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ALK 阳性组织细胞增生症:一个扩展的临床病理谱,并且经常存在 KIF5B-ALK 融合。

ALK-positive histiocytosis: an expanded clinicopathologic spectrum and frequent presence of KIF5B-ALK fusion.

机构信息

Department of Pathology and Laboratory Medicine, KK Women's and Children's Hospital, Singapore, Singapore.

Duke-NUS Medical School, Singapore, Singapore.

出版信息

Mod Pathol. 2019 May;32(5):598-608. doi: 10.1038/s41379-018-0168-6. Epub 2018 Dec 20.

Abstract

In 2008, we presented three cases of ALK-positive histiocytosis as a novel systemic histiocytic proliferation of early infancy with hepatosplenomegaly and dramatic hematological disturbances. This series of 10 cases (including the original three cases) describes an expanded clinicopathological spectrum and the molecular findings of this histiocytic proliferation. Six patients had disseminated disease: five presented in early infancy with eventual disease resolution, and the sixth presented at 2 years of age and died of intestinal, bone marrow, and brain involvement. The other four patients had localized disease involving nasal skin, foot, breast, and intracranial cavernous sinus - the first three had no recurrence after surgical resection, while the cavernous sinus lesion showed complete resolution with crizotinib therapy. The lesional histiocytes were very large, with irregularly folded nuclei, fine chromatin, and abundant eosinophilic cytoplasm, sometimes with emperipolesis. There could be an increase in foamy histiocytes and Touton giant cells with time, resembling juvenile xanthogranuloma. Immunostaining showed that the histiocytes were positive for ALK, histiocytic markers (CD68, CD163) and variably S100, while being negative for CD1a, CD207, and BRAF-V600E. Next-generation sequencing-based anchored multiplex PCR (Archer® FusionPlex®) performed in six cases identified KIF5B-ALK gene fusion in five and COL1A2-ALK fusion in one. There was no correlation of gene fusion type with disease localization or dissemination. The clinicopathological spectrum of ALK-positive histiocytosis is broader than originally described, and this entity is characterized by frequent presence of KIF5B-ALK gene fusion. We recommend that every unusual histiocytic proliferative disorder, especially disseminated lesions, be tested for ALK expression because of the potential efficacy of ALK inhibitor therapy in unresectable or disseminated disease.

摘要

2008 年,我们报告了三例 ALK 阳性组织细胞增生症,这是一种新的婴儿早期系统性组织细胞增生症,具有肝脾肿大和明显的血液学紊乱。这一系列 10 例(包括最初的 3 例)描述了这种组织细胞增生的扩展临床病理谱和分子发现。6 例患者患有播散性疾病:5 例在婴儿早期发病,最终疾病缓解,第 6 例在 2 岁时发病,死于肠、骨髓和脑受累。另外 4 例患者患有局限性疾病,累及鼻皮肤、脚、乳房和颅内海绵窦 - 前 3 例患者在手术后无复发,而海绵窦病变在克唑替尼治疗后完全缓解。病变组织细胞非常大,核不规则折叠,染色质精细,嗜酸性细胞质丰富,有时伴有吞噬现象。随着时间的推移,泡沫状组织细胞和 Touton 巨细胞可能会增加,类似于幼年黄色肉芽肿。免疫组化显示组织细胞阳性表达 ALK、组织细胞标志物(CD68、CD163)和不定型 S100,而 CD1a、CD207 和 BRAF-V600E 阴性。对 6 例患者进行的基于下一代测序的锚定多重 PCR(Archer®FusionPlex®)鉴定出 5 例存在 KIF5B-ALK 基因融合,1 例存在 COL1A2-ALK 融合。基因融合类型与疾病定位或播散无相关性。ALK 阳性组织细胞增生症的临床病理谱比最初描述的更广泛,其特征是频繁存在 KIF5B-ALK 基因融合。我们建议,由于 ALK 抑制剂治疗在不可切除或播散性疾病中的潜在疗效,对于每一种不寻常的组织细胞增生性疾病,特别是播散性病变,都应进行 ALK 表达检测。

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