扩大EWSR1::CREM融合瘤的范围:一种罕见的儿童鼻腔粘液瘤。

IF 1.3 4区 医学 Q3 PATHOLOGY Pediatric and Developmental Pathology Pub Date : 2024-01-01 Epub Date: 2023-10-11 DOI:10.1177/10935266231199931
Shamen Koh, Lavisha S Punjabi, Kenneth Tou En Chang, Neville Wei Yang Teo, Constance Ee Hoon Teo, Shui Yen Soh, Henry Kun Kiaang Tan
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引用次数: 0

摘要

EWSR1::CREM基因融合在各种软组织肿瘤中越来越被识别,包括明确的实体,如血管瘤样纤维组织细胞瘤或透明细胞肉瘤,以及其他不可分类的肿瘤。作为一组,EWSR1::CREM融合瘤通常表现为原始梭形或上皮样细胞、黏液样间质和广泛的免疫表型。在此,我们提出了一个不寻常的病例,一名儿童被诊断为鼻内恶性黏液样肿瘤,携带EWSR1::CREM基因融合。据我们所知,这是第一例具有这种特殊融合的鼻腔粘液样肿瘤。讨论了该病例的诊断和管理。
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Expanding the Spectrum of EWSR1::CREM Fusion Tumors: An Unusual Pediatric Intranasal Myxoid Tumor.

EWSR1::CREM gene fusions are increasingly being recognized in a diverse number of soft tissue tumors, including well-defined entities such as angiomatoid fibrous histiocytoma or clear cell sarcoma, and other unclassifiable tumors. As a group, EWSR1::CREM fused tumors often demonstrate primitive spindle or epithelioid cells, myxoid stroma, and a broad immunophenotype. Herein we present an unusual case of a child diagnosed with an intranasal malignant myxoid tumor harboring an EWSR1::CREM gene fusion. To the best of our knowledge, this is the first case of intranasal myxoid tumor with this particular fusion. Diagnosis and management of the case is discussed.

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来源期刊
CiteScore
3.70
自引率
5.30%
发文量
59
审稿时长
6-12 weeks
期刊介绍: The Journal covers the spectrum of disorders of early development (including embryology, placentology, and teratology), gestational and perinatal diseases, and all diseases of childhood. Studies may be in any field of experimental, anatomic, or clinical pathology, including molecular pathology. Case reports are published only if they provide new insights into disease mechanisms or new information.
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