Results 191 to 200 of about 19,701 (235)
Dermatological dichotomy: Atopic dermatitis or mycosis fungoides?
Pereira HP +4 more
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Retracted: Dermatological dichotomy: Atopic dermatitis or mycosis fungoides? [PDF]
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Critical Reviews in Oncology/Hematology, 2008
Mycosis fungoides (MF) constitutes the most frequent cutaneous T-cell lymphoma. Sezary syndrome is considered by some authors to be an erythrodermic leukemic variant of MF, but is classified separately in the new WHO-EORT classification of cutaneous lymphomas. MF usually occurs in old adults with a 2:1 male to female ratio.
ZINZANI, PIER LUIGI +2 more
openaire +8 more sources
Mycosis fungoides (MF) constitutes the most frequent cutaneous T-cell lymphoma. Sezary syndrome is considered by some authors to be an erythrodermic leukemic variant of MF, but is classified separately in the new WHO-EORT classification of cutaneous lymphomas. MF usually occurs in old adults with a 2:1 male to female ratio.
ZINZANI, PIER LUIGI +2 more
openaire +8 more sources
Surgical Pathology Clinics, 2014
This article is a comprehensive review of mycosis fungoides (MF), the most common type of cutaneous T-cell lymphoma. The first portion of the article introduces epidemiologic features of MF. Next, the clinical presentation is described, followed by the microscopic features.
openaire +2 more sources
This article is a comprehensive review of mycosis fungoides (MF), the most common type of cutaneous T-cell lymphoma. The first portion of the article introduces epidemiologic features of MF. Next, the clinical presentation is described, followed by the microscopic features.
openaire +2 more sources
Surgical Pathology Clinics, 2014
Mycosis fungoides (MF) is a cutaneous T-cell lymphoma that usually manifests as patches and plaques with a propensity for nonphotoexposed areas. MF is a common mimicker of inflammatory and infectious skin diseases, because it can be manifested with a wide variety of clinical and pathologic presentations.
M Estela, Martínez-Escala +2 more
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Mycosis fungoides (MF) is a cutaneous T-cell lymphoma that usually manifests as patches and plaques with a propensity for nonphotoexposed areas. MF is a common mimicker of inflammatory and infectious skin diseases, because it can be manifested with a wide variety of clinical and pathologic presentations.
M Estela, Martínez-Escala +2 more
openaire +2 more sources
Journal of Cutaneous Pathology, 2011
Mycosis fungoides (MF) represents the most common type of cutaneous T‐cell lymphoma (CTCL). CTCL often progresses through patch, plaque and tumor stages but can also manifest with varied clinical presentations. MF rarely presents in vesiculobullous fashion, in which vesicles or bullae develop in pre‐existing plaques or on the trunk or proximal ...
Joseph, Diehl +2 more
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Mycosis fungoides (MF) represents the most common type of cutaneous T‐cell lymphoma (CTCL). CTCL often progresses through patch, plaque and tumor stages but can also manifest with varied clinical presentations. MF rarely presents in vesiculobullous fashion, in which vesicles or bullae develop in pre‐existing plaques or on the trunk or proximal ...
Joseph, Diehl +2 more
openaire +2 more sources
New England Journal of Medicine, 2020
Advanced Mycosis Fungoides A 53-year-old man presented with rapidly progressing lesions on his face and body.
Hasina, Maredia, Sima, Rozati
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Advanced Mycosis Fungoides A 53-year-old man presented with rapidly progressing lesions on his face and body.
Hasina, Maredia, Sima, Rozati
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Follikulotrope Mycosis fungoides
Der Hautarzt, 2014Folliculotropic mycosis fungoides represents a rare variant of the CD4-positive cutaneous T-cell lymphoma mycosis fungoides. It is characterized by tropism of the lymphocytic infiltrate for hair follicle and other adnexal structures.Our patient presented with a 20-year history of pruritic skin lesions, which had been diagnosed as atopic dermatitis. The
J, Baratli, G, Balakirski, M, Megahed
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Extracutaneous mycosis fungoides
Cancer, 1987The clinical course of 40 patients with histologically documented extracutaneous mycosis fungoides (ECMF) was reviewed. Thirty one patients had documentation of nodal disease only (Stage IVA). Nine patients had histologic evidence of visceral involvement (Stage IVB).
C J, Merlo +3 more
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