Results 41 to 50 of about 1,099 (201)

A single plaque on the chin [PDF]

, 2021
Versión publicada - versión final del ...
Calderón Herschman, Perla Estrella, González Cuevas, Rubén Wladimir, Ortega Peña, Macarena, Peruilh Bagolini, Leonardo Andrés, Vargas Mora, Pablo Andrés   +4 more
core   +1 more source

Mucinose Folicular: revisão da literatura e relato de um caso Follicular mucinosis: literature review and case report

Anais Brasileiros de Dermatologia, 2002
A mucinose follicular (MuF), também chamada de alopecia mucinosa, é mucinose cutânea caracterizada pelo acúmulo de mucina no folículo pilossebáceo. As mucinoses têm duas formas de apresentação: uma idiopática ou primária, e outra sintomática ou associada
Antônio de Pádua Marques da Fonseca, Sebastião Honório Bona, Wanda Silveira M. da Fonseca, Francisco Soares Campelo, Prisco Medeiros de Melo Rego   +4 more
doaj   +1 more source

S3 guideline diagnostics and therapy of alopecia areata – Part 1: Diagnostics and epidemiology

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary In the project funded by the Innovation Committee at the G‐BA, the S3 guideline for the diagnosis and treatment of AA was developed between 2023 and 2025. The interdisciplinary expert panel consisted of representatives from the German Dermatological Society, in particular from the Pediatric Dermatology Working Group, the Professional ...
Ulrike Blume‐Peytavi, Andria Constantinou, Tsenka Tomova‐Simitchieva, Adrian Tanew, Michael Sticherling, Hermann Girschick, Annika Vogt, Uwe Schwichtenberg, Uwe Gieler, André Märtens, Kerstin Zienert, Claudia Stenders, Ricardo Niklas Werner, Doris Wilborn   +13 more
wiley   +1 more source

Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management

Dermatologic Therapy, Volume 2026, Issue 1, 2026.
Folliculotropic mycosis fungoides (FMF) is a rare subtype of MF, characterized by prominent folliculotropism in histopathology. Clinically, FMF exhibits polymorphic presentations, mainly including follicular papules, plaques, alopecia, and other nonspecific lesions, with a predilection for the head and neck region, leading to frequent misdiagnosis ...
Xingyu Li, Jie Liu, Nicola Pimpinelli
wiley   +1 more source

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

Skin‐Colored Papules on the Face and Chest of a Female Patient

Clinical Case Reports, Volume 13, Issue 9, September 2025.
ABSTRACT Scleromyxedema is an unpredictable but progressive disease and can be lethal due to systemic involvement if not diagnosed timely. Hence, we require a keen observational clinical eye to diagnose the condition from its differentials, along with further research into treatment modalities to treat this condition.
Mehdi Ghahartars, Seyyede Zeinab Azimi, Mojgan Akbarzadeh Jahromi, Mohammad Reza Namazi   +3 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

Paediatric cutaneous lymphomas including rare subtypes: A 40‐year experience at a tertiary referral centre

Journal of the European Academy of Dermatology and Venereology, Volume 39, Issue 1, Page 161-170, January 2025.
Abstract Background Primary cutaneous lymphomas are neoplasms of the immune system with a distinct tropism for the skin and an absence of extracutaneous manifestations at the time of diagnosis. Studies focusing on cutaneous lymphomas in children and adolescents remain scarce and often do not encompass the rare subtypes.
Silvia Alberti‐Violetti, Gianluca Avallone, Cristiana Colonna, Gianluca Tavoletti, Luigia Venegoni, Valentina Merlo, Stefano Cambiaghi, Angelo V. Marzano, Emilio Berti, Riccardo Cavalli   +9 more
wiley   +1 more source

Uncommon Presentation of Lepromatous Leprosy in a Nonendemic Setting: A Case Report

Case Reports in Medicine, Volume 2025, Issue 1, 2025.
Leprosy, caused by Mycobacterium leprae, remains a significant public health concern in certain endemic regions, but it is rarely encountered in nonendemic areas, posing diagnostic challenges. This case report discusses an unusual presentation of lepromatous leprosy in a patient residing in Saudi Arabia with no history of travel to endemic regions. The
Mhdia Elhadi Osman, Tareq Nafea Alharby, Yasser Alhabeeb, Ayman Elshenawy, Hala Ghazi Alreshidi, Saja Saleem Saja Saleem Alhayeti, Areej Alhumaidi Alshammari, Shamimul Hasan   +7 more
wiley   +1 more source

Successful Multimodal Therapeutic Approach for CD30‐positive Folliculotropic Mycosis Fungoides

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Chiara L. Blomen, Inga Hansen‐Abeck, Andrea Baehr, Stefan W. Schneider, Christoffer Gebhardt, Nina Booken   +5 more
wiley   +1 more source