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Final clinical diagnosis in cases of histopathologic psoriasiform dermatitis: retrospective cross-sectional analysis of a Southeastern United States population, 2004-2017.
Arch Dermatol Res
January 2025
Department of Dermatology, Duke University Medical Center, Durham, NC, USA.
Background: Psoriasiform dermatitis can be defined both clinically and histologically, but is not a traditionally recognized clinical or histologic diagnosis.
Objective: Analyze the final clinical diagnosis, demographics and clinical characteristics in patients with histologic psoriasiform dermatitis.
Methods: Retrospective cross-sectional analysis of patients with histologic psoriasiform dermatitis 2004-2017.
Pityriasis Lichenoides Chronica-Like Mycosis Fungoides: A Diagnostic Dilemma.
Skinmed
January 2025
Department of Skin & VD, Civil Hospital, BJ Medical College, Ahmedabad, Gujarat, India.
Mycosis fungoides (MF) is a neoplasm of the immune system. It is a cutaneous lymphoma originating in the peripheral epidermotropic T-cells, specifically the memory T-cells (CD45RO+). The etiology of MF is indefinite, but various factors, such as genetic and epigenetic abnormalities, environmental and occupational exposure to chemicals, infections, and cytokines (interleukin [IL]-2, IL-4, etc.
View Article and Find Full Text PDFParapsoriasis en plaque, deciphered at single-cell resolution.
J Allergy Clin Immunol
December 2024
Department of Dermatology, University of California, San Francisco, Calif. Electronic address:
Dermatological dichotomy: Atopic dermatitis or mycosis fungoides?
Asia Pac Allergy
December 2024
Allergy and Clinical Immunology Department, Coimbra University Hospital Centre, Coimbra, Portugal.
Article Synopsis
- Atopic dermatitis (AD) and mycosis fungoides (MF) can be difficult to distinguish because they exhibit similar symptoms like inflamed and itchy skin lesions.
- A case study of a 19-year-old male with a past AD history highlights the diagnostic confusion when he developed atypical eczema-like lesions that required advanced testing to confirm MF after initial misdiagnosis.
- The case underscores the importance of accurate and early diagnosis to differentiate between AD and MF, as MF requires specific treatments, and it encourages further research into shared mechanisms for improved patient care.
Introduction: Lymphocytic esophagitis (LyE) is a rare esophageal disorder of unknown etiology, characterized by dense peripapillary lymphocytes without neutrophils or eosinophils, and spongiosis. Patients typically present with symptoms such as dysphagia or chest pain. Here, we describe a notable case of lymphocytic esophagitis in a patient who presented with food impaction.
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