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先天性额骨缺损,头皮覆盖完整。

Congenital frontal bone defect with intact overlying scalp.

作者信息

Chakrabortty S, Oi S, Suzuki H, Izawa I, Yamaguchi M, Tamaki N, Matsumoto S

机构信息

Department of Neurosurgery, Kobe University School of Medicine, Japan.

出版信息

Childs Nerv Syst. 1993 Dec;9(8):485-7. doi: 10.1007/BF00393559.

DOI:10.1007/BF00393559
PMID:8124680
Abstract

An unusual case of a congenital frontal bone defect with intact overlying scalp and intact underlying dura mater is reported. Although spontaneous healing by the intact underlying dura mater by regeneration was expected, it did not occur. Cranioplasty was done for protective and cosmetic purposes. A review of the literature of congenital skull defects shows that spontaneous regeneration does not occur in this rare anomaly.

摘要

报道了一例先天性额骨缺损的罕见病例,其覆盖头皮完整,硬脑膜下层完整。尽管预期硬脑膜下层会通过再生实现自发愈合,但并未发生。为了保护和美观目的进行了颅骨成形术。对先天性颅骨缺损文献的回顾表明,这种罕见异常情况不会发生自发再生。

相似文献

1
Congenital frontal bone defect with intact overlying scalp.先天性额骨缺损,头皮覆盖完整。
Childs Nerv Syst. 1993 Dec;9(8):485-7. doi: 10.1007/BF00393559.
2
Long-term follow up of a growing skull fracture treated by dura and cranioplasty with artificial dura mater and methylmethacrylate.采用人工硬脑膜和甲基丙烯酸甲酯进行硬脑膜修补及颅骨成形术治疗儿童生长性颅骨骨折的长期随访
Childs Nerv Syst. 1997 Jun;13(6):349-51. doi: 10.1007/s003810050095.
3
Congenital frontal bone defect with intact overlying scalp.先天性额骨缺损,头皮覆盖完整。
Childs Nerv Syst. 1994 Jul;10(5):284. doi: 10.1007/BF00335164.
4
Acrylic frontal cranioplasty.
Head Neck Surg. 1986 Sep-Oct;9(1):32-41. doi: 10.1002/hed.2890090107.
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[Recurring intradiploic epidermoid cyst of the skull: a case report].[颅骨复发性板障内表皮样囊肿:一例报告]
No Shinkei Geka. 1998 Jul;26(7):633-7.
6
[Cranial bone prosthesis made of acrylic resins and prepared before surgical operation--description of the method].[手术前制备的丙烯酸树脂颅骨假体——方法描述]
Neurol Neurochir Pol. 1992;Suppl 1:310-5.
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The prognosis of cranioplasty following large craniectomy in children.儿童大骨瓣开颅术后颅骨修补的预后
Z Kinderchir. 1988 Dec;43(6):375-83. doi: 10.1055/s-2008-1043488.
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Hydroxylapatite cranioplasty directly over dura.硬脑膜上方直接进行羟基磷灰石颅骨成形术。
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The diagnosis of infections associated with acrylic cranioplasties.与丙烯酸颅骨修补术相关感染的诊断
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引用本文的文献

1
Aplasia cutis congenita of the scalp: is there a better treatment strategy?先天性头皮皮肤发育不全:是否存在更好的治疗策略?
Childs Nerv Syst. 2006 Sep;22(9):1072-9. doi: 10.1007/s00381-006-0074-y. Epub 2006 Apr 26.
2
Development in harmony.
Childs Nerv Syst. 2004 Oct;20(10):693-701. doi: 10.1007/s00381-004-1013-4. Epub 2004 Aug 24.
3
Congenital frontal bone defect with intact overlying scalp.先天性额骨缺损,头皮覆盖完整。
Childs Nerv Syst. 1994 Jul;10(5):284. doi: 10.1007/BF00335164.

本文引用的文献

1
Congenital perforations of the skull in relation to the parietal bone.与顶骨相关的先天性颅骨穿孔
J Neurosurg. 1962 Feb;19:153-8. doi: 10.3171/jns.1962.19.2.0153.
2
[APLASIA CUTIS CONGENITA. (DESCRIPTION OF A CASE IN THE PRODUCT OF INCEST)].[先天性皮肤发育不全。(乱伦产物中一例病例的描述)]
Folia Hered Pathol (Milano). 1964 Dec;14:35-48.
3
[Aseptic gangrene of the cranium as hereditary circumscribed aplasia of the newborn].[颅骨无菌性坏疽作为新生儿遗传性局限性发育不全]
Acta Genet Med Gemellol (Roma). 1963 Apr;12:117-33.
4
Congenital absence of the scalp and skull.先天性头皮和颅骨缺失。
Ann Surg. 1956 Dec;144(6):1035-44. doi: 10.1097/00000658-195612000-00014.
5
Conservative management of congenital defect of skull and scalp.先天性颅骨和头皮缺损的保守治疗
Surg Neurol. 1982 Feb;17(2):152-5. doi: 10.1016/s0090-3019(82)80046-3.
6
Nonsurgical approach to congenital scalp and skull defects.先天性头皮和颅骨缺损的非手术治疗方法。
J Neurosurg. 1982 May;56(5):711-5. doi: 10.3171/jns.1982.56.5.0711.
7
Congenital defect of scalp and skull in three generations of one family; case report.一个家族三代人的头皮和颅骨先天性缺陷;病例报告
Plast Reconstr Surg. 1970 Aug;46(2):194-6. doi: 10.1097/00006534-197008000-00029.
8
Evolution and significance of giant parietal foramina. Report of five cases in one family.巨大顶骨孔的演变及意义。一个家族中5例报告。
J Neurosurg. 1972 Oct;37(4):487-92. doi: 10.3171/jns.1972.37.4.0487.
9
Familial incidence of foramina parietalia permagna.顶骨大孔的家族发病率。
Neurochirurgia (Stuttg). 1987 Jan;30(1):25-7.
10
Congenital midline scalp and skull defect.先天性中线头皮和颅骨缺损。
Arch Dis Child. 1975 Dec;50(12):958-60. doi: 10.1136/adc.50.12.958.