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胃黏膜相关淋巴组织淋巴瘤合并胰腺非霍奇金淋巴瘤:一例报告。

Gastric mucosa-associated lymphoid tissue lymphoma associated with pancreatic non-Hodgkin's lymphoma: A case report.

机构信息

Cairo University, Cairo, Egypt.

NHTMRI, Cairo, Egypt.

出版信息

Endosc Ultrasound. 2014 Apr;3(Suppl 1):S6-7.

Abstract

UNLABELLED

Mucosa-associated lymphoid tissue (MALT) lymphomas are extranodal lymphomas that arise from B lymphocytes located in the marginal zone of lymphoid follicles. Although, there is a substantial amount of lymphoid tissue in the gastrointestinal tract, MALT lymphomas usually arise in chronically inflamed sites that are normally devoid of lymphoid tissue. The best example is gastric MALT lymphoma that is almost always associated with Helicobacter pylori. Primary pancreatic lymphoma (PPL) is an extremely rare tumor (1% incidence) and is often confused with pancreatic adenocarcinoma. By suspecting PPL on clinical and imaging grounds, surgery and its associated complications can be avoided, since the mainstay of the treatment is non-surgical strategies including chemotherapy. We represent a case of a 45-year-old male presented with abdominal pain and vomiting. Upper endoscopy showed multiple gastric ulcers, biopsies revealed non-specific inflammatory ulcers. The patient was given 4-weeks course of proton pump inhibitor with no improvement. After few months, he complained of severe abdominal pain relieved by leaning forward and associated with repeated vomiting. Upper endoscopy revealed multiple umbilicated gastric masses, 10-20 mm in diameter. Biopsies were taken, histopathology and immunohistochemistry revealed MALT lymphoma. Endoscopic ultrasonography was done to the patient and it showed a pancreatic head mass, fine-needle aspiration was done, histopathology and immunohistochemistry revealed PPL. The patient received chemotherapy for MALT lymphoma with near total relief of symptoms and disappearance of gastric and pancreatic masses.

CONCLUSION

This is a rare case having MALT lymphoma associated with PPL.

摘要

未注明

黏膜相关淋巴组织(MALT)淋巴瘤是起源于位于淋巴滤泡边缘区的 B 淋巴细胞的结外淋巴瘤。尽管胃肠道中有大量的淋巴组织,但 MALT 淋巴瘤通常发生在慢性炎症部位,这些部位通常没有淋巴组织。最好的例子是胃 MALT 淋巴瘤,它几乎总是与幽门螺杆菌有关。原发性胰腺淋巴瘤(PPL)是一种极其罕见的肿瘤(发病率为 1%),常与胰腺腺癌混淆。通过临床和影像学怀疑 PPL,可以避免手术及其相关并发症,因为治疗的主要方法是非手术策略,包括化疗。我们报告了一例 45 岁男性,因腹痛和呕吐就诊。上内窥镜检查显示多个胃溃疡,活检显示非特异性炎症性溃疡。患者接受了 4 周质子泵抑制剂治疗,但无改善。几个月后,他抱怨严重的腹痛,前倾时缓解,并伴有反复呕吐。上内窥镜检查显示多个脐状胃肿块,直径 10-20 毫米。进行了活检,组织病理学和免疫组织化学显示 MALT 淋巴瘤。对患者进行了内镜超声检查,显示胰头肿块,进行了细针抽吸,组织病理学和免疫组织化学显示 PPL。患者接受了 MALT 淋巴瘤的化疗,症状几乎完全缓解,胃和胰腺肿块消失。

结论

这是一例罕见的 MALT 淋巴瘤合并 PPL 的病例。

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