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1
Becker's nevus syndrome with quadriparesis.伴有四肢瘫痪的贝克尔痣综合征
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Becker's nevus syndrome: case report.贝克尔痣综合征:病例报告。
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Becker's nevus syndrome: a case report.贝克氏痣综合征:病例报告。
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Bilaterally Asymmetrical Becker's Nevus.双侧不对称贝克痣。
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[Becker's nevus and hemimaxillary hypoplasia: coincidence or syndrome?].[贝克尔痣与半侧上颌骨发育不全:巧合还是综合征?]
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7
[The interesting case: unilateral hypoplasia of the breast in Becker nevus syndrome].[有趣的病例:贝克痣综合征中的单侧乳腺发育不全]
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Congenital Becker's nevus with a familial association.伴有家族关联的先天性贝克尔痣。
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Becker's nevus with ipsilateral breast hypoplasia: improvement with spironolactone.伴有同侧乳腺发育不全的贝克尔痣:螺内酯治疗有效
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本文引用的文献

1
Concurrent melanosis and hypertrichosis in distribution of nevus unius lateris.一侧痣分布区域并发黑变病和多毛症。
Arch Derm Syphilol. 1949 Aug;60(2):155-60. doi: 10.1001/archderm.1949.01530020023005.
2
Fractional resurfacing: a new therapeutic modality for Becker's nevus.分次嫩肤:治疗贝克尔痣的一种新疗法。
Arch Dermatol. 2007 Dec;143(12):1488-90. doi: 10.1001/archderm.143.12.1488.
3
Becker nevus syndrome.贝克尔痣综合征
Am J Med Genet. 1997 Jan 31;68(3):357-61.
4
Becker's nevus associated with limb asymmetry.贝克尔痣伴肢体不对称。
Arch Dermatol. 1981 Apr;117(4):243.
5
Becker's nevus: an androgen-mediated hyperplasia with increased androgen receptors.贝克尔痣:一种由雄激素介导的增生,伴有雄激素受体增加。
J Am Acad Dermatol. 1984 Feb;10(2 Pt 1):235-8. doi: 10.1016/s0190-9622(84)70029-6.
6
Becker's nevus and ipsilateral breast hypoplasia--androgen-receptor study in two patients.贝克尔痣与同侧乳腺发育不全——两名患者的雄激素受体研究
Arch Dermatol. 1992 Jul;128(7):992-3. doi: 10.1001/archderm.1992.01680170128025.

伴有四肢瘫痪的贝克尔痣综合征

Becker's nevus syndrome with quadriparesis.

作者信息

Fernandes Cecilia, Agrawal Ayushi, Shreshtha Binod Bade, Yogi Nikunj, Cherian Iype

机构信息

Department of Neurosurgery, Manipal College of Medical Sciences, Pokhara, Nepal.

出版信息

BMJ Case Rep. 2010 Dec 1;2010:bcr0620103117. doi: 10.1136/bcr.06.2010.3117.

DOI:10.1136/bcr.06.2010.3117
PMID:22798308
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3028056/
Abstract

A 12-year-old girl presented to Manipal Teaching Hospital with quadriparesis of 8 months' duration. Examination revealed a hyperpigmented patch over the chest wall with overlying hypertrichosis, musculoskeletal anomalies, upper limb asymmetry and ipsilateral breast hypoplasia. MRI scan revealed cranio-vertebral junction anomaly and spina bifida occulta at the cervical spine level. Histopathological examination of the skin revealed findings consistent with Becker's nevus. Based on the patient's clinical presentation and investigations, a diagnosis of Becker's nevus syndrome was made. However, she was managed conservatively as surgical intervention was not suitable in her case. The authors review Becker's nevus syndrome and its clinical manifestations below.

摘要

一名12岁女孩因持续8个月的四肢瘫痪入住马尼帕尔教学医院。检查发现胸壁有色素沉着过度斑块,其上有毛发过多、肌肉骨骼异常、上肢不对称和同侧乳房发育不全。MRI扫描显示颅颈交界区异常和颈椎水平隐性脊柱裂。皮肤组织病理学检查结果与贝克尔痣一致。根据患者的临床表现和检查,诊断为贝克尔痣综合征。然而,由于手术干预对她的情况不适用,她接受了保守治疗。作者在下文回顾了贝克尔痣综合征及其临床表现。