Zobrazeno 1 - 10
of 15
pro vyhledávání: '"E. A. Fraser-Andrews"'
Autor:
Tracey J. Mitchell, Eduardo Calonje, Robin Russell-Jones, Sean Whittaker, Paul T. Seed, E. A. Fraser-Andrews, S Ferreira
Publikováno v:
British Journal of Dermatology. 155:756-762
Summary Background Histological evidence of lymph node involvement is associated with a poor prognosis in patients with cutaneous T-cell lymphoma (CTCL). Objectives To determine whether T-cell receptor (TCR) gene analysis is of prognostic relevance i
Autor:
Alun V. Evans, Robin Russell-Jones, E. A. Fraser-Andrews, Fiona Child, Alan Dean, Julia J. Scarisbrick, Sean Whittaker
Publikováno v:
Blood. 97:624-630
Erythrodermic cutaneous T-cell lymphoma (CTCL) includes patients with erythrodermic mycosis fungoides who may or may not exhibit blood involvement and Sézary syndrome and in whom hematological involvement is, by definition, present at diagnosis. Th
Autor:
A J Woolford, Guy Orchard, L.R. Whittam, Eduardo Calonje, E. A. Fraser-Andrews, Robin Russell-Jones
Publikováno v:
British Journal of Dermatology. 143:1199-1204
Background Childhood cases of cytotoxic T-cell lymphoma have not been well described. Objectives We have undertaken an immunohistochemical and genotypic analysis of patients presenting with juvenile onset mycosis fungoides (MF). Patients/methods Of 1
Publikováno v:
British Journal of Dermatology. 140:141-144
We report a 45-year-old man with mycosis fungoides (MF) who presented with multiple epidermoid cysts, comedones and alopecia and who responded to treatment with intravenous and oral cyclophosphamide. The pilotropic variant of MF, characterized histol
Publikováno v:
Clinical and Experimental Dermatology. 30:232-234
We report two patients in whom episodes of polymorphic light eruption were followed by recurrent erythema multiforme on exposed and nonexposed sites. Treating the polymorphic light eruption with prophylactic PUVA and/or oral prednisolone or cyclospor
Autor:
H. du P. Menagé, N. J. Manning, John A. McGrath, P. Eldridge, E. A. Fraser-Andrews, G. H. S. Ashton
Publikováno v:
Clinical and Experimental Dermatology. 28:203-205
We report a patient with the fish odour syndrome who has both primary and secondary trimethylaminuria. The diagnosis was made using biochemical and genetic analysis in the apparent absence of any characteristic smell. Differentiation of primary and s
Publikováno v:
Clinical and Experimental Dermatology. 26:683-685
We report a case of Sezary syndrome in a patient who was in the immediate vicinity of the Chernobyl nuclear reactor accident 18 months prior to presentation. A complex, frameshift p53 gene mutation was subsequently identified in tumour tissue, consis
Publikováno v:
Clinical and experimental dermatology. 28(2)
We report a patient with the fish odour syndrome who has both primary and secondary trimethylaminuria. The diagnosis was made using biochemical and genetic analysis in the apparent absence of any characteristic smell. Differentiation of primary and s
Autor:
E A, Fraser-Andrews, R, Russell-Jones, A J, Woolford, R A, Wolstencroft, A J, Dean, S J, Whittaker
Publikováno v:
Cancer. 92(7)
Sézary syndrome (SS) is characterized by erythroderma, peripheral lymphadenopathy, and circulating Sézary cells and is clinically heterogeneous.T-cell receptor (TCR) gene analysis was performed using DNA extracted from peripheral blood mononuclear
Publikováno v:
Clinical and experimental dermatology. 26(8)
We report a case of Sézary syndrome in a patient who was in the immediate vicinity of the Chernobyl nuclear reactor accident 18 months prior to presentation. A complex, frameshift p53 gene mutation was subsequently identified in tumour tissue, consi