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朗格汉斯细胞组织细胞增生症1例 被引量:1

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摘要 1病历摘要 患儿男,7个月。因全身丘疹、水疱、结痂5个月.于2009年4月7日来我院就诊。患儿5个月前无明显诱因头面部起黄豆大水疱,散在分布,逐渐累及躯干、四肢,皮损干涸、结痂后自行脱落,后皮损反复加重。患儿自发病以来,无发热、呕吐、腹泻。家族中无类似疾病史。
出处 《临床皮肤科杂志》 CAS CSCD 北大核心 2011年第10期638-639,共2页 Journal of Clinical Dermatology
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参考文献6

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二级参考文献23

  • 1高举,袁粒星.郎格汉斯细胞组织细胞增生症的诊断和治疗[J].实用儿科临床杂志,2006,21(15):1037-1040. 被引量:22
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共引文献26

同被引文献7

  • 1Satter EK, High WA. Langerhans cell histiocytosis: a review ofthe current recommendations of the Histiocyte Society[J]. PediatrDermatol, 2008, 25(3): 291-295.
  • 2Fernandes LB, Guerra JG, Costa MB, et al. Langerhans cellshistiocytosis with vulvar involvement and responding to ihalido-mide therapy--case report [J]. An Bras Dermatol, 2011, 86(4Suppl 1): S78-S81.
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  • 5Chang JC, Blake DG, I^ung BV, et al. Langerhans cell histiocyto-sis associated with lichen sclerosus of the vulva: case report andreview of the literature[J]. J Cutan Pathol, 2013, 40(2): 279-283.
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  • 7Foley S, Panting K, Bell H, et al. Rapid resolution of primaryvulval adult Langerhans cell histiocytosis with very potent topi-cal corticosteroids[J]. Australas J Dermatol, 2011, 52(1): e8-e!4.

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