Areolar and periareolar pityriasis versicolor
Areolar and periareolar pityriasis versicolor
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乳晕和乳晕周围花斑癣
DOI:
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发表时间:
2004
影响因子:
9.2
通讯作者:
JM Weinberg
中科院分区:
文献类型:
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作者:
BL Smith;EK Koestenblatt;JM Weinberg
The present study included 23 consecutive patients with rosacea diagnosed between May 2000 and March 2002. Patients receiving oral and/or topical therapy for rosacea were excluded. A 4-mm lesional punch biopsy specimen was obtained from exposed facial skin of each patient. In addition, nonlesional, unexposed skin from the postauricular area was biopsied in nine patients. Immunohistochemical analysis was performed by the ethylenediaminetetraacetic acid (EDTA)-based antigen retrieval technique. The classical avidin–biotin–peroxidase method and diaminobervzidine (DAB) chromogen were applied for demonstration of androgen receptors (M3562 monoclonal; dilution 1 : 40; DAKO, Glostrup, Denmark). Androgen receptor status was assessed by counting the positively stained cells per 1000 cells. The patients with rosacea comprised two males and 21 females. The age range was 18–70 years (mean 45.2 years). The duration of the disease varied from 1 to 25 years (mean 4.7 years; median 3.00 years). Seven (30.4%) patients had erythematotelangiectatic, 15 (65.2%) had papulopustular and one (4.3%) had granulomatous rosacea. Immunohistochemical examination showed that 22 (95.6%) of the 23 lesional and eight of nine (88.8%) nonlesional biopsy specimens expressed androgen receptors. In both lesional and normal skin, strong androgen receptor immunoreactivity was found within the nuclei of cells in sebaceous glands, hair follicles and the basal layer of the epidermis (figs 1 and 2). The mean androgen receptor counts in lesional and normal skin were 293.7727 ± 205.6483 and 248.8889 ± 231.9183, respectively. The Mann– Whitney U -test did not reveal a significant difference between the two groups ( U = 88 000; Z = − 0479; P = 0.632). There is a plenty of clinical evidence suggesting that rosacea may be a hormonal disorder. The vasomotor instability during menopause provokes flushing, when rosacea is frequently triggered or exacerbated. 1,2,5,6 Endocrine disorders have been documented in women with rosacea 7 and the disease is associated with abnormalities of androgen excess, including menstrual abnormalities, acne vulgaris, polycystic ovary syndrome and hirsuitismus. 3,6 Moreover, antiandrogenic treatment modalities (oestrogens and cyproterone acetate) are reported to be effective in female patients with rosacea, providing a decrease in flushing and even complete recovery of papulopustular lesions. 6,8 Exogenous oestrogens are known to decrease excessive androgens and depress sebaceous gland secretion. 9 Their efficacy in rosacea suggests that higher local androgen concentrations may play a role at least in the development of follicular papulopustules of rosacea. Although serum oestrogen and androgen levels, sebum secretion and sebum lipid composition have been consistently normal in rosacea, 5 the role of local cutaneous endocrine milieu has not been clarified. The androgen action in most tissues is mediated through the androgen receptor. 10 We hypothesized that demonstration of an enhanced expression of androgen receptors within lesional skin (as compared with the normal skin) could provide supportive evidence for a role of androgens in the pathogenesis of rosacea. To the best of our knowledge, androgen receptor status in rosacea has been previously investigated only by Schmidt et al . 5
影响因子:
13.8
作者:
McPhaul,MJ;Young,M
通讯作者:
Young,M