Children's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.
Department of Pediatrics, Shiga University of Medical Science, Seta Tsukinowa-cho, Otsu, Shiga, 520-2192, Japan.
Int J Hematol. 2023 Jul;118(1):119-124. doi: 10.1007/s12185-023-03588-w. Epub 2023 Apr 3.
Langerhans cell histiocytosis-associated neurodegenerative disease (LCH-ND) is the most serious late complication secondary to LCH and is gradually progressive, destructive, and irreversible. Detection of the BRAF V600E mutation in peripheral blood mononuclear cells (PBMCs), even in the absence of active LCH lesions, is considered a sign of clinical LCH-ND, presenting with both abnormal imaging findings and neurological symptoms. However, the detection of the BRAF V600E mutation in PBMCs of patients with asymptomatic radiological LCH-ND (rLCH-ND) without active LCH lesions who present only with abnormal imaging findings is unknown. In this study, we analyzed the BRAF V600E mutations in PBMCs and cell-free DNA (cfDNA) of patients with rLCH-ND without active LCH lesions (n = 5) using a droplet digital polymerase chain reaction (ddPCR) assay. The BRAF V600E mutation in PBMCs was detected in three out of five (60%) cases. The mutant allele frequencies in the three positive cases were 0.049%, 0.027%, and 0.015%, respectively. However, the cfDNA BRAF V600E mutation remained undetected in all patients. Detection of the BRAF V600E mutant allele in PBMCs may be helpful in identifying asymptomatic rLCH-ND in patients at high risk for developing LCH-ND, including those with relapses at CNS risk sites or central diabetes insipidus.
朗格汉斯细胞组织细胞增生症相关神经退行性疾病(LCH-ND)是 LCH 继发的最严重的晚期并发症,呈进行性、破坏性和不可逆性进展。在外周血单个核细胞(PBMC)中检测到 BRAF V600E 突变,即使没有活动性 LCH 病变,也被认为是临床 LCH-ND 的标志,表现为影像学异常和神经症状。然而,对于无症状影像学 LCH-ND(rLCH-ND)且无活动性 LCH 病变的患者,仅表现为影像学异常,其 PBMC 中 BRAF V600E 突变的检测情况尚不清楚。在这项研究中,我们使用液滴数字聚合酶链反应(ddPCR)检测了 5 例无活动性 LCH 病变的 rLCH-ND 患者的 PBMC 和游离细胞 DNA(cfDNA)中的 BRAF V600E 突变。在 5 例患者中,有 3 例(60%)检测到 PBMC 中的 BRAF V600E 突变。在 3 例阳性病例中,突变等位基因频率分别为 0.049%、0.027%和 0.015%。然而,所有患者的 cfDNA BRAF V600E 突变均未检测到。在 PBMC 中检测到 BRAF V600E 突变等位基因可能有助于识别高危 LCH-ND 患者中的无症状 rLCH-ND,包括 CNS 危险部位复发或中枢性尿崩症患者。