mutka, Kathryn S. Torok, Leila Ledbetter, Christina K. Zigler
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-8 (2024)
Abstract Background Current treatment for localized scleroderma (LS) has been shown to halt disease activity, but little is still known about patient experiences with these treatments, nor is there consensus about optimal measurement strategies for f
Externí odkaz:
https://doaj.org/article/010b8909b664434498f715bd8f2b52c7
Publikováno v:
Clinical, Cosmetic and Investigational Dermatology, Vol Volume 17, Pp 1633-1636 (2024)
Khalid M Al-Husain,1 Abdulaziz Madani,2 Ahmed Alhumidi,3 Turky Alsehli,2 Khalid Nabil Nagshabandi2 1Department of Dermatology, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia; 2Department of Dermatology, College of M
Externí odkaz:
https://doaj.org/article/4424e032d76e420888e82bfe44989bb6
Autor:
Raza Khan, Amor Khachemoune
Publikováno v:
Indian Dermatology Online Journal, Vol 15, Iss 4, Pp 584-592 (2024)
Introduction: Morphea, an autoimmune progressive disorder, can significantly impact patient well-being, yet therapeutic options, though expanding, exhibit limited efficacy. A persistent challenge in disease management revolves around monitoring disea
Externí odkaz:
https://doaj.org/article/0001c3be9b9b43bc9b6e5d1aa8f8a0be
Publikováno v:
Hematology Reports, Vol 16, Iss 2, Pp 354-366 (2024)
Hypopigmentation disorders pose significant diagnostic challenges in dermatology, sometimes reflecting underlying hematological conditions. This review explores the clinical presentations related to hypopigmentation in hematological disorders, focusi
Externí odkaz:
https://doaj.org/article/baec80f76ace496684aee2db8c2df39d
Autor:
Selena Osman, MSc, Danya Traboulsi, MD
Publikováno v:
JAAD Case Reports, Vol 48, Iss , Pp 14-17 (2024)
Externí odkaz:
https://doaj.org/article/6635e8e3323141c3bbc8ed2c87c5fb0a