Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Division of Hematology, Department of Medicine, University of Washington, Seattle, Washington, USA.
J Cutan Pathol. 2022 Aug;49(8):727-730. doi: 10.1111/cup.14231. Epub 2022 Apr 5.
Several mutations and gene fusions involved in the mitogen-activated protein kinase (MAPK) pathway have been reported in histiocytic neoplasms including Langerhans cell histiocytosis and non-Langerhans-cell histiocytosis (NLCH). We identified a GAB2::BRAF fusion in a cutaneous lesion from a 22-year-old woman who presented with central diabetes insipidus and red/brown papules on her face, oral mucosa, axilla, and groin. Skin biopsy showed a CD68+, S100-, and CD1a- histiocytic proliferation consistent with NLCH, best clinically classified as xanthoma disseminatum. Next-generation sequencing identified a GAB2::BRAF fusion involving exon 2 of GAB and exon 10 of BRAF. This case implicates a novel fusion in the MAPK signaling pathway, not previously reported in histiocytic neoplasms, as a possible driver of NLCH. Our findings underscore the utility of performing molecular studies on skin biopsy specimens with NLCH to help identify potential targets for therapy.
几种涉及丝裂原活化蛋白激酶(MAPK)途径的突变和基因融合已在组织细胞肿瘤中报道,包括朗格汉斯细胞组织细胞增生症和非朗格汉斯细胞组织细胞增生症(NLCH)。我们在一名 22 岁女性的皮肤病变中鉴定出 GAB2::BRAF 融合,该女性表现为中枢性尿崩症和面部、口腔黏膜、腋窝和腹股沟的红色/棕色丘疹。皮肤活检显示 CD68+、S100-和 CD1a-组织细胞增生,符合 NLCH,临床最佳分类为播散性黄色瘤。下一代测序鉴定出 GAB2::BRAF 融合涉及 GAB 的外显子 2 和 BRAF 的外显子 10。该病例提示 MAPK 信号通路中的一种新融合,以前未在组织细胞肿瘤中报道,可能是 NLCH 的驱动因素。我们的研究结果强调了对具有 NLCH 的皮肤活检标本进行分子研究的实用性,以帮助确定治疗的潜在靶点。