Syringotropic and folliculotropic mycosis fungoides with mycosis fungoides–associated vasculopathic ulcers
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چکیده
منابع مشابه
Folliculotropic Mycosis Fungoides Associated with Autoimmune Hepatitis.
Dear Editor, the association between lymphomas and autoimmune manifestations, as well as the prevalence of the cases of coexistent lymphomas and autoimmune conditions, has not been completely established (1-3). Since cutaneous T-cell lymphoma (CTCL) cases are rare, any hypothesis can only be based on case reports or small case series. We present the case of a male patient with folliculotropic m...
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Folliculotropic mycosis fungoides is a variant of mycosis fungoides characterized by the presence of folliculotropic infiltrates, often with sparing of the epidermis, and preferential involvement of the head and neck. We report our experience with four cases of folliculotropic mycosis fungoides followed in our department in the last years. There are four patients (three men and one woman) aged ...
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Reports on clinical and histologic follicular alterations in patients previously diagnosed with mycosis fungoides (MF) or at the time of MF diagnosis are rare. The clinical and histologic criteria to distinguish MF associated with follicular mucinosis from follicular MF are a matter of debate. A patient is described with advanced clinical and histologic alterations predominated by follicular le...
متن کاملExceptional Association of Syringotropic Mycosis Fungoides with Chronic Lymphocytic Leukaemia.
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folliculotropic mycosis fungoides with comedonal-like appearances
conclusions fmf should be considered in patients who present with alopecia, acne like lesions, cysts and comedones in older ages with a spectrum of histologic changes. we emphasize for any time it should be under-recognized. introduction folliculotropic mycosis fungoides (fmf) is a variant of mycosis fungoides characterized by the presence of folliculotropic atypical tcells infiltrates, often w...
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ژورنال
عنوان ژورنال: JAAD Case Reports
سال: 2019
ISSN: 2352-5126
DOI: 10.1016/j.jdcr.2019.01.020