伴有EWSR1::CREM融合的颅内间充质肿瘤引起的全身性炎症与IL-6/STAT3信号相关。

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY
Neuropathology Pub Date : 2023-06-01 DOI:10.1111/neup.12877
Keishiro Hojo, Takuya Furuta, Satoru Komaki, Yukako Yoshikane, Jin Kikuchi, Hideo Nakamura, Mizuki Ide, Saho Shima, Yusuke Hiyoshi, Junichiro Araki, Seiji Tanaka, Shuichi Ozono, Akihiko Yoshida, Sumihito Nobusawa, Motohiro Morioka, Ryuta Nishikomori
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引用次数: 1

摘要

儿童肿瘤疾病约占不明原因发热(FUO)病例的10%,大多数肿瘤疾病是白血病、淋巴瘤和神经母细胞瘤。虽然颅咽管瘤、转移性脑瘤和Castleman病已被报道,但脑肿瘤很少被报道为引起FUO的原因。我们报告一例具有FET:CREB融合基因的颅内间充质瘤(IMT),其炎症表型无神经症状。一名10岁女孩因2个月的间歇性发热和头痛病史入院,但其既往病史及家族史均无特殊事件。脓毒症检查未见病理组织,经验性抗生素治疗无效。骨髓检查呈阴性。脑脊液检查显示蛋白质和细胞计数升高,头部磁共振成像显示左小脑半球血管增生肿块,对比增强。患者行肿瘤切除术,间歇性发热消失。病理检查与典型的血管瘤样纤维组织细胞瘤(AFH)相似,但形态特征与AFH黏液样变体不同;然后进行分离荧光原位杂交,证实肿瘤含有罕见的EWSR1::CREM融合基因(Ewing肉瘤断点区1基因(EWSR1)和cAMP反应元件结合(CREB)家族基因)。因此,我们诊断为伴有EWSR1::CREM融合的IMT。肿瘤切除后血清白细胞介素6 (IL-6)浓度升高正常,提示发热可能由肿瘤源性IL-6引起。这是第一例伴有EWSR1::CREM融合的IMT,并表现出与IL-6/信号转导和转录激活因子3 (STAT3)信号通路相关的副肿瘤症状。虽然脑肿瘤很少被诊断为引起FUO的原因,但即使在没有异常神经学发现的情况下,也应将其视为不明原因发热的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Systemic inflammation caused by an intracranial mesenchymal tumor with a EWSR1::CREM fusion presenting associated with IL-6/STAT3 signaling.

Pediatric neoplastic diseases account for about 10% of cases of fever of unknown origin (FUO), and most neoplastic disease cases are leukemia, lymphoma, and neuroblastoma. Brain tumors are rarely reported as the cause of FUO, although craniopharyngioma, metastatic brain tumor, and Castleman's disease have been reported. We report a case of intracranial mesenchymal tumor (IMT) with a FET:CREB fusion gene, which had inflammatory phenotype without neurological signs. A 10-year-old girl was admitted with a 2-month history of intermittent fever and headache, whereas her past history as well as her family history lacked special events. Sepsis work-up showed no pathological organism, and empirical antibiotic therapy was not effective. Bone marrow examination showed a negative result. Cerebrospinal fluid examination showed elevated protein as well as cell counts, and head magnaetic resonance imaging showed a hypervascular mass lesion with contrast enhancement in the left cerebellar hemisphere. The patient underwent tumor excision, which made the intermittent fever disappear. Pathological examinations resembled those of classic angiomatoid fibrous histiocytoma (AFH), but the morphological features were distinct from the AFH myxoid variant; then we performed break-apart fluorescence in situ hybridization and confirmed the tumor harbored the rare EWSR1::CREM fusion gene (Ewing sarcoma breakpoint region 1 gene (EWSR1) and cAMP response element binding (CREB) family gene). Consequently, we diagnosed the condition as IMT with EWSR1::CREM fusion. Elevated serum concentration of interleukin 6 (IL-6) was normalized after tumor resection, which suggested the fever could be caused by tumor-derived IL-6. This is the first case of IMT with EWSR1::CREM fusion that showed paraneoplastic symptoms associated with the IL-6/signal transducer and activator of transcription 3 (STAT3) signaling pathway. Although brain tumors are rarely diagnosed as a responsible disease for FUO, they should be considered as a cause of unknown fever even in the absence of abnormal neurological findings.

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来源期刊
Neuropathology
Neuropathology 医学-病理学
CiteScore
4.10
自引率
4.30%
发文量
105
审稿时长
6-12 weeks
期刊介绍: Neuropathology is an international journal sponsored by the Japanese Society of Neuropathology and publishes peer-reviewed original papers dealing with all aspects of human and experimental neuropathology and related fields of research. The Journal aims to promote the international exchange of results and encourages authors from all countries to submit papers in the following categories: Original Articles, Case Reports, Short Communications, Occasional Reviews, Editorials and Letters to the Editor. All articles are peer-reviewed by at least two researchers expert in the field of the submitted paper.
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