Endoscopic ultrasound-guided fine needle biopsy diagnosis of circumferentially extraluminal mucosa-associated lymphoid tissue lymphoma in the transverse colon: a case report.

IF 0.8 Q4 GASTROENTEROLOGY & HEPATOLOGY
Clinical Journal of Gastroenterology Pub Date : 2024-06-01 Epub Date: 2024-04-12 DOI:10.1007/s12328-024-01945-8
Tomoyuki Niwa, Moeka Watahiki, Toshikatsu Kosugi, Daisuke Kusama, Hiroki Tamakoshi, Masaki Takinami, Junichi Kaneko, Yurimi Takahashi, Masafumi Nishino, Takanori Yamada
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Abstract

A 61-year-old man present to us with continued abdominal pain without abdominal tenderness for 1 month. Blood testing showed elevated biliary enzymes and inflammation. Contrast-enhanced computed tomography (CT) revealed thickening of the transverse colon with relatively strong enhancement but no bile duct dilatation. Colonoscopy revealed localized edema and granular mucosa in the transverse colon. Fluoroscopic endoscopy exhibited the absence of haustra. Multiple biopsies were performed, but differentiation between mild inflammation and mucosa-associated lymphoid tissue (MALT) lymphoma was inconclusive. To establish a definitive diagnosis, transgastric endoscopic ultrasound-guided fine needle biopsy of the hypoechoic mass was performed. Histopathological analysis exhibited the proliferation of small-sized lymphocytes. Fluorescence in situ hybridization revealed the characteristic API2-MALT1 translocation of MALT lymphoma. We performed liver biopsy to investigate biliary enzyme elevation. Histopathology confirmed lymphocytic infiltration within Glisson's capsule. Immunohistochemistry showed positive for CD20 and negative for CD3 and CD5, signifying the infiltration of MALT lymphoma in the liver. Based on these findings, we diagnosed MALT lymphoma, Lugano classification Stage IV. We performed bendamustine-rituximab (BR)-combined therapy. After six courses of BR-combined therapy, colonoscopy revealed improvement in the lead pipe sign and CT revealed disappearance of the mass.

内镜超声引导下细针活检诊断出横结肠周向腔外黏膜相关淋巴组织淋巴瘤:病例报告。
一名 61 岁的男子因持续腹痛 1 个月,无腹部压痛而就诊。血液检查显示胆汁酶和炎症升高。对比增强计算机断层扫描(CT)显示横结肠增厚,增强相对较强,但无胆管扩张。结肠镜检查发现横结肠局部水肿,粘膜呈颗粒状。透视内镜检查显示没有胆管。进行了多次活检,但无法确定是轻度炎症还是粘膜相关淋巴组织(MALT)淋巴瘤。为了明确诊断,医生在经胃内窥镜超声引导下对低回声肿块进行了细针活检。组织病理学分析显示,小体积淋巴细胞增生。荧光原位杂交显示了MALT淋巴瘤特有的API2-MALT1易位。我们进行了肝脏活检,以研究胆汁酶升高的情况。组织病理学证实淋巴细胞浸润在格利森氏囊内。免疫组化显示 CD20 阳性,CD3 和 CD5 阴性,表明肝内有 MALT 淋巴瘤浸润。根据这些结果,我们诊断为 MALT 淋巴瘤,卢加诺分类 IV 期。我们进行了苯达莫司汀-利妥昔单抗(BR)联合治疗。经过六个疗程的BR联合治疗后,结肠镜检查显示铅管征有所改善,CT显示肿块消失。
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来源期刊
Clinical Journal of Gastroenterology
Clinical Journal of Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
2.00
自引率
0.00%
发文量
182
期刊介绍: The journal publishes Case Reports and Clinical Reviews on all aspects of the digestive tract, liver, biliary tract, and pancreas. Critical Case Reports that show originality or have educational implications for diagnosis and treatment are especially encouraged for submission. Personal reviews of clinical gastroenterology are also welcomed. The journal aims for quick publication of such critical Case Reports and Clinical Reviews.
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