一例模仿上皮下肿瘤的食管 MALT 淋巴瘤病例

IF 0.6 Q4 GASTROENTEROLOGY & HEPATOLOGY The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi Pub Date : 2024-04-25 DOI:10.4166/kjg.2024.021
Ha Eun Lee, Gwang Ha Kim, Min Ji Kim, Kyung Bin Kim, Dong Chan Joo, Hye Kyung Jeon, M. Lee, B. Lee
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引用次数: 0

摘要

粘膜相关淋巴组织(MALT)淋巴瘤又称结外边缘区淋巴瘤,是一种低级别B细胞淋巴瘤,可发生在各种器官的粘膜层,包括胃肠道、唾液腺、肺和皮肤。最常见的部位是胃肠道,尤其是胃。另一方面,原发性食管淋巴瘤则极为罕见。MALT 淋巴瘤可在组织学上转化为更具侵袭性的 B 细胞淋巴瘤,如弥漫大 B 细胞淋巴瘤,导致预后不良。本文报告了一例罕见的原发性食管 MALT 淋巴瘤,该淋巴瘤模仿位于食管下段的上皮下肿瘤,通过放疗成功治愈。当发现食管上皮下肿瘤时,尤其是当内镜超声检查发现肿瘤位于粘膜深层和粘膜下层时,应将 MALT 淋巴瘤列入鉴别诊断。精确诊断后,准确的分期和适当的治疗至关重要。有必要进行定期随访,以评估复发或转化为高级别淋巴瘤的可能性。
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A Case of Esophageal MALT Lymphoma Mimicking a Subepithelial Tumor.
Mucosa-associated lymphoid tissue (MALT) lymphoma, also known as extranodal marginal zone lymphoma, is a low-grade B-cell lymphoma that can develop in the mucosal layer of various organs, including the gastrointestinal tract, salivary glands, lungs, and skin. The most common site is the gastrointestinal tract, particularly the stomach. On the other hand, primary esophageal lymphomas are extremely rare. MALT lymphomas can undergo histological transformation into more aggressive B-cell lymphomas, such as diffuse large B-cell lymphoma, resulting in a poor prognosis. This paper reports a rare case of primary esophageal MALT lymphoma mimicking a subepithelial tumor located in the lower esophagus that was treated successfully with radiotherapy. MALT lymphoma should be included in a differential diagnosis when subepithelial tumors are found in the esophagus, particularly if endoscopic ultrasonography reveals the tumor to be located in the deep mucosal and submucosal layers. Following the precise diagnosis, accurate staging and appropriate treatment are crucial. Regular follow-up is necessary to assess the possibility of recurrence or transformation to high-grade lymphoma.
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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
83
审稿时长
24 weeks
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