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家族性色素性荨麻疹

Familial urticaria pigmentosa.

作者信息

Fowler J F, Parsley W M, Cotter P G

出版信息

Arch Dermatol. 1986 Jan;122(1):80-1.

PMID:3455808
Abstract

Urticaria pigmentosa, characterized by cutaneous mast cell proliferation, usually occurs sporadically in childhood and resolves over a period. Rarely is the condition seen in two or more members of a family. We encountered a family in which urticaria pigmentosa occurred in four members of two generations. Skin findings were similar in all four. No systemic manifestations other than occasional flushing episodes were noted in any of the affected individuals. HLA typing was performed, but no significant correlation between affected and unaffected individuals was seen. In a review of a number of previously reported cases, we found a slight female preponderance.

摘要

色素性荨麻疹以皮肤肥大细胞增殖为特征,通常在儿童期散发出现,并在一段时间后消退。这种疾病很少在一个家族的两个或更多成员中出现。我们遇到了一个家族,其中两代四人都患有色素性荨麻疹。这四人的皮肤表现相似。在任何受影响的个体中,除了偶尔的潮红发作外,没有发现其他全身表现。进行了HLA分型,但未发现患病个体与未患病个体之间存在显著相关性。在回顾许多先前报道的病例时,我们发现女性略占多数。

相似文献

1
Familial urticaria pigmentosa.家族性色素性荨麻疹
Arch Dermatol. 1986 Jan;122(1):80-1.
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Familial urticaria pigmentosa.家族性色素性荨麻疹
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Familial urticaria pigmentosa: report of a family and review of the role of KIT mutations.家族性色素性荨麻疹:一家系报告及KIT突变作用的综述
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[HLA-DRW grouping in obstructive myocardiopathy].[阻塞性心肌病中的人类白细胞抗原-DRw分型]
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引用本文的文献

1
Diffuse Cutaneous Mastocytosis: A Current Understanding of a Rare Disease.弥漫性皮肤肥大细胞增生症:一种罕见疾病的当前认识。
Int J Mol Sci. 2024 Jan 23;25(3):1401. doi: 10.3390/ijms25031401.
2
Targeted Treatment Options in Mastocytosis.肥大细胞增多症的靶向治疗选择
Front Med (Lausanne). 2017 Jul 20;4:110. doi: 10.3389/fmed.2017.00110. eCollection 2017.
3
Urticaria pigmentosa in a child with Prader-Labhart-Willi syndrome.患有普拉德-威利综合征的儿童的色素性荨麻疹。
J Am Acad Dermatol. 1989 Jul;21(1):147-8. doi: 10.1016/s0190-9622(89)80361-5.