Results 41 to 50 of about 761 (169)

Follicular mucinosis: a clinicopathologic, histochemical, immunohistochemical and molecular study comparing the primary benign form and the mycosis fungoides-associated follicular mucinosis

, 2010
Objectives: To determine (i) whether primary (idiopathic) follicular mucinosis (PFM) and lymphoma-associated follicular mucinosis (LAFM) are distinct or related entities and whether there are reliable criteria that allow the two forms to be distinguished,
De Lucchi S, Meyes D, Rebora A, Zupo S, Patterson JW, Mora M, Cerruti G, Rongioletti F   +7 more
core   +2 more sources

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

Follicular lymphomatoid papulosis revisited: a study of 11 cases, with new histopathological findings [PDF]

, 2013
BACKGROUND: Follicular lymphomatoid papulosis (LyP) describes a variant of LyP with perifollicular infiltrates and some degree of folliculotropism of CD30(+) atypical lymphocytes. So far, only a few cases of follicular LyP have been described. OBJECTIVE:
Kempf, Werner, Baumgartner, Hans-Peter, Kutzner, Heinz, Heinz Kutzner, Dmitry V. Kazakov, Hans-Peter Baumgartner, Kazakov, Dmitry V, Werner Kempf   +7 more
core   +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

Syringolymphoid hyperplasia and follicular mucinosis in a patient with cutaneous T-cell lymphoma

, 1999
Syringolymphoid hyperplasia with alopecia is an uncommon chronic dermatosis of which 9 cases have been reported, with or without follicular mucinosis or cutaneous T-cell lymphoma.
Tannous, Zeina, Kvedar, Joseph, Duncan, Lyn M., Tannous, Z, Kvedar, J, Baldassano, M F, Baldassano, Marisa F., Duncan, L M, Li, Vincent W., Li, V W   +9 more
core   +1 more source

Cutaneous mucinosis in a strain of brown-egg laying chickens

, 2014
Cutaneous mucinosis is a cutaneous disorder described in humans, dogs, and rarely cats but never reported in birds. Twenty-six brown egg–laying chickens between ages 43 and 46 weeks had a history of feather loss, scaly, dry skin, weight loss, and ...
Anthenill, L., Palmieri, C., Shivaprasad, H. L.   +2 more
core   +2 more sources

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