Mediastinal NUT Carcinoma With Raised Serum Alpha-Fetoprotein Mimicking a Malignant Germ Cell Tumor: Suspicion Raised Due to Negative Serum miR-371a-3p Levels.

IF 1.3 4区 医学 Q3 PATHOLOGY
Pediatric and Developmental Pathology Pub Date : 2025-07-01 Epub Date: 2025-04-25 DOI:10.1177/10935266251335391
Sheng-Yuan Kan, Cinzia G Scarpini, Dawn Ward, Ben Fleming, Heok K Cheow, Ibrahim Jalloh, John A Tadross, James Watkins, Thomas Roberts, Jamie Trotman, Patrick Tarpey, Nicholas Coleman, C Elizabeth Hook, Charlotte Burns, Claire Trayers, Matthew J Murray
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引用次数: 0

Abstract

NUT carcinoma is challenging to diagnose and may mimic a germ cell tumor (GCT) due to raised serum alpha-fetoprotein (AFP). A 15-year-old patient presented with back pain and cough. Investigation revealed a mediastinal mass and multiple bone metastases. Serum AFP was highly elevated, consistent with a metastatic malignant nonseminomatous GCT. Aggressive chemotherapy was initiated with initial response, unfortunately not sustained. Diagnostic biopsy showed undifferentiated tumor cells with weak GCT immunophenotype but was ultimately non-diagnostic. Serum miR-371a-3p levels, highly sensitive/specific for malignant GCTs, were negative casting diagnostic suspicion. Routine use of agnostic molecular investigations, including whole genome sequencing, identified a chromosome 15:19 translocation, with BRD4::NUTM1 gene fusion on RNA sequencing, confirming NUT carcinoma. Subsequent NUTM1 immunohistochemistry was positive. A high index of clinical suspicion is required for non-pathologically/molecularly confirmed diagnoses. Serum miR-371a-3p quantification ruled out malignant GCT and routine agnostic molecular studies identified the correct diagnosis; a low threshold for NUTM1 immunohistochemistry is thus recommended.

血清α -胎蛋白升高与恶性生殖细胞肿瘤相似的纵隔NUT癌:血清miR-371a-3p水平阴性引起怀疑
由于血清甲胎蛋白(AFP)升高,NUT癌的诊断具有挑战性,可能与生殖细胞肿瘤(GCT)相似。患者15岁,主要表现为背痛和咳嗽。检查发现纵隔肿块和多发骨转移。血清AFP高度升高,符合转移性恶性非半细胞瘤性GCT。积极的化疗开始有初步反应,不幸的是没有持续。诊断活检显示未分化的肿瘤细胞具有弱GCT免疫表型,但最终无法诊断。血清miR-371a-3p水平,对恶性gct高度敏感/特异性,是阴性的诊断怀疑。常规的分子研究,包括全基因组测序,发现了一个染色体15:19易位,在RNA测序上与BRD4::NUTM1基因融合,证实了NUT癌。后续NUTM1免疫组化阳性。对于非病理/分子确诊的诊断,需要高度的临床怀疑。血清miR-371a-3p定量排除恶性GCT和常规分子诊断鉴别正确诊断;因此建议采用低阈值的NUTM1免疫组织化学检测。
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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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