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色素失禁症:脑部改变的磁共振成像表现

Incontinentia pigmenti: MR demonstration of brain changes.

作者信息

Pascual-Castroviejo I, Roche M C, Martinez Fernández V, Perez-Romero M, Escudero R M, Garcia-Peñas J J, Sanchez M

机构信息

Service of Pediatric Neurology, Hospital Infantil "Las Paz," Madrid, Spain.

出版信息

AJNR Am J Neuroradiol. 1994 Sep;15(8):1521-7.

PMID:7985573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8334416/
Abstract

PURPOSE

To describe the MR findings in eight girls and women with incontinentia pigmenti, from two families. Four had skin lesions and neurologic disease, and four had only skin lesions.

METHODS

Eight patients had physical examination, family history, electroencephalogram and MR examination of the brain. MR was repeated in the two cases with more severe changes several years after the first study.

RESULTS

MR revealed brain changes only in the four patients who had neurologic disease associated with the cutaneous lesions of incontinentia pigmenti. Abnormalities were located in the cerebral hemisphere contralateral to the most affected side of the body. In two cases, the MR changes were subjacent to the scalp areas where the most severe cutaneous lesions were located in the neonatal period. Hypoplasia of the corpus callosum, probably secondary to atrophy of one or both cerebral hemispheres, and abnormal signal and atrophy of the lateral regions of one of the cerebellar hemispheres also were found in all four cases. Although the changes were seen in both the T1- and T2-weighted images, they were most evident in the latter. The four patients in the fourth stage who had only cutaneous lesions without neurologic problems did not reveal any MR abnormalities.

CONCLUSIONS

This study demonstrates MR signal changes and focal atrophy of the cerebrum, cerebellum, and corpus callosum in patients with incontinentia pigmenti and neurologic disorders. The MR images appear normal in patients with incontinentia pigmenti who have no neurologic abnormalities.

摘要

目的

描述来自两个家族的8名患有色素失禁症的女孩和女性的磁共振成像(MR)表现。其中4名有皮肤病变和神经系统疾病,4名仅有皮肤病变。

方法

8名患者接受了体格检查、家族史调查、脑电图检查以及脑部MR检查。对其中2例病变较严重的患者在首次检查几年后再次进行了MR检查。

结果

MR仅在4名患有与色素失禁症皮肤病变相关的神经系统疾病的患者中发现脑部改变。异常位于身体最受影响一侧对侧的大脑半球。在2例中,MR改变位于新生儿期皮肤病变最严重的头皮区域下方。在所有4例中还发现胼胝体发育不全,可能继发于一侧或双侧大脑半球萎缩,以及一侧小脑半球外侧区域的信号异常和萎缩。虽然在T1加权像和T2加权像上均可见这些改变,但在T2加权像上最为明显。处于第四阶段的4名仅有皮肤病变而无神经系统问题的患者未发现任何MR异常。

结论

本研究证明了患有色素失禁症和神经系统疾病的患者大脑、小脑和胼胝体的MR信号改变和局灶性萎缩。对于没有神经系统异常的色素失禁症患者,MR图像显示正常。

相似文献

1
Incontinentia pigmenti: MR demonstration of brain changes.色素失禁症:脑部改变的磁共振成像表现
AJNR Am J Neuroradiol. 1994 Sep;15(8):1521-7.
2
[Incontinentia pigmenti: clinical and neuroimaging findings in a series of 12 patients].色素失禁症:12例患者的临床及神经影像学表现
Neurologia. 2006 Jun;21(5):239-48.
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Central nervous system involvement in incontinentia pigmenti: cranial MRI of two siblings.
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Cerebral Arteriopathy in a Newborn With Incontinentia Pigmenti.患有色素失禁症的新生儿的脑动脉病
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Neurological findings in incontinentia pigmenti; a review.色素失禁症的神经学表现;综述
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Abnormal white matter in a neurologically intact child with incontinentia pigmenti.色素失禁症患儿神经系统正常但白质异常。
Pediatr Neurol. 2007 Mar;36(3):199-201. doi: 10.1016/j.pediatrneurol.2006.11.009.
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Incontinentia pigmenti: clinical and neuroradiologic features.
Brain Dev. 1993 Sep-Oct;15(5):362-6. doi: 10.1016/0387-7604(93)90122-o.
8
[Cerebral white matter lesions in a case of incontinentia pigmenti with infantile spasms, mental retardation and left hemiparesis].
No To Hattatsu. 1991 May;23(3):278-83.
9
Severe neuroimaging anomalies are usually associated with random X inactivation in leucocytes circulating DNA in X-linked dominant Incontinentia Pigmenti.严重的神经影像学异常通常与 X 连锁显性遗传性尿失禁型色素失禁症白细胞循环 DNA 中的随机 X 染色体失活有关。
Mol Genet Metab. 2017 Nov;122(3):140-144. doi: 10.1016/j.ymgme.2017.07.001. Epub 2017 Jul 10.
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Neonatal seizures in two sisters with incontinentia pigmenti.患有色素失禁症的两姐妹出现新生儿惊厥。
Neuropediatrics. 2004 Apr;35(2):139-42. doi: 10.1055/s-2004-815837.

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Hypomelanosis of Ito: a round on the frequency and type of epileptic complications.伊藤色素减退症:癫痫并发症的发生率及类型研究
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A Female Child with Skin Lesions and Seizures: Case report of Incontinentia Pigmenti.一名患有皮肤病变和癫痫发作的女童:色素失禁症病例报告
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Serial changes in white matter lesions in a neonate with incontinentia pigmenti.
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Therapy resistant neonatal seizures, linear vesicular rash, and unusually early neuroradiological changes: incontinentia pigmenti: a case report, literature review and insight into pathogenesis.耐药性新生儿惊厥、线状水疱性皮疹及异常早期的神经影像学改变:色素失禁症:一例报告、文献综述及发病机制探讨
Eur J Pediatr. 2008 Sep;167(9):979-83. doi: 10.1007/s00431-007-0618-5. Epub 2007 Oct 16.
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Diffuse cortical necrosis in a neonate with incontinentia pigmenti and an encephalitis-like presentation.患有色素失禁症且有脑炎样表现的新生儿出现弥漫性皮质坏死。
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