医学
十二指肠
马尔特淋巴瘤
内镜逆行胰胆管造影术
粘膜相关淋巴组织
淋巴瘤
淋巴系统
病理
放射科
胃肠病学
胰腺炎
作者
Vijaykumar G. Patel,Osama Eltayeb,Vernon J. Henderson,Ralph Lyons,David Martin,Amir Hamami,James K. Fortson,William L. Weaver
出处
期刊:American Surgeon
[SAGE Publishing]
日期:2004-07-01
卷期号:70 (7): 613-616
被引量:10
标识
DOI:10.1177/000313480407000710
摘要
Low-grade lymphoma arising in mucosa-associated lymphoid tissue (MALT) of the duodenum represents a very rare neoplasm. We report an unusual presentation of primary duodenal MALT lymphoma in a 78-year-old man. The patient initially presented with a suspected pulmonary embolus and was anticoagulated, which precipitated a major gastrointestinal hemorrhage. A large atypical ulcer with narrowing of the duodenum beyond the bulb was seen on endoscopy. Biopsies revealed atypical lymphoid cells. Abdominal CT scan revealed a mass in either the duodenum or head of the pancreas. An endoscopic retrograde cholangiopancreatography (ERCP) was performed, which revealed a normal pancreatic duct with a large calculus in the common bile duct, which was extracted after sphincterotomy. Elective surgery was planned for suspected lymphoma of the duodenum. The patient developed severe nausea, vomiting, and fullness after meals. The patient underwent pancreaticoduodectomy for a neoplastic mass causing duodenal obstruction. Pathological examination of the resected specimen revealed a low-grade B-cell lymphoma (MALToma) arising in the duodenum and invading the pancreas. Flow cytometry confirmed the phenotype typical of MALT lymphoma. Celiac, peripancreatic, pelvic, and cervical nodes were also involved with tumor. Bone marrow was also positive for metastasis. The patient was postoperatively treated with chemotherapy for stage IV disease.
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