脾多形性套细胞淋巴瘤和食管腺癌同时发生与BCL1蛋白过表达。

IF 0.6 Q4 ONCOLOGY
Case Reports in Oncological Medicine Pub Date : 2020-12-21 eCollection Date: 2020-01-01 DOI:10.1155/2020/8888829
Dominik Dabrowski, Roberto F Silva, Michael Constantinescu, Rodney E Shackelford, Nestor Dela Cruz, Eric X Wei
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引用次数: 1

摘要

套细胞淋巴瘤(MCL)或中间淋巴细胞淋巴瘤和其他恶性肿瘤的同时发生是罕见的。这些病例提出了诊断和治疗方面的挑战,使他们特别感兴趣的研究。我们报告一例同时性MCL和食道肿瘤在一个老年男性病人。形态学上,肿瘤分为脾多形性MCL和食管腺癌合并发生。多形性MCL模拟弥漫性大B细胞淋巴瘤(DLBCL),但缺乏较大的成中心细胞或免疫母细胞样细胞。奇怪的是,通过免疫组化,两种肿瘤都过表达cyclin D1。这是一个重要的特征,从病理学上区分MCL与两种最接近的鉴别诊断实体:慢性淋巴细胞白血病和DLBCL,后者的套细胞不能转化。淋巴增生FISH显示IGH/CCND1易位,而食管腺癌仅显示CCND1非整倍体,无分离信号。由于胃肠道是MCL累及结外的常见部位,而淋巴瘤性息肉病可表现为胃肠道息肉,因此需要充分注意区分食管腺癌与晚期MCL以及转移性腺癌。尽管研究了大量的免疫组织化学染色,但只有BCL1在两种肿瘤中被证明有部分重叠。患者行食管切除术和脾切除术。随后被诊断为转移性原发性肺鳞状细胞癌,之后患者死亡。MCL通常出现在晚期,被认为是无法治愈的,预后只有几年。目前尚不清楚患者是否死于MCL并发症或转移性鳞状细胞癌。此外,他失去了一年的随访,直到他的第三次癌症被诊断出来后才接受治疗。我们回顾了文献中关于同时性套细胞淋巴瘤和其他实体肿瘤或血液系统恶性肿瘤的先前报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synchronous Occurrence of Splenic Pleomorphic Mantle Cell Lymphoma and Esophageal Adenocarcinoma with Overexpression of BCL1 Protein.

Synchronous Occurrence of Splenic Pleomorphic Mantle Cell Lymphoma and Esophageal Adenocarcinoma with Overexpression of BCL1 Protein.

Synchronous Occurrence of Splenic Pleomorphic Mantle Cell Lymphoma and Esophageal Adenocarcinoma with Overexpression of BCL1 Protein.

Synchronous Occurrence of Splenic Pleomorphic Mantle Cell Lymphoma and Esophageal Adenocarcinoma with Overexpression of BCL1 Protein.

Synchronous occurrences of mantle cell lymphoma (MCL), or intermediate lymphocytic lymphoma, and other malignancies are rare. Such cases present diagnostic and especially therapeutic challenges, making them of particular interest to study. We report a case of synchronic MCL and an esophageal tumor in an elderly male patient. Morphologically, the tumors were classified as splenic pleomorphic MCL and adenocarcinoma of the esophagus occurring concurrently. The pleomorphic MCL mimicked diffuse large B cell lymphoma (DLBCL) but lacked larger centroblast- or immunoblast-like cells. Curiously, both tumors overexpressed cyclin D1 by immunohistochemistry. This is an important feature that distinguishes MCL pathologically from two of its closest entities in the differential diagnosis: chronic lymphocytic leukemia and DLBCL, the latter of which mantle cells cannot transform into. The lymphoproliferation revealed IGH/CCND1 translocation by FISH, but the esophageal adenocarcinoma only showed CCND1 aneuploidy without break-apart signals. Since the gastrointestinal (GI) tract is a common site of extranodal involvement by MCL and lymphomatous polyposis can present as GI polyps, adequate care was taken to differentiate the esophageal adenocarcinoma from advanced stagings of MCL, as well as metastatic adenocarcinoma. Despite numerous immunohistochemical stainings studied, only BCL1 was demonstrated to have partial overlap in both tumors. The patient underwent esophagectomy and splenectomy. A subsequent metastatic primary lung squamous cell carcinoma was diagnosed, after which the patient expired. MCL typically presents at an advanced stage and has been deemed incurable with a prognosis of only several years. It is unclear whether the patient succumbed to complications of his MCL or the metastatic squamous cell carcinoma. Furthermore, he was lost to follow-up for a year and only received treatment after his third cancer was diagnosed. We have reviewed previous reports of synchronic mantle cell lymphoma and other solid tumors or hematological malignancies in the literature.

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来源期刊
自引率
0.00%
发文量
11
审稿时长
16 weeks
期刊介绍: Case Reports in Oncological Medicine is a peer-reviewed, Open Access journal that publishes case reports and case series related to breast cancer, lung cancer, gastrointestinal cancer, skin cancer, head and neck cancer, paediatric oncology, neurooncology as well as genitourinary cancer.
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