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上皮样细胞组织细胞瘤的梭形细胞变异型(梭形细胞组织细胞瘤)伴有 ALK 基因融合:病例系列和文献复习。

Spindle cell variant of epithelioid cell histiocytoma (spindle cell histiocytoma) with ALK gene fusions: Cases series and review of the literature.

机构信息

Department of Dermatopathology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Department of Dermatology, The Johns Hopkins School of Medicine, Baltimore, Maryland, USA.

出版信息

J Cutan Pathol. 2021 Jul;48(7):837-841. doi: 10.1111/cup.13923. Epub 2020 Dec 11.

DOI:10.1111/cup.13923
PMID:33217002
Abstract

BACKGROUND

Epithelioid fibrous histiocytoma (EFH) is an uncommon dermal neoplasm expressing anaplastic lymphoma kinase (ALK) protein. Rarely a histopathological variant of this entity exhibits exclusively spindle cells. We report three cases of EFH that do not completely fulfill phenotypic criteria featuring spindle cell morphology and expressing ALK protein. We also analyze the fusion partner genes rearranged with ALK in these cases.

METHODS

ALK expression and rearrangement status were evaluated by immunohistochemistry (IHC), fluorescence in situ hybridization (FISH), and next generation sequencing based gene fusion analysis.

RESULTS

Three cases, all from females between 25 and 55 years old, have been biopsied from back, left arm, and thumb. All three cases showed tumor with exclusively spindle cell morphology without any epithelioid cells. The tumor cells exhibited strong ALK expression by IHC and FISH study confirmed ALK gene rearrangement in all three cases. DCTN1-ALK fusion was identified in two cases.

CONCLUSION

EFH is not always purely epithelioid and its spindled cell variant, spindle cell histiocytoma, should be included in the differential diagnosis of superficial dermal spindled cell neoplasms. ALK immunostain is a useful diagnostic marker for this entity and further studies may be useful to investigate whether DCTN1-ALK fusion mutations are specific to EFH with spindled cell features.

摘要

背景

上皮样纤维组织细胞瘤(EFH)是一种罕见的真皮肿瘤,表达间变性淋巴瘤激酶(ALK)蛋白。这种实体的罕见组织病理学变体仅表现为梭形细胞。我们报告了三例 EFH 病例,这些病例不完全符合具有梭形细胞形态和表达 ALK 蛋白的表型标准。我们还分析了这些病例中与 ALK 重排的融合伙伴基因。

方法

通过免疫组织化学(IHC)、荧光原位杂交(FISH)和基于下一代测序的基因融合分析评估 ALK 表达和重排状态。

结果

三例均为女性,年龄在 25 至 55 岁之间,分别来自背部、左臂和拇指。所有三例均表现为仅具有梭形细胞形态的肿瘤,无任何上皮样细胞。IHC 显示肿瘤细胞强烈表达 ALK,FISH 研究证实所有三例均存在 ALK 基因重排。在两例中鉴定出 DCTN1-ALK 融合。

结论

EFH 并不总是纯粹上皮样的,其梭形细胞变体,梭形细胞组织细胞瘤,应包括在真皮浅层梭形细胞肿瘤的鉴别诊断中。ALK 免疫染色是该实体的有用诊断标志物,进一步的研究可能有助于研究 DCTN1-ALK 融合突变是否特异性地存在于具有梭形细胞特征的 EFH 中。

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Spindle cell variant of epithelioid cell histiocytoma (spindle cell histiocytoma) with ALK gene fusions: Cases series and review of the literature.上皮样细胞组织细胞瘤的梭形细胞变异型(梭形细胞组织细胞瘤)伴有 ALK 基因融合:病例系列和文献复习。
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