表皮生长因子受体(EGFR)突变的子宫颈 S100 和 CD34 阳性纺锤形细胞瘤:一种迄今未被发现的表型和表观遗传学上与子宫 "NTRK 重组纺锤形细胞瘤 "重叠的肿瘤。

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2024-10-10 DOI:10.1007/s00428-024-03936-z
Michael Michal, Josef Kuruc, Veronika Hájková, Květoslava Michalová, Natálie Klubíčková
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引用次数: 0

摘要

NTRK重排纺锤形细胞瘤是最新第五版世界卫生组织软组织和女性生殖器肿瘤分类中新出现的一种肿瘤。通过免疫组化,它们通常对 CD34、S100 蛋白和 CD30 呈阳性反应,并通常携带激酶基因融合,如 NTRK1/2/3、RET 和 BRAF。在妇科领域,它们通常影响子宫颈或子宫体。大多数报道的病例具有纤维肉瘤样形态,偶尔表现为血管周围和基质透明化,只有少数病例表现为细胞较少的纺锤形细胞增生。除一例有 RET 融合外,其他所有妇科病例均为 NTRK1/2/3 融合。除了激酶基因融合外,软组织中的类似肿瘤也可能携带活化的表皮生长因子受体(EGFR)或BRAF点突变,但在子宫中还没有此类病例。在此,我们报告两例来自子宫颈的病例,这两例病例的形态和分子特征以前在这一解剖部位从未报道过。这两名患者分别为 46 岁和 34 岁,临床表现为宫颈息肉,直径均为 8 毫米。从组织学上看,两例患者的息肉均呈圆形,由缺乏有丝分裂活性的平滑纺锤形细胞增生而成,生长在纤维化基质中,基质中点缀着突出的小血管,血管壁很厚,呈透明状。免疫组化结果显示,两个病例均弥漫表达 CD34、CD30 和 S100 蛋白,而 SOX10 阴性。两个病例都有表皮生长因子受体 20 外显子突变,但没有发现任何融合或明显的拷贝数变化。病例1的患者接受了子宫切除术和输卵管切除术,未发现其他残留肿瘤,确诊后27个月仍健在。病例 2 的患者在确诊时没有其他已知肿瘤,但没有后续资料。我们认为,所报告的病例代表了一种迄今为止尚未认识到的带有新型表皮生长因子受体突变的子宫颈 "NTRK重排纺锤形细胞瘤 "变体。
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S100 and CD34 positive spindle cell tumors of the uterine cervix with EGFR mutation: a hitherto unrecognized neoplasm phenotypically and epigenetically overlapping with "NTRK-rearranged spindle cell neoplasms" of the uterus.

NTRK-rearranged spindle cell neoplasm represents an emerging entity included in the latest 5th edition of WHO classification of both soft tissue and female genital tumors. By immunohistochemistry, they are commonly positive for CD34, S100 protein, and CD30 and typically harbor fusions of kinase genes such as NTRK1/2/3, RET, and BRAF. In the gynecological tract, they typically affect the uterine cervix or uterine body. Most of the reported cases had fibrosarcoma-like morphology, occasionally showing perivascular and stromal hyalinization with only a few cases showing a less cellular spindle cell proliferation. Except for one case with RET fusion, all other gynecological cases harbored exclusively NTRK1/2/3 fusions. Besides kinase gene fusions, the analogous tumors in soft tissues may also harbor activating EGFR or BRAF point mutations, but no such case has been described in the uterus. Herein we are reporting two cases from the uterine cervix showing morphology and molecular features previously unreported at this anatomic site. The patients were 46 and 34 years old and clinically presented with unremarkable cervical polyps each measuring 8 mm in diameter. Histologically, both cases had a rounded polypoid outline and were composed of hypocellular proliferation of bland spindle cells lacking mitotic activity and growing in a fibrotic stroma which was punctuated by prominent small vessels with thick hyalinized walls. Immunohistochemically, both showed a diffuse expression of CD34, CD30, and S100 protein, whereas SOX10 was negative. Both cases harbored exon 20 EGFR mutation and did not reveal any fusions or significant copy number changes. The patient in case 1 was treated by hysterectomy with salpingectomy with no other residual tumor detected, and she was alive and well 27 months after the diagnosis. The patient in case 2 had no other known tumors at the time of diagnosis, but no follow-up is available. We believe the reported cases represent a hitherto unrecognized variant of "NTRK-rearranged spindle cell neoplasms" of the uterine cervix with novel EGFR mutations.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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