From Fibroadenoma to Phyllodes Tumor: Case Analysis of Borderline and Giant Breast Tumors with Literature Review.

Q3 Medicine
Acta Medica Lituanica Pub Date : 2025-01-01 Epub Date: 2025-02-18 DOI:10.15388/Amed.2025.32.1.4
Justė Kazlauskaitė, Iryna Schmeil
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引用次数: 0

Abstract

Background: Phyllodes tumors are highly uncommon fibroepithelial neoplasms of the breast, accounting for less than 1% of all breast tumors. Differential diagnosis between phyllodes tumors and fibroadenomas by using imaging techniques such as ultrasound or mammography, as well as histological methods, can be challenging due to overlapping features. Phyllodes tumors are categorized into benign, borderline, and malignant types, each posing a different risk of recurrence and metastasis. Despite many advances in the imaging and biopsy techniques, diagnosing phyllodes tumors remains challenging. The purpose of this study is to review the existing literature on this topic and describe two cases of misdiagnosed phyllodes tumors.

Materials and methods: A literature review was conducted by using the Medline (PubMed) database over 10 years. Information concerning the patients was sourced from the Uster Hospital database. After analyzing the cases of women with breast lumps from 2020 to 2023 in the Uster Hospital database, two cases of misdiagnosed phyllodes tumors were identified. These two cases were analyzed retrospectively.

Results: A retrospective study of two cases confirms that phyllodes tumors are a rare phenomenon. A 51-year-old premenopausal woman presented with an 8 × 4 × 5 cm mass, initially diagnosed as a fibroadenoma. The final histopathology after surgical excision revealed a borderline phyllodes tumor with features overlapping those of a fibroadenoma. The second case involved a 59-year-old postmenopausal woman with a rapidly growing mass, which reached 11.9 × 11.3 cm and was initially diagnosed as a fibroadenoma but later confirmed as a borderline malignant phyllodes tumor with focal malignant components. Both cases highlight the limitations of imaging and core biopsy in accurately diagnosing phyllodes tumors and emphasize the need for comprehensive histopathological evaluation. The described clinical cases corresponded to the characteristics of phyllodes tumors indicated in the literature: they appeared in women older than 35 years, were hard to distinguish from fibroadenomas, and required surgical treatment.

Conclusions: Phyllodes tumors are challenging to distinguish from fibroadenomas based on imaging and the initial biopsy results alone. Accurate diagnosis requires thorough histopathological examination following surgical excision. A multidisciplinary approach is essential for optimal management. Our cases show the complexity of phyllodes tumor diagnosis and the importance of considering phyllodes tumors in the differential diagnosis of breast masses, especially when clinical and imaging findings suggest a more aggressive pathology.

从纤维腺瘤到叶状瘤:交界性和巨大性乳腺肿瘤病例分析并文献复习。
背景:叶状瘤是一种非常罕见的乳腺纤维上皮肿瘤,占乳腺肿瘤的不到1%。由于叶状瘤和纤维腺瘤的特征重叠,使用超声或乳房x光检查等成像技术以及组织学方法进行鉴别诊断可能具有挑战性。叶状瘤分为良性、交界性和恶性三种类型,每种类型的复发和转移风险不同。尽管成像和活检技术取得了许多进步,但叶状瘤的诊断仍然具有挑战性。本研究的目的是回顾已有的关于这一主题的文献,并描述两例误诊的叶状瘤。材料和方法:使用Medline (PubMed)数据库进行近10年的文献回顾。有关患者的信息来自乌斯特医院的数据库。通过分析乌斯特医院数据库中2020 - 2023年女性乳房肿块病例,确定了两例误诊的叶状肿瘤。对这2例病例进行回顾性分析。结果:对两例病例的回顾性研究证实了叶状瘤是一种罕见的现象。一位51岁的绝经前妇女出现一个8 × 4 × 5 cm的肿块,最初诊断为纤维腺瘤。手术切除后的最终组织病理学显示为交界性叶状瘤,其特征与纤维腺瘤的特征重叠。第二例患者为59岁绝经后妇女,肿块快速生长,大小为11.9 × 11.3 cm,最初诊断为纤维腺瘤,后证实为交界性叶状恶性肿瘤伴局灶性恶性成分。这两个病例都强调了影像学和核心活检在准确诊断叶状肿瘤方面的局限性,并强调了全面的组织病理学评估的必要性。所描述的临床病例符合文献中指出的叶状瘤的特征:出现于35岁以上的女性,难以与纤维腺瘤区分,需要手术治疗。结论:仅根据影像学和最初的活检结果,叶状瘤很难与纤维腺瘤区分开来。准确的诊断需要在手术切除后进行彻底的组织病理学检查。多学科方法对最佳管理至关重要。我们的病例显示了叶状肿瘤诊断的复杂性,以及考虑叶状肿瘤在乳腺肿块鉴别诊断中的重要性,特别是当临床和影像学结果显示更具侵袭性的病理时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Medica Lituanica
Acta Medica Lituanica Medicine-General Medicine
CiteScore
0.70
自引率
0.00%
发文量
33
审稿时长
16 weeks
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