Results 51 to 60 of about 3,765 (219)

Primary Cutaneous Gamma-Delta T-Cell Lymphoma With Long-Term Indolent Clinical Course Initially Mimicking Lupus Erythematosus Profundus

open access: yesFrontiers in Oncology, 2020
Primary Cutaneous Gamma-Delta (γδ) T-Cell Lymphoma (PCGDTCL) is a rare primary cutaneous lymphoma of aggressive nature. Only a few cases with an initially indolent course over years have been published.
Laura von Dücker   +7 more
doaj   +1 more source

Unusual Presentation of Subcutaneous Panniculitis‐Like T‐Cell Lymphoma

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Subcutaneous panniculitis‐like T‐cell lymphoma (SPTCL) is a rare variant of primary cutaneous T‐cell lymphoma primarily affecting subcutaneous adipose tissue and mimicking lobular panniculitis. It often presents with erythematous subcutaneous nodules or plaques, and diagnosis can be challenging due to its diverse clinical manifestations.
Mona Alkallabi   +6 more
wiley   +1 more source

World Association for Veterinary Dermatology Consensus Statement for Diagnosis, and Evidence‐Based Clinical Practice Guidelines for Treatment and Prevention of Canine Leishmaniosis

open access: yesVeterinary Dermatology, Volume 36, Issue 6, Page 723-787, December 2025.
Hyperkeratosis of (a) the footpads and (b) the nasal planum. ABSTRACT Background Canine leishmaniosis (CanL) due to Leishmania infantum remains common, and veterinarians do not always follow scientifically sound approaches for diagnosis, treatment and prevention. Objectives To provide consensus guidelines for diagnosis and evidence‐based guidelines for
Manolis N. Saridomichelakis   +9 more
wiley   +1 more source

Poststeroid Panniculitis in An Adult

open access: yesSiriraj Medical Journal, 2020
Poststeroid panniculitis is a rare complication of corticosteroid therapy. All reported cases have occurred in children. In this communication, we describe a 41-year-old woman who presented to us with multiple subcutaneous nodules which appeared after ...
Niyom Tantikun, Apichati Sivayathorn
doaj  

Type I Interferonopathies in Children: An Overview

open access: yesFrontiers in Pediatrics, 2021
Notable advances in gene sequencing methods in recent years have permitted enormous progress in the phenotypic and genotypic characterization of autoinflammatory syndromes.
Debora M. d'Angelo   +4 more
doaj   +1 more source

Lupus erythematosus profundus (lupus panniculitis) induced by interferon-beta in a multiple sclerosis patient [PDF]

open access: yes, 2007
ArticleJOURNAL OF CLINICAL NEUROSCIENCE.
Gono, T   +5 more
core   +1 more source

Atypical Manifestations of Old World Cutaneous Leishmaniasis: A Systematic Review and Clinical Atlas of Unusual Clinical and Specific Anatomical Presentations

open access: yesHealth Science Reports, Volume 8, Issue 9, September 2025.
ABSTRACT Background and Aims Cutaneous leishmaniasis (CL) represents the most common form of leishmaniasis. It imposes a significant medical burden due to long‐lasting ulcers and disfiguring scars, underscoring the need for comprehensive CL control strategies, particularly in endemic regions.
Bahareh Abtahi‐Naeini   +5 more
wiley   +1 more source

Cancer risk factors in systemic lupus erythematosus: multivariate regression analysis in 16,409 patients [PDF]

open access: yes, 2014
Peer ...
Anca Askanase   +41 more
core   +1 more source

The Role of Cutaneous B‐Cells in Hidradenitis Suppurativa: From Preclinical Evidence to Novel Targeted Therapies

open access: yesExperimental Dermatology, Volume 34, Issue 9, September 2025.
ABSTRACT Hidradenitis Suppurativa (HS) is a chronic autoinflammatory skin disease of the terminal hair follicle, whose pathogenesis is complex and multifactorial. Alongside a predisposing genetic background, environmental/epigenetic factors, alterations in the skin microbiome, and dysregulation of both innate and adaptive immune responses contribute to
Maurizio Romagnuolo   +6 more
wiley   +1 more source

Weber-Christian disease: ultrasound can see it [PDF]

open access: yes, 2014
Weber-Christian disease, also known as idiopathic relapsing febrile nodular non-suppurative panniculitis, is a rare inflammatory disorder of the subcutaneous tissue characterized by recurrent nodules often associated with constitutional symptoms, in ...
Cathryn Anne Scott, Paolo Agostinis
core   +2 more sources

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