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首页> 外文期刊>American Journal of Surgical Pathology >Gall bladder and extrahepatic bile duct lymphomas: clinicopathological observations and biological implications.
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Gall bladder and extrahepatic bile duct lymphomas: clinicopathological observations and biological implications.

机译:胆囊和肝外胆管淋巴瘤:临床病理观察和生物学意义。

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Lymphomas of the gall bladder and extrahepatic bile ducts are exceedingly rare. We present the clinicopathological features of 19 cases from our files; 14 patients had primary lymphoma (13 involving gall bladder and 1 involving common hepatic duct), while 5 had systemic lymphoma on further work-up. Most patients presented with symptoms mimicking cholecystitis. The most common primary lymphoma types were diffuse large B-cell lymphoma, extranodal marginal zone lymphoma, B-lymphoblastic lymphoma, and follicular lymphoma. Two cases had features of lymphomatous polyposis, one a case of follicular lymphoma and the second a case of mantle cell lymphoma, with disease limited to the mantle zones, so-called in situ mantle cell lymphoma. Other rare lymphoma subtypes not described earlier in this site included the extracavitary variant of primary effusion lymphoma and plasmablastic lymphoma. Patients with diffuse large B-cell lymphoma and extranodal marginal zone lymphoma were older (mean age 75.8 y) than those with other subtypes (mean age 47 y) and more likely to have gallstones (60% vs. 12.5%). A comprehensive literature review revealed 36 primary gall bladder and 16 primary extrahepatic bile duct lymphomas. When compared with primary gall bladder lymphomas, those involving the extrahepatic bile ducts present at a younger age (47 y vs. 63 y) usually with obstructive jaundice, and are less often associated with gallstones (17% vs. 50%) or regional lymph node involvement (6% vs. 31%). In conclusion, primary lymphomas of the gall bladder and extrahepatic bile ducts show a broad spectrum of disease types, but in many respects mirror the spectrum of primary lymphomas of the gastrointestinal tract.
机译:胆囊和肝外胆管淋巴瘤极为罕见。我们从档案中介绍了19例病例的临床病理特征; 14例原发性淋巴瘤(13例涉及胆囊癌,1例涉及肝总管),而5例在进一步检查中患有全身性淋巴瘤。大多数患者表现出模仿胆囊炎的症状。最常见的原发性淋巴瘤类型为弥漫性大B细胞淋巴瘤,结外边缘区淋巴瘤,B淋巴母细胞淋巴瘤和滤泡性淋巴瘤。 2例具有淋巴瘤性息肉病特征,1例为滤泡性淋巴瘤,2例为套细胞淋巴瘤,其疾病仅限于套层区域,即所谓的原位套细胞淋巴瘤。该部位较早时未描述的其他罕见淋巴瘤亚型包括原发渗出性淋巴瘤和浆母细胞性淋巴瘤的腔外变异。弥漫性大B细胞淋巴瘤和结外边缘区淋巴瘤的患者年龄更大(平均年龄75.8岁),比其他亚型(平均年龄47岁)的患者更容易发生胆结石(60%比12.5%)。全面的文献综述显示36例原发性胆囊癌和16例原发性肝外胆管淋巴瘤。与原发性胆囊淋巴瘤相比,累及肝外胆管的患者年龄较小(47岁比63岁),通常伴有梗阻性黄疸,较少与胆结石(17%比50%)或局部淋巴瘤相关节点参与度(6%vs. 31%)。总之,胆囊和肝外胆管的原发性淋巴瘤表现出广泛的疾病类型,但在许多方面反映出胃肠道原发性淋巴瘤的谱。

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