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Alopecia areata
被引:470
|作者:
Pratt, C. Herbert
[2
]
King, Lloyd E., Jr.
[3
]
Messenger, Andrew G.
[4
]
Christiano, Angela M.
[5
,6
]
Sundberg, John P.
[1
,3
]
机构:
[1] Jackson Lab, Dept Res & Dev, 600 Main St, Bar Harbor, ME 04609 USA
[2] Jackson Lab, Dept Genet Resource Sci, 600 Main St, Bar Harbor, ME 04609 USA
[3] Vanderbilt Univ, Med Ctr, Dept Dermatol, Nashville, TN USA
[4] Royal Hallamshire Hosp, Dept Dermatol, Sheffield, S Yorkshire, England
[5] Columbia Univ, Dept Dermatol, New York, NY 10027 USA
[6] Columbia Univ, Dept Genet & Dev, New York, NY USA
来源:
NATURE REVIEWS DISEASE PRIMERS
|
2017年
/
3卷
关键词:
QUALITY-OF-LIFE;
CLOBETASOL PROPIONATE 0.05-PERCENT;
FOLLICLE IMMUNE PRIVILEGE;
GENOME-WIDE ASSOCIATION;
C3H/HEJ MOUSE;
AUTOIMMUNE-DISEASE;
PUVA TREATMENT;
FOLLOW-UP;
HAIR LOSS;
DEBR RAT;
D O I:
10.1038/nrdp.2017.11
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Alopecia areata is an autoimmune disorder characterized by transient, non-scarring hair loss and preservation of the hair follicle. Hair loss can take many forms ranging from loss in well-defined patches to diffuse or total hair loss, which can affect all hair-bearing sites. Patchy alopecia areata affecting the scalp is the most common type. Alopecia areata affects nearly 2% of the general population at some point during their lifetime. Skin biopsies of affected skin show a lymphocytic infiltrate in and around the bulb or the lower part of the hair follicle in the anagen (hair growth) phase. A breakdown of immune privilege of the hair follicle is thought to be an important driver of alopecia areata. Genetic studies in patients and mouse models have shown that alopecia areata is a complex, polygenic disease. Several genetic susceptibility loci were identified to be associated with signalling pathways that are important to hair follicle cycling and development. Alopecia areata is usually diagnosed based on clinical manifestations, but dermoscopy and histopathology can be helpful. Alopecia areata is difficult to manage medically, but recent advances in understanding the molecular mechanisms have revealed new treatments and the possibility of remission in the near future.
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