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伪装成良性肿瘤的原发性食管黏膜相关淋巴组织淋巴瘤。

Primary mucosa-associated lymphoid tissue lymphoma of the esophagus masquerading as a benign tumor.

作者信息

Bardisi Ekhlas S, Alghanmi Najla, Merdad Adnan A

机构信息

Department of Surgery, KAUH, Jeddah, Saudi Arabia.

Department of Pathology, KAUH, Jeddah, Saudi Arabia.

出版信息

Ann Med Surg (Lond). 2014 May 20;3(2):39-42. doi: 10.1016/j.amsu.2014.05.001. eCollection 2014 Jun.

Abstract

We report a case of primary esophageal low-grade B-cell lymphoma of MALT type in a 50-year-old Saudi male patient who presented to our hospital with a history of dysphagia and heartburn for more than 2 years. Endoscopy showed a large esophageal mass with an intact mucosa located in the distal esophagus, 28 cm-35 cm from the incisor teeth. Endoscopic ultrasonography (EUS) showed a large well demarcated sub-epithelial lesion 4 cm in width and 10 cm in length arising from the muscularis mucosa with mixed echogenicity consistent with benign leiomyoma. Subsequently, the patient underwent surgical resection of the tumor; the histopathology confirmed the diagnosis of esophageal lymphoma. The tumor was considered to be completely resected and therefore additional treatment was not administered. The patient was doing well on follow up after treatment. Clinically and radiologically he did not reveal any signs of recurrence. Surgical resection is beneficial as a primary treatment option in incipient primary low grade MALT esophageal lymphomas.

摘要

我们报告一例原发性食管MALT型低度B细胞淋巴瘤,患者为一名50岁的沙特男性,因吞咽困难和烧心病史超过2年前来我院就诊。内镜检查显示食管远端有一个大的食管肿物,黏膜完整,距门齿28厘米至35厘米。内镜超声检查(EUS)显示一个界限清楚的大的上皮下病变,宽4厘米,长10厘米,起源于黏膜肌层,回声混合,符合良性平滑肌瘤。随后,患者接受了肿瘤手术切除;组织病理学确诊为食管淋巴瘤。肿瘤被认为已完全切除,因此未给予额外治疗。治疗后随访期间患者情况良好。临床和影像学检查均未发现复发迹象。对于早期原发性低度MALT型食管淋巴瘤,手术切除作为主要治疗选择是有益的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e24/4268481/ea19d643fb28/gr1.jpg

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