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一例罕见的乳腺原发性软骨肉瘤:病例报告及文献综述

A Rare Case of Primary Chondrosarcoma of the Breast: A Case Report and Comprehensive Literature Review.

作者信息

Agrawal Sujata, Chowdhury Zachariah, Paul Paramita, Mandal Tanima

机构信息

Department of Oncopathology, Homi Bhabha Cancer Hospital (HBCH) and Mahamana Pandit Madan Mohan Malviya Cancer Centre (MPMMCC), Tata Memorial Centre, Homi Bhabha National Institute (HBNI), Varanasi, India.

出版信息

Discoveries (Craiova). 2024 Sep 30;12(3):e193. doi: 10.15190/d.2024.12. eCollection 2024 Jul-Sep.

Abstract

Breast sarcomas are a diverse group of malignant neoplasms originating from the mammary stroma. They are uncommon tumors, often occurring as a component of other tumors. Among malignant breast mesenchymal tumors, pure sarcomas lacking epithelial components are even rarer, comprising only 0.5% of breast tumors. The most common types include angiosarcomas, liposarcomas, and osteosarcomas. Pure, primary, and de novo chondrosarcomas are exceedingly rare within breast sarcomas, with very few cases reported. Distinguishing them from metaplastic carcinoma and phyllodes tumors with chondromatous areas entails extensive sampling to exclude proliferating ductal elements. Herein, we present a case of primary chondrosarcoma of the breast in a 72-year-old Indian woman. Initial core biopsy suggested a primary chondroid neoplasm or a heterologous component of a phyllodes tumor. The patient underwent modified radical mastectomy, and histological examination confirmed chondrosarcoma, grade 1, after thorough sampling.Clinical Relevance: This case emphasizes the necessity of incorporating rare sarcomatous breast tumors into the differential diagnosis for breast masses, especially those with chondroid differentiation. The report also reinforces the pivotal role of accurate histopathological evaluation in guiding appropriate surgical and adjunctive treatment, which can significantly impact prognosis in such rare malignancies.

摘要

乳腺肉瘤是一组起源于乳腺间质的恶性肿瘤。它们是罕见的肿瘤,常作为其他肿瘤的组成部分出现。在乳腺恶性间叶性肿瘤中,缺乏上皮成分的纯肉瘤更为罕见,仅占乳腺肿瘤的0.5%。最常见的类型包括血管肉瘤、脂肪肉瘤和骨肉瘤。纯的、原发性的和新发的软骨肉瘤在乳腺肉瘤中极其罕见,报道的病例很少。将它们与具有软骨样区域的化生性癌和叶状肿瘤区分开来需要广泛取材以排除增生的导管成分。在此,我们报告一例72岁印度女性的原发性乳腺软骨肉瘤病例。最初的粗针活检提示原发性软骨样肿瘤或叶状肿瘤的异源性成分。患者接受了改良根治性乳房切除术,经全面取材后组织学检查确诊为1级软骨肉瘤。临床意义:该病例强调了将罕见的乳腺肉瘤性肿瘤纳入乳腺肿块鉴别诊断的必要性,尤其是那些具有软骨样分化的肿块。该报告还强化了准确的组织病理学评估在指导适当的手术和辅助治疗中的关键作用,这对这类罕见恶性肿瘤的预后有显著影响。

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