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火棉胶婴儿与板层状鱼鳞病。

Collodion baby and lamellar ichthyosis.

作者信息

Sandler B, Hashimoto K

机构信息

Department of Dermatology & Syphilology, Wayne State University School of Medicine, Detroit, Michigan, USA.

出版信息

J Cutan Pathol. 1998 Feb;25(2):116-21. doi: 10.1111/j.1600-0560.1998.tb01699.x.

DOI:10.1111/j.1600-0560.1998.tb01699.x
PMID:9521501
Abstract

It is important to differentiate the collodion baby from harlequin ichthyosis as the latter rarely survives past the first few days of life. Occasionally, babies share features of both disorders and defy a clinical diagnosis. We recently encountered such a baby who initially presented with harlequin-like features, but evolved into lamellar ichthyosis once the keratin cast was shed. Since the routine histology of all these ichthyoses is similar, we used electron microscopy to study serial biopsy specimens from the affected infant on days 7, 14, and 150, and compared them to our own other cases of harlequin ichthyosis and lamellar ichthyosis. Electron microscopic studies of our case revealed that the marginal band of cornified cells of the stratum corneum was absent when the baby exhibited collodion/harlequin ichthyosis features. Another biopsy taken when the clinical picture evolved into lamellar-like ichthyosis, showed a well-formed marginal band in the cornified cells. In harlequin ichthyosis, the marginal band is present at birth. It is suggested that electron microscopy can differentiate severe collodion baby from harlequin ichthyosis at birth using the absence of the marginal band. Previously reported features of harlequin ichthyosis, such as the presence of giant mitochondria and an abnormal formation of the marginal band in luminal villi of acrosyringeal eccrine duct, were absent in our case.

摘要

将火棉胶婴儿与丑角样鱼鳞病区分开来很重要,因为后者很少能活过出生后的头几天。偶尔,婴儿会同时具有这两种疾病的特征,难以进行临床诊断。我们最近遇到了这样一个婴儿,其最初表现出丑角样特征,但一旦角质层外壳脱落,就演变成了板层状鱼鳞病。由于所有这些鱼鳞病的常规组织学表现相似,我们使用电子显微镜研究了该患病婴儿在第7天、14天和150天时的系列活检标本,并将其与我们自己的其他丑角样鱼鳞病和板层状鱼鳞病病例进行了比较。对我们这个病例的电子显微镜研究显示,当婴儿表现出火棉胶/丑角样鱼鳞病特征时,角质层的角化细胞边缘带缺失。当临床表现演变成板层样鱼鳞病时所取的另一次活检显示,角化细胞中有形成良好的边缘带。在丑角样鱼鳞病中,边缘带在出生时就存在。有人提出,电子显微镜可以通过边缘带的缺失在出生时将重症火棉胶婴儿与丑角样鱼鳞病区分开来。在我们的病例中,未出现先前报道的丑角样鱼鳞病特征,如巨大线粒体的存在以及顶泌汗腺导管腔绒毛中边缘带的异常形成。

相似文献

1
Collodion baby and lamellar ichthyosis.火棉胶婴儿与板层状鱼鳞病。
J Cutan Pathol. 1998 Feb;25(2):116-21. doi: 10.1111/j.1600-0560.1998.tb01699.x.
2
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引用本文的文献

1
Lamellar Icthyosis - A case Report.板层状鱼鳞病——病例报告
J Clin Diagn Res. 2014 Nov;8(11):ZD01-2. doi: 10.7860/JCDR/2014/9201.5108. Epub 2014 Nov 20.
2
Harlequin ichthyosis: a case report of prolonged survival.丑角样鱼鳞病:长期存活病例报告
BMJ Case Rep. 2014 Mar 7;2014:bcr2013200884. doi: 10.1136/bcr-2013-200884.
3
Expedient treatment of a collodion baby.火棉胶婴儿的快速治疗。
Case Rep Dermatol Med. 2011;2011:803782. doi: 10.1155/2011/803782. Epub 2011 Oct 15.
4
Identification, by homozygosity mapping, of a novel locus for autosomal recessive congenital ichthyosis on chromosome 17p, and evidence for further genetic heterogeneity.通过纯合性定位在17号染色体短臂上鉴定出常染色体隐性先天性鱼鳞病的一个新位点,并发现了进一步的遗传异质性证据。
Am J Hum Genet. 2001 Jul;69(1):216-22. doi: 10.1086/321284. Epub 2001 Jun 7.