Atypical clear cell sarcoma of the pleura presenting as large pleural effusion with 22q12 abnormality: A challenging case with twists and turns

Xiaoming Zhang , Paul J. Zhang , Robyn Sussman , Leslie A. Litzky , John C. Kucharczuk , Charuhas Deshpande
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引用次数: 1

Abstract

Primary clear cell sarcoma of soft tissue (CCSST) arising from the pleura is an infrequent occurrence, with only two cases reported in the English literature. We report a rare case of pleural CCSST with unusual clinical features and unconventional morphology. A 68-year-old man presented with a large right pleural effusion that developed following a dental abscess. He was treated with thoracentesis and antibiotics for suspected empyema without significant improvement. A CT-guided biopsy was performed and showed a malignant epithelioid neoplasm with significant pleomorphism and melanocytic differentiation, highly suggestive of a melanoma. The diagnosis was subsequently amended to CCSST based on the combined genetic findings (i.e., chromosome 22 abnormality, microsatellite stable status, no evidence of ultraviolet mutational signature, and lack of BRAF or any other mutations commonly identified in melanoma). Apart from the peculiar location, the present case showed several atypical features, such as older age at onset, unusual clinical presentations mimicking an infection, and unconventional morphology with significant pleomorphism and brisk mitotic activity. As such, it may be better classified as atypical CCSST. This case highlights the challenges in diagnosing CCSST and emphasizes the importance of including CCSST in the differential diagnosis of an epithelioid tumor with melanocytic differentiation.

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非典型胸膜透明细胞肉瘤表现为22q12异常的大胸腔积液:一个具有挑战性的曲折病例
起源于胸膜的软组织透明细胞肉瘤(CCSST)是一种罕见的病例,在英文文献中仅报道了两例。我们报告一例罕见的胸膜CCSST,其临床特征和形态不同寻常。一个68岁的男人提出了一个大的右侧胸腔积液,发展后牙脓肿。患者因疑似脓胸接受胸腔穿刺和抗生素治疗,无明显改善。ct引导下活检显示为恶性上皮样肿瘤,具有明显的多形性和黑素细胞分化,高度提示黑色素瘤。随后,根据综合遗传发现(即22号染色体异常、微卫星稳定状态、无紫外线突变特征证据、缺乏BRAF或黑色素瘤中常见的任何其他突变),将诊断修改为CCSST。除了特殊的位置外,本病例还表现出一些非典型特征,如发病年龄较大,临床表现异常,类似感染,形态异常,具有明显的多形性和活跃的有丝分裂活性。因此,它可能更好地归类为非典型CCSST。本病例强调了诊断CCSST的挑战,并强调了在黑色素细胞分化的上皮样肿瘤鉴别诊断中包括CCSST的重要性。
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来源期刊
Human Pathology: Case Reports
Human Pathology: Case Reports Medicine-Pathology and Forensic Medicine
CiteScore
0.50
自引率
0.00%
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0
审稿时长
16 weeks
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