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2
Diffuse large B-cell lymphoma: 2019 update on diagnosis, risk stratification, and treatment.弥漫性大 B 细胞淋巴瘤:诊断、风险分层和治疗的 2019 年更新。
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乳腺癌与难治性弥漫性大B细胞腹部淋巴瘤的同步发生:治疗及文献综述

Synchronous occurrence of breast cancer and refractory diffuse large B-cell abdominal lymphoma: Management and review of the literature.

作者信息

Salemis Nikolaos S

机构信息

Breast Cancer Surgery Unit, Army General Hospital, Athens, Greece.

IASO Women's Hospital, Athens, Greece.

出版信息

Intractable Rare Dis Res. 2021 May;10(2):131-135. doi: 10.5582/irdr.2021.01017.

DOI:10.5582/irdr.2021.01017
PMID:33996360
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8122319/
Abstract

The synchronous occurrence of primary breast cancer and lymphoid tissue malignant tumors has been rarely reported in the literature. We present an exceedingly rare case of synchronous breast invasive ductal carcinoma with an abdominal diffuse large B-cell lymphoma (DLBCL). A 78-year-old woman who was diagnosed with a luminal A invasive breast cancer on core biopsy, and complaint of progressively worsening low back pain. An abdominal computed tomography (CT) scan that was performed as part of the preoperative staging showed a large abdominal mass measuring 10.5 × 4.8 × 9.5 cm surrounding the lower part of the abdominal aorta, the right common iliac, right external, right internal iliac, and the left internal iliac arteries. A CT-guided fine-needle aspiration biopsy (FNAB) of the abdominal mass was then performed, to exclude the possibility of being an abdominal tumor metastasis of the known primary breast cancer. Histopathological findings were suggestive of DLBCL. Following a multidisciplinary team discussion, chemotherapy was initiated for DLBCL. The tumor however was refractory to multiple chemotherapy regimens and exhibited a highly aggressive clinical course. The diagnostic evaluation and management of the patient are discussed, along with a review of the relevant literature. This case underscores the fact that the presence of synchronous malignancies may pose both diagnostic and treatment challenges. Accurate staging of both malignancies and multidisciplinary team discussion is of utmost importance to guide an optimal therapeutic approach. Histopathological evaluation is essential for both tumors, for the second malignancy not to be misinterpreted as a secondary deposit of the primary one.

摘要

原发性乳腺癌与淋巴组织恶性肿瘤同时发生的情况在文献中鲜有报道。我们报告了一例极其罕见的原发性乳腺浸润性导管癌与腹部弥漫性大B细胞淋巴瘤(DLBCL)同时发生的病例。一名78岁女性,在粗针活检时被诊断为管腔A型浸润性乳腺癌,并主诉下背部疼痛逐渐加重。作为术前分期的一部分进行的腹部计算机断层扫描(CT)显示,在腹主动脉下部、右侧髂总动脉、右侧股动脉、右侧髂内动脉和左侧髂内动脉周围有一个10.5×4.8×9.5 cm的巨大腹部肿块。随后对腹部肿块进行了CT引导下细针穿刺活检(FNAB),以排除已知原发性乳腺癌发生腹部肿瘤转移的可能性。组织病理学检查结果提示为DLBCL。经过多学科团队讨论,开始对DLBCL进行化疗。然而,该肿瘤对多种化疗方案均耐药,临床病程高度侵袭性。本文讨论了该患者的诊断评估和治疗,并对相关文献进行了综述。该病例强调了同时发生的恶性肿瘤可能带来诊断和治疗挑战这一事实。对两种恶性肿瘤进行准确分期和多学科团队讨论对于指导最佳治疗方法至关重要。组织病理学评估对两种肿瘤都至关重要,以免将第二种恶性肿瘤误诊为第一种的继发性转移灶。