Mycosis fungoides masquerading as cutaneous lupus erythematosus and associated with antiphospholipid syndrome
Identifieur interne : 001981 ( Main/Exploration ); précédent : 001980; suivant : 001982Mycosis fungoides masquerading as cutaneous lupus erythematosus and associated with antiphospholipid syndrome
Auteurs : E. C. Veysey [Royaume-Uni] ; J. D. Wilkinson [Royaume-Uni]Source :
- Clinical and Experimental Dermatology [ 0307-6938 ] ; 2008-01.
English descriptors
- Teeft :
- Actinic reticuloid, Amersham, Amersham hospital, Anticoagulant, Antiphospholipid, Antiphospholipid antibodies, Antiphospholipid antibody syndrome, Antiphospholipid syndrome, Atrophic epidermis, Basal liquefaction, Biopsy, Blackwell publishing, Cutaneous, Cutaneous lupus, Cutaneous lupus erythematosus, Cutaneous necrosis, Dense perifollicular, Dermatol, Dermatology, Erythematous, Experimental dermatology, Extensive involvement, Follicular, Follicular epithelium, Fungoides, Journal compilation, Lesion, Lupus, Lupus anticoagulant, Monoclonal population, Mycosis, Mycosis fungoides, Oral steroids, Photosensitive, Rash, Syndrome, Tumorous, Tumorous lesion, Upper dermis, Veysey, Wilkinson.
Abstract
We report a case of a 69‐year‐old woman with mycosis fungoides (MF), who presented with clinical and histological features of cutaneous lupus, and for 6 years was treated for this, until repeated biopsies and gene‐rearrangement studies confirmed a diagnosis of MF. In addition, she developed thromboemboli and was found to have lupus anticoagulant antibodies. The possible biological relationship between antiphospholipid antibody syndrome and MF is considered. To our knowledge, this is the first reported case of MF masquerading as cutaneous lupus.
Url:
DOI: 10.1111/j.1365-2230.2007.02546.x
Affiliations:
Links toward previous steps (curation, corpus...)
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- to stream Main, to step Curation: 001981
Le document en format XML
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<front><div type="abstract" xml:lang="en">We report a case of a 69‐year‐old woman with mycosis fungoides (MF), who presented with clinical and histological features of cutaneous lupus, and for 6 years was treated for this, until repeated biopsies and gene‐rearrangement studies confirmed a diagnosis of MF. In addition, she developed thromboemboli and was found to have lupus anticoagulant antibodies. The possible biological relationship between antiphospholipid antibody syndrome and MF is considered. To our knowledge, this is the first reported case of MF masquerading as cutaneous lupus.</div>
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