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胸段SMARCA4缺陷型未分化肿瘤:小组织样本中的诊断挑战及误诊可能性

Thoracic SMARCA4-deficient undifferentiated tumour: Diagnostic challenges and potential for misdiagnosis in small tissue samples.

作者信息

Maartens Deborah Johanna, Moolla Muhammad Saadiq, Ndaba Sibusiso, Vlok Sucari Susanna Catherina, Hendricks Firzana, Koegelenberg Coenraad Frederik Nicolaas, van Wyk Abraham Christoffel

机构信息

Division of Anatomical Pathology, Tygerberg Hospital, National Health Laboratory Service, Faculty of Medicine and Health Sciences Stellenbosch University Cape Town South Africa.

Division of Pulmonology, Department of Medicine, Faculty of Medicine and Health Sciences Stellenbosch University and Tygerberg Hospital Cape Town South Africa.

出版信息

Respirol Case Rep. 2023 Oct 26;11(11):e01238. doi: 10.1002/rcr2.1238. eCollection 2023 Nov.

Abstract

We report a diagnostically challenging case of a SMARCA4-deficient undifferentiated tumour to emphasize its potential to mimic other malignant tumours on histology, especially in small biopsies and where rhabdoid morphology is lacking. A 48-year-old man, who was known for chronic obstructive pulmonary disease and polysubstance use, presented with dyspnoea and an anterior mediastinal mass that had grown rapidly over a seven-month period. The rapid growth and location in the anterior mediastinum raised clinical suspicion for lymphoma or a germ cell tumour. Microscopic examination of a transthoracic, ultrasound-guided, core needle biopsy revealed relatively uniform, malignant epithelioid cells with clear cytoplasm, but lacking any rhabdoid features. Tumour necrosis was prominent. The immunohistochemistry panel was negative for lymphoma markers, but positive for SALL4 (a marker typically associated with germ cell tumours), CD34, EMA, and HepPar1, while expression of SMARCA4 and claudin-4 was entirely lost. Only focal cytokeratin expression was demonstrated. SMARCB1 (INI1) expression was retained. The diagnosis of SMARCA4-DUT was made based on these findings. Unfortunately, the tumour was already at an advanced stage at diagnosis (stage IVA) and the patient had a poor performance status. He was treated with palliative radiotherapy with no significant improvement in performance status and passed away 3 months after diagnosis. The case highlights the importance of considering SMARCA4-DUT in the differential diagnosis of an undifferentiated, rapidly growing thoracic tumour and the potential for misdiagnosis on a small tissue sample, particularly as rhabdoid morphology may be absent.

摘要

我们报告了一例诊断具有挑战性的SMARCA4缺陷型未分化肿瘤病例,以强调其在组织学上可能模仿其他恶性肿瘤,特别是在小活检标本中且缺乏横纹肌样形态的情况下。一名48岁男性,因慢性阻塞性肺疾病和多种物质使用而闻名,出现呼吸困难和前纵隔肿块,该肿块在7个月内迅速生长。前纵隔的快速生长和位置引起了对淋巴瘤或生殖细胞肿瘤的临床怀疑。经胸超声引导下的粗针活检显微镜检查显示,肿瘤细胞相对均匀,为恶性上皮样细胞,胞质清晰,但无任何横纹肌样特征。肿瘤坏死明显。免疫组化结果显示淋巴瘤标志物为阴性,但SALL4(一种通常与生殖细胞肿瘤相关的标志物)、CD34、EMA和HepPar1为阳性,而SMARCA4和claudin-4的表达完全缺失。仅显示局灶性细胞角蛋白表达。SMARCB1(INI1)表达保留。基于这些发现做出了SMARCA4缺陷型未分化肿瘤的诊断。不幸的是,诊断时肿瘤已处于晚期(IVA期),患者的体能状态较差。他接受了姑息性放疗,但体能状态没有明显改善,诊断后3个月去世。该病例强调了在未分化、快速生长的胸部肿瘤鉴别诊断中考虑SMARCA4缺陷型未分化肿瘤的重要性,以及在小组织样本上可能误诊的可能性,特别是当缺乏横纹肌样形态时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb02/10603309/be119b57ff92/RCR2-11-e01238-g002.jpg

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