[细胞角蛋白(pan)阳性EWSR1/FUS::CREB融合腹腔恶性肿瘤:4例临床病理及分子分析]。

Q3 Medicine
F L Zang, Y Wang, X Y Wei, Y L Wang, Y Luo, Y H Guo, T T Ding
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引用次数: 0

摘要

目的:探讨CKpan细胞角蛋白(pan cytokeratin, CKpan)阳性EWSR1/FUS::CREB融合腹腔恶性肿瘤的临床病理及分子遗传学特征。方法:选择2019年1月至2024年7月天津医科大学肿瘤医院病毒科4例ck潘阳性EWSR1/FUS::CREB融合的恶性肿瘤。观察其临床、病理及免疫组织化学特征。利用荧光原位杂交(FISH)和下一代测序(NGS)分析了它们的分子遗传特征。结果:4例患者中男性2例,女性2例,年龄分别为44岁、44岁、48岁和66岁。肿瘤部位1例位于胃与横结肠之间,1例位于胃壁浆液面,1例位于横结肠系膜,1例位于横结肠系膜与小肠系膜。临床表现以腹胀、腹痛为主。手术切除标本中肿瘤最大直径为3.5-8.5 cm。肿瘤切面灰白色、灰黄色,稠度中等。镜下肿瘤细胞主要由上皮样肿瘤细胞组成,2例肿瘤细胞呈实片状或多结节状排列,肿瘤细胞胞质丰富,染色浅,边界不清,伴囊状或微囊状形成,见淋巴细胞和浆细胞套。1例可见假乳头状排列,肿瘤细胞沿纤维血管轴呈放射状分布。另一例呈假腺泡状排列,巢被细长的网状纤维包围。免疫组化显示肿瘤细胞表达CKpan(4/4)和WT1(4/4),其中1例局灶阳性。Vimentin、CK8/18、D2-40、S-100表达强度不同,Calretinin局部表达阳性或阴性。FISH显示EWSR1分离2例,FUS分离2例。NGS分别证实EWSR1::CREM融合(1例)和FUS::CREM融合(2例)。除1例新近确诊外,随访3例:1例因肿瘤复发转移死亡(总生存期33个月),2例存活(1例术后58个月复发,1例术后无复发转移)。结论:ckpan阳性EWSR1/FUS::CREB融合恶性肿瘤是一种罕见的恶性肿瘤,分类不详,多发生于腹腔,常累及胃肠道。FISH和NGS等分子检测有助于明确诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Cytokeratin (pan)-positive EWSR1/FUS::CREB fusion malignant tumor in abdominopelvic cavity: a clinicopathological and molecular analysis of four cases].

Objective: To investigate the clinicopathological and molecular genetic characteristics of pan cytokeratin (CKpan)-positive EWSR1/FUS::CREB fusion malignant tumors in abdominopelvic cavity. Methods: Four cases of malignant tumor with CKpan-positive EWSR1/FUS::CREB fusion were selected from January 2019 to July 2024 in the Department of Pathology, Tianjin Medical University Cancer Hospital, Tianjin, China. Their clinical, pathological, and immunohistochemical characteristics were examined. Their molecular genetic characteristics were analyzed using fluorescence in situ hybridization (FISH) and next-generation sequencing (NGS). Results: Among the 4 patients, there were 2 males and 2 females, aged 44, 44, 48 and 66 years, respectively. The tumor sites included 1 case located between the stomach and transverse colon, 1 case on the serous surface of the gastric wall, 1 case in the transverse mesocolon, and 1 case in transverse mesocolon and small mesentery. The clinical manifestations were mostly abdominal distension and abdominal pain. The maximum diameter of the tumor in the surgical resection specimen was 3.5-8.5 cm. The tumor's cut surface was grayish-white and gray-yellow in color, with medium consistency. Microscopically, the tumor cells were mainly composed of epithelioid tumor cells, and 2 of the tumors showed that tumor cells arranged in a solid sheet or multinodular pattern, and the cytoplasm of the tumor cells was abundant, lightly stained, and the boundaries were unclear, accompanied by the formation of capsules or microcapsules, and lymphocyte and plasma cell sleeves were seen. In one case, the pseudopapillary arrangement was present, and the tumor cells were radially distributed around the fibrovascular axis. In another case, it was arranged in a pseudoacinar pattern, and the nest was surrounded by slender reticular fibers. Immunohistochemistry showed that tumor cells expressed CKpan (4/4) and WT1 (4/4, including 1 focal positive). Vimentin, CK8/18, D2-40 and S-100 were expressed in various intensities, while Calretinin was locally positive or negative. FISH showed that 2 cases had EWSR1 break-apart and 2 cases had FUS break-apart. NGS confirmed the presence of EWSR1::CREM fusion (1 case) and FUS::CREM fusion (2 cases), respectively. Except for 1 recently diagnosed case, 3 cases were followed up: 1 patient died due to tumor recurrence and metastasis (overall survival was 33 months), and 2 patients survived (1 case had recurrence 58 months after surgery, and 1 case had no recurrence or metastasis after surgery). Conclusions: CKpan-positive EWSR1/FUS::CREB fusion malignant tumor is a rare malignancy tumor with undetermined classification that tends to occur in the abdominopelvic cavity and often involves the gastrointestinal tract. Molecular testing such as FISH and NGS is helpful for a definitive diagnosis.

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中华病理学杂志
中华病理学杂志 Medicine-Medicine (all)
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