Zobrazeno 1 - 10
of 28
pro vyhledávání: '"C I, Harrington"'
Publikováno v:
The British journal of dermatology. 141(3)
Paraffin-based emollients are widely used in dermatological practice and are not usually absorbed through the skin. We report a case where transcutaneous transfer did occur in the context of damaged skin in Netherton's syndrome, resulting in a revers
Publikováno v:
The British journal of dermatology. 138(4)
An 83-year-old woman presented with a vulval mass. Radical vulvectomy was performed and histology showed a unique mixed picture of spindle, pseudoglandular and classical squamous cell carcinoma arising in vulval lichen sclerosus.
Autor:
F M, Lewis, C I, Harrington
Publikováno v:
The Journal of reproductive medicine. 42(3)
Publikováno v:
The British journal of dermatology. 135(1)
The overall prevalence of vulval involvement in women with lichen planus is unknown. In a series of 37 women with lichen planus, we found vulval lesions in 19 (51%). Vulval lesions are often chronic and may undergo malignant change. All patients pres
Publikováno v:
Clinical and experimental dermatology. 21(2)
Pyoderma gangrenosum (PG) of the scrotum is extremely rare. We report a case of scrotal PG associated with dermatomyositis. Initial healing was slow despite the use of oral prednisolone and azathioprine. Healing was accelerated by the local use of a
Publikováno v:
BMJ. 305:955-955
Publikováno v:
BMJ. 303:925-925
Autor:
N W Read, C I Harrington
Publikováno v:
BMJ. 1:872-875
To clarify the controversy about the effectiveness of a gluten-free diet in dermatitis herpetiformis, 10 highly motivated patients were investigated. The indices used to assess improvement included deposition of sub-epidermal IgA in unaffected skin,
Autor:
C I Harrington
Publikováno v:
International Journal of Clinical Practice. 43:27-29
Publikováno v:
Acta dermato-venereologica. 66(2)
Most reports of skin malignancy associated with varicose ulceration have described carcinomatous change (1). The development of fibrosarcoma in varicose ulcers is considerably rare but has also been described (2). We report a case of angiosarcoma dev