Results 51 to 60 of about 68,502 (175)

Granulomatous rosacea: Like leukemid in a patient with acute myeloid leukemia [PDF]

Vojnosanitetski Pregled, 2008
Introduction. Skin findings in leukemias may be divided into specific lesions (leukemia cutis) and non-specific lesions (leukemids) which may be found in up to 80% of all patients with leukemias.
Škiljević Dušan, Čolović Milica, Bogatić Dragana, Popadić Svetlana, Medenica Ljiljana   +4 more
doaj   +1 more source

A Case of Peripheral Odontogenic Myxofibroma Arising in the Palatal Gingiva of the Maxillary Second Premolar Region: A Case Report

Case Reports in Dentistry, Volume 2026, Issue 1, 2026.
Odontogenic myxofibroma (OMF) is a rare benign mesenchymal odontogenic tumor characterized by myxoid stroma with a prominent fibrous component. Although it usually arises intraosseously within the jaws, the peripheral variant, peripheral odontogenic myxofibroma (POMF), which occurs in extraosseous soft tissues, is uncommon and may be clinically ...
Masanori Masui, Hirokazu Yutori, Ai Fujimura, Soichiro Ibaragi, Hannah Wesley   +4 more
wiley   +1 more source

Topical Imiquimod in Mycosis Fungoides: A Systematic Review of Published Clinical Evidence

Dermatologic Therapy, Volume 2026, Issue 1, 2026.
Background Topical imiquimod has been used as a skin‐directed treatment in selected patients with mycosis fungoides, but the available evidence remains limited and scattered across case reports, case series, pilot studies, retrospective cohorts, and preliminary conference data.
Kerem Balan, Feyza Nur Akcin Balan, Suraiya Saleem   +2 more
wiley   +1 more source

A case of nodular cutaneous lupus mucinosis and literature review

Pifu-xingbing zhenliaoxue zazhi
Objective To report a case of nodular cutaneous lupus mucinosis and review relevant literature, in order to improve understanding of the disease. Methods We analyzed the clinical and histopathological features of a patient with nodular cutaneous lupus ...
Yuying YAO, Xiqing LI, Jianchi MA, Yijin LUO, Fengjie LIU   +4 more
doaj   +1 more source

Follicular mucinosis associated with mycosis fungoides.

, 1991
We report a patient who developed erythematous indurated plaques with alopecia on the face and multiple well-demarcated infiltrated scaling lesions on the trunk and extremities.
Rufli T, Büchner SA, Meier M
core   +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

55 | PAEDIATRIC FOLLICULAR MUCINOSIS WITHOUT PROGRESSION TO MYCOSIS FUNGOIDES: A LONG-TERM CLINICOPATHOLOGIC STUDY

Dermatology Reports
Background. Follicular mucinosis (FM), also known as alopecia mucinosa, is a rare clinicopathologic entity characterized by mucin deposition within the follicular epithelium, with or without sebaceous gland involvement [1,2].
Associazione Dermatologi-Venereologi Ospedalieri Italiani e della Sanità Pubblica
doaj   +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