Zobrazeno 1 - 10
of 19
pro vyhledávání: '"E Mary Wain"'
Publikováno v:
The American Journal of Dermatopathology. 43:e204-e212
Primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder and primary cutaneous marginal zone B-cell lymphoma are 2 distinct entities with several overlapping features which can result in diagnostic uncertainty. Clinically, they both fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83a11d2339387a644868bf19440d011f
https://doi.org/10.1097/dad.0000000000002003
https://doi.org/10.1097/dad.0000000000002003
Autor:
Alistair Robson, R.J. Barlow, Mina Ally, Werner Kempf, Ellie Rashidghamat, Zena N Willsmore, Ben Esdaile, Farrah Bakr, Danielle Greenblatt, Fiona Child, E. Mary Wain
Publikováno v:
The American Journal of dermatopathology. 43(12)
Introduction Primary cutaneous marginal zone B-cell lymphoma (MZL) follows an indolent clinical course. Histopathologically, there is a polymorphous infiltrate that includes small lymphocyte-like and centrocyte-like B cells and plasma cells usually w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::565546505fdbf9db8cd460c675dcfd09
https://pubmed.ncbi.nlm.nih.gov/34231493
https://pubmed.ncbi.nlm.nih.gov/34231493
Publikováno v:
British Journal of Hospital Medicine. 80:331-336
Recent improvements in post-transplant care have led to an increased life expectancy for recipients of organ transplants. These patients require lifelong immunosuppression, which is associated with an increased incidence of malignant disease. Skin ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4006111f26493846777f1e94ad67f0f5
https://doi.org/10.12968/hmed.2019.80.6.331
https://doi.org/10.12968/hmed.2019.80.6.331
Publikováno v:
The American Journal of dermatopathology. 43(12)
Primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder (PCSM-LPD), recently downgraded from a T-cell lymphoma, is a poorly characterized histopathological entity. Presenting as a solitary lesion that often grows rapidly, it may raise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c0873739f462deb769e57836edee5d1
https://pubmed.ncbi.nlm.nih.gov/33989212
https://pubmed.ncbi.nlm.nih.gov/33989212
Publikováno v:
Clinical Medicine. 12:160-164
Key Points Cutaneous T-cell lymphoma (CTCL) is an uncommon cutaneous malignancy that usually presents with patches and/or plaques, less commonly with tumours and/or haematological involvement Mycosis fungoides is usually an indolent condition that ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b26845664fa9109fb7e23af09bb9741e
https://doi.org/10.7861/clinmedicine.12-2-160
https://doi.org/10.7861/clinmedicine.12-2-160
Publikováno v:
Journal of the American Academy of Dermatology. 63:653-660
Background In frontal fibrosing alopecia (FFA), scalp alopecia dominates the clinical picture. However, eyebrow loss and hair loss in other body sites may also occur; this has been documented clinically, but rarely histopathologically. We describe th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6314da6c0227eb4b16b21d02e5dff3ae
https://doi.org/10.1016/j.jaad.2009.09.020
https://doi.org/10.1016/j.jaad.2009.09.020
Autor:
Rosalind Foster, Christine L. Jones, Chung-Ching Chu, Isabella Tosi, Sean Whittaker, Robert C.T. McKenzie, E. Mary Wain, Tracey J. Mitchell
Publikováno v:
Journal of Investigative Dermatology. 130(4):1116-1125
Sezary Syndrome (SS) is an aggressive leukemic variant of primary cutaneous T-cell lymphoma characterized by the presence of tumor or Sezary cells that generally display a mature memory T-cell immunophenotype. Sezary cells proliferate poorly and ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6431a51815e4b1b64b28a4046d6c4947
Publikováno v:
Journal of Cutaneous Pathology. 35:770-773
Genital herpes simplex virus (HSV) infection is usually a straightforward clinical diagnosis, rarely requiring histological confirmation. We report two cases of immunosuppressed patients in which the clinical and pathological features were initially
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c38fc93b41422b3e55e411d9f928b4c
https://doi.org/10.1111/j.1600-0560.2007.00899.x
https://doi.org/10.1111/j.1600-0560.2007.00899.x
Autor:
Susan Mayou, Klaus J. Misch, David J. Atherton, E. Mary Wain, Robin Russell-Jones, Guy Orchard
Publikováno v:
Journal of the American Academy of Dermatology. 53:158-163
We report 3 cases of mycosis fungoides (MF) with a CD56+ cytotoxic immunophenotype. Each patient presented with a different clinical phenotype: one exhibited limited poikilodermatous patches (skin stage T1); one, widespread hypopigmented lesions (ski
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e8a56394c07c84b7de566c18cb9d3eb
https://doi.org/10.1016/j.jaad.2005.01.133
https://doi.org/10.1016/j.jaad.2005.01.133
Publikováno v:
Cancer. 98:2282-2290
BACKGROUND Mycosis fungoides (MF) is predominantly a disease of older patients, but occasionally occurs in children. The aims of the current study were to describe the clinical presentation, pathologic features, and disease progression (DP) in patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a7b6786f52de4d31432fe84fefd89f4
https://doi.org/10.1002/cncr.11780
https://doi.org/10.1002/cncr.11780