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乳腺恶性叶状肿瘤伴骨肉瘤及软骨肉瘤为主的分化:1例罕见病例报告并文献复习

Malignant phyllodes tumor of the breast with predominant osteosarcoma and chondrosarcomatous differentiation: a rare case report and review of literature.

作者信息

Li Wenfang, Ou Qin, Li Yingdong, Yuan Linlin Yuan

机构信息

Taihe Hospital, Hubei University of Medicine, Shiyan, China.

Department of Pathology, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan, Hebei, China.

出版信息

Front Oncol. 2024 Apr 19;14:1372710. doi: 10.3389/fonc.2024.1372710. eCollection 2024.

DOI:10.3389/fonc.2024.1372710
PMID:38706594
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11066275/
Abstract

BACKGROUND

Phyllodes tumors (PTs), which account for less than 1% of mammary gland tumors, composed of both epithelial and stromal components. If a malignant heterologous component is encountered, PT is considered malignant. Malignant phyllodes tumors (MPTs) only account for 8% to 20% of PTs. We report a case of MPT with osteosarcoma and chondrosarcoma differentiation and review the literature to discuss the differential diagnosis and therapy.

CASE PRESENTATION

A 59-year-old Chinese woman come to our hospital because of a palpable mass she had had for 1 months in the left breast. Preoperative core needle biopsy (CNB) was performed on the left breast mass on January 11, 2023. Pathological diagnosis was malignant tumor, the specific type was not clear. Mastectomy and sentinel lymph node biopsy of the left breast was performed. No metastasis was found in 3 sentinel lymph nodes identified by carbon nanoparticles and methylene blue double staining. Heterologous osteosarcoma and chondrosarcomatous differentiation of phyllodes tumor were observed. Immunohistochemistry: spindle tumor cells ER(-), PR(-), HER-2(-), CK-pan(-), CK7(-), CK8(-), SOX10(-), S100(-), and MDM2(-), CK5/6(-), P63(-), P40(-) were all negative. CD34:(+), SATB2(+), P53(90% strong), CD68 (+), Ki-67(LI: about 60%). No ductal carcinoma was found in the breast. Fluorescence hybridization (FISH) indicated USP6 was negatively expressed on formalin-fixed, paraffin-embedded (FFPE) tissue sections.

CONCLUSION

MPTs are rare, and heterologous differentiation in MPTs is exceedingly rare. It could be diagnosed by pathology when metaplastic carcinoma, primary osteosarcoma, or myositis ossificans were excluded. This case could help clinicians to improve the prognosis and treatment of this disease.

摘要

背景

叶状肿瘤(PTs)占乳腺肿瘤的比例不到1%,由上皮和间质成分组成。如果遇到恶性异源性成分,则PT被认为是恶性的。恶性叶状肿瘤(MPTs)仅占PTs的8%至20%。我们报告一例具有骨肉瘤和软骨肉瘤分化的MPT病例,并复习文献以讨论鉴别诊断和治疗。

病例介绍

一名59岁中国女性因左侧乳房可触及肿块1个月前来我院就诊。2023年1月11日对左侧乳房肿块进行了术前粗针穿刺活检(CNB)。病理诊断为恶性肿瘤,具体类型不明。进行了左侧乳房切除术和前哨淋巴结活检。经碳纳米颗粒和亚甲蓝双重染色鉴定的3枚前哨淋巴结均未发现转移。观察到叶状肿瘤的异源性骨肉瘤和软骨肉瘤分化。免疫组化:梭形肿瘤细胞雌激素受体(ER)(-)、孕激素受体(PR)(-)、人表皮生长因子受体2(HER-2)(-)、广谱细胞角蛋白(CK-pan)(-)、细胞角蛋白7(CK7)(-)、细胞角蛋白8(CK8)(-)、性别决定区Y框蛋白10(SOX10)(-)、S100蛋白(-)、鼠双微体蛋白2(MDM2)(-)、细胞角蛋白5/6(CK5/6)(-)、p63(-)、p40(-)均为阴性。CD34:(+)、SATB2(+)、P53(90%强阳性)、CD68(+)、Ki-67(标记指数:约60%)。乳房未发现导管癌。荧光原位杂交(FISH)显示在福尔马林固定、石蜡包埋(FFPE)组织切片上USP6呈阴性表达。

结论

MPTs罕见,MPTs中的异源性分化极其罕见。当排除化生性癌、原发性骨肉瘤或骨化性肌炎时,可通过病理诊断。该病例有助于临床医生改善对该疾病的预后和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/11066275/412ac3f968f1/fonc-14-1372710-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/11066275/c8abd16c598d/fonc-14-1372710-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/11066275/cd11268adaca/fonc-14-1372710-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/11066275/412ac3f968f1/fonc-14-1372710-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/11066275/c8abd16c598d/fonc-14-1372710-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/11066275/cd11268adaca/fonc-14-1372710-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/11066275/412ac3f968f1/fonc-14-1372710-g003.jpg

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本文引用的文献

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Metaplastic breast carcinoma: Analysis of clinical and pathologic features, a five-year study.化生性乳腺癌:临床与病理特征分析,一项五年研究。
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Organoid models derived from patients with malignant phyllodes tumor of the breast.源自乳腺恶性叶状肿瘤患者的类器官模型。
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