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巨大的后颅窝骨质侵蚀及其重建:“巨大枕大池”的一种特殊表现。

Massive posterior cranial vault erosion and its reconstruction: A peculiar presentation of "mega cisterna magna".

作者信息

Bansal Adity, Reddy Gosla Srinivas, Chug Ashi, Damaraju Sriram Chandra

机构信息

Department of Dentistry (Cranio-maxillofacial Surgery), AIIMS, Rishikesh, Uttarakhand, 249203, India.

GSR Institute of Craniofacial Surgery, Vinaynagar Colony, Saidabad, Hyderabad, Telangana, 500059, India.

出版信息

J Oral Biol Craniofac Res. 2021 Jan-Mar;11(1):13-16. doi: 10.1016/j.jobcr.2020.11.010. Epub 2020 Nov 12.

Abstract

Dandy-Walker (DW) complex is a rare central nervous system malformation, commonly associated with complex non-neurological conditions, defined by four variants with characteristic anatomic features, still inadequately known for its etiological aspects. "Mega Cisterna Magna" (MCM) is a type of DW complex which is represented by an enlarged posterior cranial fossa. Though reduction cranioplasty has been reported in enlarged posterior cranial fossa malformations, however we report a peculiar case of MCM with massive posterior cranial bone erosion, presenting completely asymptomatic at an age of 8 years, without any associated co-morbidities till date, nor with any evident occipital mass at birth. Survival of the child till this age is an exception in itself, but this can probably be explained by the presence of the giant defect of the posterior cranial bone, which must have acted like a vent and prevented the elevation of the ICP. Hence no symptoms were observed till date. Ventriculo-peritoneal (VP) shunting was done to drain the accumulated fluid, followed by massive cranioplasty, which was challenging and was performed with autologous cranial and fibular bone grafts, along with alloplastic titanium mesh, and thus achieving marked aesthetic improvement with satisfactory bone healing at a 3-year follow-up.

摘要

丹迪-沃克(DW)复合体是一种罕见的中枢神经系统畸形,通常与复杂的非神经系统疾病相关,由具有特征性解剖特征的四种变体定义,其病因方面仍知之甚少。“巨大枕大池”(MCM)是DW复合体的一种类型,表现为后颅窝扩大。虽然已有报道对后颅窝扩大畸形进行颅骨成形术,但我们报告了一例特殊的MCM病例,该病例后颅颅骨大量侵蚀,8岁时完全无症状,至今无任何相关合并症,出生时也无明显枕部肿块。该患儿存活至这个年龄本身就是一个例外,但这可能可以通过后颅骨巨大缺损的存在来解释,该缺损一定起到了通风口的作用,防止了颅内压升高。因此至今未观察到任何症状。进行了脑室-腹腔(VP)分流以引流积聚的液体,随后进行了大规模颅骨成形术,这具有挑战性,采用了自体颅骨和腓骨移植以及异体钛网进行手术,在3年随访时实现了显著的美学改善和令人满意的骨愈合。

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本文引用的文献

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