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1
Hypomelanosis of Ito with gynaecomastia and dental anomaly.伊藤色素减退症伴男性乳房发育和牙齿异常。
BMJ Case Rep. 2018 Jul 6;2018:bcr-2018-225055. doi: 10.1136/bcr-2018-225055.
2
Hypomelanosis of Ito: streaks and whorls.伊藤色素减退症:条纹和涡状纹。
BMJ Case Rep. 2019 Apr 23;12(4):e227693. doi: 10.1136/bcr-2018-227693.
3
Palmoplantar depigmentation in Macaca fascicularis following Blaschko linear pattern.猕猴掌跖部色素脱失呈 Blaschko 线性分布模式。
J Med Primatol. 2020 Feb;49(1):52-55. doi: 10.1111/jmp.12445. Epub 2019 Oct 28.
4
Hypomelanosis of Ito with unusual associations.
Clin Exp Dermatol. 1997 Nov;22(6):295-6.
5
Coexistence of two neurocutaneous syndromes: tuberous sclerosis and hypomelanosis of Ito.两种神经皮肤综合征并存:结节性硬化症和伊藤色素减退症。
Indian J Dermatol Venereol Leprol. 2007 Jan-Feb;73(1):43-5. doi: 10.4103/0378-6323.30652.
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Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report.伴有2号染色体三体镶嵌现象的伊藤色素减退症:一例报告
J Med Case Rep. 2014 Oct 9;8:333. doi: 10.1186/1752-1947-8-333.
7
Hypomelanosis of Ito.伊藤色素减退症。
Indian J Pediatr. 2022 Nov;89(11):1117-1119. doi: 10.1007/s12098-022-04208-x. Epub 2022 Jun 22.
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Hypomelanosis of ito with trisomy 13 mosaicism [46, XY, der (13;13) (q10;q10), +13/46,xy].伴有13三体镶嵌现象的伊藤色素减退症[46,XY,der(13;13)(q10;q10),+13/46,xy]
Turk J Pediatr. 2002 Apr-Jun;44(2):152-5.
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[Hypomelanosis of Ito in a girl with Trisomy 13 mosaicism: a cytogenetic study].[一名患有13三体嵌合体的女孩的伊藤色素减退症:细胞遗传学研究]
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Hypomelanosis of Ito presenting with unilateral dilation of Virchow-Robin spaces: a case report.伊藤氏色素减退症表现为单侧脉络丛间隙扩张:一例报告。
Childs Nerv Syst. 2021 Sep;37(9):2931-2934. doi: 10.1007/s00381-021-05083-1. Epub 2021 Feb 13.

本文引用的文献

1
Psoriasis and Incontinentia Pigmenti Achromians.银屑病与色素失禁症性色素脱失症。
Indian J Dermatol Venereol Leprol. 1988 Mar-Apr;54(2):111-112.
2
The neurologic aspects of hypomelanosis of Ito: Case report and review of the literature.伊藤色素减退症的神经学表现:病例报告及文献综述
Sudan J Paediatr. 2014;14(2):61-70.
3
Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report.伴有2号染色体三体镶嵌现象的伊藤色素减退症:一例报告
J Med Case Rep. 2014 Oct 9;8:333. doi: 10.1186/1752-1947-8-333.
4
Hypomelanosis of Ito with an unusual pulmonary abnormality in an infant.一名患有异常肺部病变的婴儿的伊藤色素减退症。
Indian Dermatol Online J. 2014 Apr;5(2):196-7. doi: 10.4103/2229-5178.131109.
5
Cutaneous mosaicisms: concepts, patterns and classifications.皮肤镶嵌现象:概念、模式与分类
An Bras Dermatol. 2013 Jul-Aug;88(4):507-17. doi: 10.1590/abd1806-4841.20132015.
6
Hypomelanosis of ITO. A study of 76 infantile cases.伊藤色素减少症。76例婴儿病例的研究。
Brain Dev. 1998 Jan;20(1):36-43. doi: 10.1016/s0387-7604(97)00097-1.
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Hypomelanosis of Ito: diagnostic criteria and report of 41 cases.
Pediatr Dermatol. 1992 Mar;9(1):1-10. doi: 10.1111/j.1525-1470.1992.tb00317.x.

伊藤色素减退症伴男性乳房发育和牙齿异常。

Hypomelanosis of Ito with gynaecomastia and dental anomaly.

作者信息

Gupta Mudita, Gupta Pragya, Sharma Reena, Gupta Archit

机构信息

Department of Dermatology, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India.

Department of Surgery, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India.

出版信息

BMJ Case Rep. 2018 Jul 6;2018:bcr-2018-225055. doi: 10.1136/bcr-2018-225055.

DOI:10.1136/bcr-2018-225055
PMID:29982187
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6040523/
Abstract

Hypomelanosis of Ito is a rare neurocutaneous syndrome. Cutaneous involvement is characterised by streaks and swirls of hypopigmentation arranged in a Blaschkoid pattern. Neural involvement along with other systemic features are seen. We report a case of a 13-year-old boy who presented with the characteristic skin involvement of hypomelanosis of Ito, mental retardation, teeth abnormalities and gynaecomastia along with psoriasis.

摘要

伊藤色素减退症是一种罕见的神经皮肤综合征。皮肤受累的特征是色素减退的条纹和漩涡,呈布拉斯科线样分布。可见神经受累以及其他全身特征。我们报告一例13岁男孩,其表现为具有伊藤色素减退症特征性的皮肤受累、智力发育迟缓、牙齿异常、男性乳房发育以及银屑病。