Primary breast lymphoma mimicking triple-negative breast cancer: a case report with clinical and pathological implications.

IF 0.7 Q4 SURGERY
Toyoaki Sawano, Masahiro Wada, Akihiko Ozaki, Akinori Hashiguchi, Shinichi Hirooka, Tetsuya Tanimoto
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Abstract

Background: Primary breast lymphoma (PBL) is a rare type of extranodal lymphoma, the diagnostic process for which presents significant challenges owing to an overlap in clinical and pathological features with those observed in triple-negative breast cancer (TNBC). However, the current literature reveals a paucity of information regarding the ramifications of potential diagnostic errors, particularly in the context of emergent therapeutic strategies for TNBC. Thus, we present a unique report of a case of PBL.

Case presentation: A 76-year-old female with no past medical or family history presented to the hospital with the chief complaint of a mass in the right breast. Two masses were palpated in the right breast: one 56 mm mass (No. 1) located at 10 o'clock, and a 21 mm large, elastic, hard mass (No. 2) at 4 o'clock. Needle biopsy was performed only on the larger 56 mm mass (No. 1). The results showed invasive carcinoma that was negative for estrogen receptor, progesterone receptor, and human epidermal growth factor receptor-2. The preoperative diagnosis was right breast cancer (T3N0M0 Stage IIB) of the TNBC subtype. The patient refused the preoperative chemotherapy recommended by the treatment team; therefore, right breast mastectomy and sentinel lymph-node biopsy were performed instead. The histopathological diagnosis of the first mass was diffuse large B-cell lymphoma (DLBCL); that of the second mass (No. 2) was an invasive breast carcinoma of no special type. Postoperative treatment consisted of endocrine therapy (letrozole) for breast cancer, while the DLBCL was treated with chemotherapy and three courses of intrathecal chemotherapy. At the time of this report, the patient is still living, and neither tumor had recurred in the 2 years following surgery.

Conclusions: On rare occasions, PBL can preoperatively mimic TNBC. While this case did not lead to serious consequences, because surgery was eventually selected as the first therapy, clinicians should be aware that the diagnosis of PBL is challenging using only a core-needle biopsy and can often be misdiagnosed as TNBC.

模仿三阴性乳腺癌的原发性乳腺淋巴瘤:一份具有临床和病理意义的病例报告。
背景:原发性乳腺淋巴瘤(PBL)是一种罕见的结外淋巴瘤:原发性乳腺淋巴瘤(PBL)是一种罕见的结节外淋巴瘤,由于其临床和病理特征与三阴性乳腺癌(TNBC)的临床和病理特征存在重叠,因此诊断过程面临巨大挑战。然而,现有文献显示,有关潜在诊断错误的后果的信息很少,尤其是在 TNBC 的新兴治疗策略背景下。因此,我们报告了一例独特的 PBL 病例:一名 76 岁的女性,既往无病史也无家族史,以右侧乳房肿块为主诉到医院就诊。在右侧乳房摸到两个肿块:一个是位于 10 点钟位置的 56 毫米肿块(1 号),另一个是位于 4 点钟位置的 21 毫米大、有弹性、硬的肿块(2 号)。只对较大的 56 毫米肿块(1 号)进行了针刺活检。结果显示为浸润性癌,雌激素受体、孕酮受体和人类表皮生长因子受体-2均为阴性。术前诊断为 TNBC 亚型右乳腺癌(T3N0M0 IIB 期)。患者拒绝接受治疗小组建议的术前化疗,因此改行右乳切除术和前哨淋巴结活检。第一个肿块的组织病理学诊断为弥漫大 B 细胞淋巴瘤(DLBCL);第二个肿块(2 号)的组织病理学诊断为无特殊类型的浸润性乳腺癌。术后治疗包括乳腺癌内分泌治疗(来曲唑),而 DLBCL 则接受了化疗和三个疗程的鞘内化疗。在撰写本报告时,患者仍在世,术后两年内肿瘤均未复发:结论:在极少数情况下,PBL可在术前模拟TNBC。虽然本病例最终选择了手术作为第一治疗方法,没有导致严重后果,但临床医生应该意识到,仅使用核心针活检诊断PBL具有挑战性,而且经常会被误诊为TNBC。
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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审稿时长
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