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伴有扁平皮肤病变的局限性背侧脊髓裂的手术组织病理学

Surgical histopathology of limited dorsal myeloschisis with flat skin lesion.

作者信息

Morioka Takato, Suzuki Satoshi O, Murakami Nobuya, Mukae Nobutaka, Shimogawa Takafumi, Haruyama Hironori, Kira Ryutaro, Iihara Koji

机构信息

Department of Neurosurgery, Fukuoka Children's Hospital, 5-1-1 Kashii-teriha, Higashi-ku, Fukuoka, 813-0017, Japan.

Department of Neuropathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

Childs Nerv Syst. 2019 Jan;35(1):119-128. doi: 10.1007/s00381-018-3870-2. Epub 2018 Jun 22.

Abstract

PURPOSE

Limited dorsal myeloschisis (LDM) is characterized by two invariable features: a focal closed neural tube defect and a fibroneural stalk linking the skin lesion to the underlying spinal cord. Although detailed histopathological findings of the LDM stalk were originally described by Pang et al., the precise relationship between the histopathological findings and clinical manifestations including intraoperative findings has not been fully determined.

METHODS

We retrospectively analyzed the histopathological findings of the almost entire stalk and their relevance to the clinical manifestations in six Japanese LDM patients with flat skin lesions.

RESULTS

Glial fibrillary acidic protein (GFAP)-immunopositive neuroglial tissues were observed in three of the six patients. Unlike neuroglial tissues, peripheral nerve fibers were observed in every stalk. In four patients, dermal melanocytosis, "Mongolian spot," was seen surrounding the cigarette-burn lesion. In three of these four patients, numerous melanocytes were distributed linearly along the long axis of the LDM stalk, which might represent migration of melanocytes from trunk neural crest cells during formation of the LDM stalk.

CONCLUSION

Immunopositivity for GFAP in the LDM stalk was observed in as few as 50% of our patients, despite the relatively extensive histopathological examination. We confirm that the clinical diagnosis of LDM should be made based on comprehensive histopathological examination as well as clinical manifestations. The profuse network of peripheral nerve fibers in every stalk and the high incidence of melanocyte accumulation associated with dermal melanocytosis might assist the histopathological diagnosis of LDM.

摘要

目的

局限性背侧脊髓纵裂(LDM)具有两个不变的特征:局灶性闭合性神经管缺陷以及连接皮肤病变与下方脊髓的纤维神经束。尽管Pang等人最初描述了LDM束的详细组织病理学发现,但组织病理学发现与包括术中发现在内的临床表现之间的确切关系尚未完全确定。

方法

我们回顾性分析了6例患有扁平皮肤病变的日本LDM患者几乎整个束的组织病理学发现及其与临床表现的相关性。

结果

在6例患者中的3例中观察到胶质纤维酸性蛋白(GFAP)免疫阳性的神经胶质组织。与神经胶质组织不同,在每个束中均观察到周围神经纤维。在4例患者中,在烟头状病变周围可见皮肤黑素细胞增多症,即“蒙古斑”。在这4例患者中的3例中,大量黑素细胞沿LDM束的长轴呈线性分布,这可能代表了LDM束形成过程中黑素细胞从躯干神经嵴细胞的迁移。

结论

尽管进行了相对广泛的组织病理学检查,但在我们的患者中,LDM束中GFAP免疫阳性的比例仅为50%。我们证实,LDM的临床诊断应基于全面的组织病理学检查以及临床表现。每个束中丰富的周围神经纤维网络以及与皮肤黑素细胞增多症相关的黑素细胞积聚的高发生率可能有助于LDM的组织病理学诊断。

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