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钉突状血管瘤重新分类为浅表淋巴管畸形:52 例研究。

Hobnail hemangioma reclassified as superficial lymphatic malformation: a study of 52 cases.

机构信息

Department of Dermatology, Hospital de Cascais Dr José de Almeida, Lisbon, Portugal.

出版信息

J Am Acad Dermatol. 2012 Jan;66(1):112-5. doi: 10.1016/j.jaad.2011.05.019. Epub 2011 Aug 6.

Abstract

BACKGROUND

Hobnail hemangioma (HH) is currently classified as a benign vascular tumor, although it is not well understood whether this lesion differentiates toward blood or lymphatic endothelial cells. Immunostaining with the endothelial marker Wilms tumor 1 (WT1) helps distinguish between vascular neoplasms and malformations, being positive in the former and negative in the latter.

OBJECTIVE

We sought to investigate WT1, human herpesvirus 8 latent nuclear antigen, D2-40, and Ki-67 immunoprofile in HH, to gain further insight into its histogenesis.

METHODS

We evaluated 52 HHs collected in Dermatohistopathologische Gemeinschaftslabor, Friedrichshafen, Germany. Immunohistochemical expression of WT1 was performed in all cases. Ten of 52 lesions were also studied for D2-40 and Ki-67 staining and 12 lesions were stained for human herpesvirus 8 latent nuclear antigen.

RESULTS

All 52 HHs were completely negative for WT1 immunostaining. Immunohistochemistry performed in 10 HHs showed diffuse and strong positive staining for D2-40 in 8 lesions and focal positivity in two. All cases tested showed negative staining for Ki-67 and human herpesvirus 8 latent nuclear antigen.

LIMITATIONS

There are no limitations.

CONCLUSIONS

Although the exact histogenesis of HH is unknown, most of the performed immunohistochemical studies support a lymphatic line of differentiation. However, on the basis of the WT1 negativity, we believe that HH is better considered as a lymphatic malformation rather than a lymphatic neoplasm.

摘要

背景

钉突状血管瘤 (HH) 目前被归类为良性血管肿瘤,尽管尚不清楚该病变是否向血液或淋巴内皮细胞分化。Wilms 肿瘤 1(WT1)的内皮标志物免疫染色有助于区分血管性肿瘤和畸形,前者呈阳性,后者呈阴性。

目的

我们旨在研究 HH 中 WT1、人疱疹病毒 8 潜伏核抗原、D2-40 和 Ki-67 的免疫表型,以进一步了解其组织发生。

方法

我们评估了德国 Friedrichshafen 的 Dermatohistopathologische Gemeinschaftslabor 收集的 52 例 HH。所有病例均进行 WT1 免疫组化染色。对 52 例病变中的 10 例进行 D2-40 和 Ki-67 染色,12 例病变进行人疱疹病毒 8 潜伏核抗原染色。

结果

所有 52 例 HH 均完全呈 WT1 免疫染色阴性。对 10 例 HH 进行的免疫组化显示,8 例呈弥漫强阳性 D2-40 染色,2 例呈局灶性阳性。所有检测病例均显示 Ki-67 和人疱疹病毒 8 潜伏核抗原染色阴性。

局限性

没有局限性。

结论

尽管 HH 的确切组织发生尚不清楚,但大多数进行的免疫组织化学研究支持淋巴分化。然而,基于 WT1 阴性,我们认为 HH 最好被视为淋巴管畸形而不是淋巴肿瘤。

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