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异质性淋巴瘤:胃黏膜相关淋巴组织淋巴瘤和腮腺滤泡性淋巴瘤。

Discordant lymphoma: MALT lymphoma of the stomach and follicular lymphoma of the parotid gland.

作者信息

Yamamoto Yutsuki, Yamochi-Onizuka Toshiko, Shiozawa Eisuke, Kushima Miki, Nakamaki Tsuyoshi, Tomoyasu Shigeru, Kaneko Kazuhiro, Mitamura Keiji, Hoshino Mitsunori, Ishii Hiroshi, Kusano Mitsuo, Ota Hidekazu

机构信息

Second Department of Pathology, Showa University School of Medicine, Tokyo, Japan.

出版信息

Pathol Int. 2003 Aug;53(8):557-62. doi: 10.1046/j.1440-1827.2003.01506.x.

DOI:10.1046/j.1440-1827.2003.01506.x
PMID:12895236
Abstract

More than one histological type of malignant lymphoma can occur simultaneously in an individual. The entity is classified as either composite or discordant lymphoma. Both types of lymphoma, particularly discordant lymphoma comprised of extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue lymphoma (MALT-L) and follicular lymphoma (FL), are rare. We report a case of discordant lymphoma comprising MALT-L in the stomach and FL in the parotid gland. The patient was a 50-year-old Japanese woman who visited the University Hospital of Showa (Tokyo, Japan) because a barium study showed erosive gastric lesions. A gastro-intestinal endoscopy was performed 2 months after the barium study, which showed irregular erosions throughout the stomach body. A gastric biopsy showed MALT-L, and Helicobacter pylori (H. pylori) infection was confirmed. The patient had noticed a painless and elastic hard tumor mass of about 2 cm in diameter in the area of the left parotid gland 6 months before the barium study. We removed the parotid gland tumor and diagnosed it as FL 6 months after the barium study. We were able to diagnose the MALT-L and FL by morphological, immunohistochemical and molecular analyses of paraffin-embedded sections. This appears to be the first reported case of MALT-L and FL occurring together as a discordant lymphoma.

摘要

一个个体中可同时出现不止一种组织学类型的恶性淋巴瘤。该实体被分类为复合型或不一致型淋巴瘤。这两种类型的淋巴瘤,尤其是由黏膜相关淋巴组织淋巴瘤(MALT-L)和滤泡性淋巴瘤(FL)组成的不一致型淋巴瘤都很罕见。我们报告一例胃MALT-L和腮腺FL组成的不一致型淋巴瘤病例。患者为一名50岁日本女性,因钡餐检查显示胃糜烂性病变就诊于昭和大学医院(日本东京)。钡餐检查2个月后进行了胃肠内镜检查,显示整个胃体有不规则糜烂。胃活检显示为MALT-L,并确认有幽门螺杆菌(H. pylori)感染。该患者在钡餐检查前6个月就注意到左腮腺区域有一个直径约2 cm的无痛性、质地硬且有弹性的肿块。钡餐检查6个月后,我们切除了腮腺肿瘤并诊断为FL。通过对石蜡包埋切片进行形态学、免疫组织化学和分子分析,我们得以诊断出MALT-L和FL。这似乎是首例作为不一致型淋巴瘤同时出现MALT-L和FL的报道病例。

相似文献

1
Discordant lymphoma: MALT lymphoma of the stomach and follicular lymphoma of the parotid gland.异质性淋巴瘤:胃黏膜相关淋巴组织淋巴瘤和腮腺滤泡性淋巴瘤。
Pathol Int. 2003 Aug;53(8):557-62. doi: 10.1046/j.1440-1827.2003.01506.x.
2
[Two cases of discordant lymphomas consisting of MALT lymphoma and follicular lymphoma].两例由黏膜相关淋巴组织淋巴瘤(MALT淋巴瘤)和滤泡性淋巴瘤组成的不一致淋巴瘤病例
Rinsho Ketsueki. 2011 Jul;52(7):540-5.
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Simultaneous phenotypically distinct but clonally identical mucosa-associated lymphoid tissue and follicular lymphoma in a patient with Sjögren's syndrome.干燥综合征患者同时出现表型不同但克隆相同的黏膜相关淋巴组织和滤泡性淋巴瘤。
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Importance of extensive staging in patients with mucosa-associated lymphoid tissue (MALT)-type lymphoma.黏膜相关淋巴组织(MALT)型淋巴瘤患者进行广泛分期的重要性。
Br J Cancer. 2000 Aug;83(4):454-7. doi: 10.1054/bjoc.2000.1308.
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MALT-type lymphoma and Warthin's tumour presenting in the same parotid gland.同一腮腺内出现的黏膜相关淋巴组织型淋巴瘤和沃辛瘤。
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Primary gastric follicular lymphoma with parafollicular monocytoid B-cells and lymphoepithelial lesions, mimicking extranodal marginal zone lymphoma of MALT.原发性胃滤泡性淋巴瘤伴滤泡旁单核样B细胞和淋巴上皮病变,酷似黏膜相关淋巴组织结外边缘区淋巴瘤。
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Early gastric MALT lymphoma.
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Mucosa-associated lymphoid tissue lymphoma presented as diffuse swelling of the parotid gland.黏膜相关淋巴组织淋巴瘤表现为腮腺弥漫性肿大。
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Simultaneous early adenocarcinoma and mucosa-associated lymphoid tissue (MALT) lymphoma of the stomach associated with Helicobacter pylori infection.同时发生的胃早期腺癌与黏膜相关淋巴组织(MALT)淋巴瘤,与幽门螺杆菌感染相关。
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Simultaneous occurrence of gastric adenocarcinoma and low-grade gastric lymphoma of mucosa-associated lymphoid tissue.胃腺癌与黏膜相关淋巴组织低度胃淋巴瘤同时发生。
Chang Gung Med J. 2002 Feb;25(2):115-21.

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Diagn Pathol. 2015 Dec 29;10:215. doi: 10.1186/s13000-015-0450-6.
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Discordant bone marrow involvement in non-Hodgkin lymphoma.非霍奇金淋巴瘤中不一致的骨髓受累情况。
Blood. 2016 Feb 25;127(8):965-70. doi: 10.1182/blood-2015-06-651968. Epub 2015 Dec 17.