无淋巴结病变的弥漫性B细胞淋巴瘤伴反应性组织细胞增多症,类似恶性组织细胞增多症:三例尸检报告。

C. Sakai, T. Takagi, M. Oguro, S. Wakatsuki, T. Aoi, Kohshi Maruyama
{"title":"无淋巴结病变的弥漫性B细胞淋巴瘤伴反应性组织细胞增多症,类似恶性组织细胞增多症:三例尸检报告。","authors":"C. Sakai, T. Takagi, M. Oguro, S. Wakatsuki, T. Aoi, Kohshi Maruyama","doi":"10.3960/JSLRT1961.31.27","DOIUrl":null,"url":null,"abstract":"The clinical and autopsy findings of three cases of B cell lymphoma simulating malignant histiocytosis are reported. Case 1 was 60y.o. female, case 2 was 75y.o. male and case 3 was 61y.o. female. The presenting symptoms were pyrexia in three cases, dyspnea in case 1 and jaundice in case 2. There was no peripheral lymphadenopathy in these cases. A hyperplasia of monocytes and hemophagocytic histiocytes was seen in their bone marrow and many abnormal lymphoid cells were seen in the marrow of case 3. The lung biopsy revealed infiltration of abnormal cells in case 1. Case 1 and 2 were diagnosed as malignant histiocytosis and case 3 was diagnosed as malignant lymphoma with reactive histiocytosis. After chemotherapy using adriamycin or THP-adriamycin case 1 and 3 improved, however case 2 did not respond. The overall survivals of three cases were 26 months in case 1, 3.5 months in case 2 and 12 months in case 3.The postmortem examination showed that abnormal cells infiltrated diffusely into many organs such as lungs, liver, spleen and kidneys. Neither lymphadenopathy nor tumor-formation was seen. Infiltrating abnormal cells were positive for pan B cell antibody (L26) but negative for pan T cell antibody, lysozyme and S-100 protein.These cases indicate that a part of B cell lymphoma is accompanied by reactive histiocytosis simulating malignant histiocytosis.","PeriodicalId":237003,"journal":{"name":"Journal of the Japan Society of the Reticuloendothelial System","volume":"75 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"11","resultStr":"{\"title\":\"Diffuse B cell lymphoma without lymphadenopathy accompanied by reactive histiocytosis simulating malignant histiocytosis: A report of three autopsy cases.\",\"authors\":\"C. Sakai, T. Takagi, M. Oguro, S. Wakatsuki, T. Aoi, Kohshi Maruyama\",\"doi\":\"10.3960/JSLRT1961.31.27\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The clinical and autopsy findings of three cases of B cell lymphoma simulating malignant histiocytosis are reported. Case 1 was 60y.o. female, case 2 was 75y.o. male and case 3 was 61y.o. female. The presenting symptoms were pyrexia in three cases, dyspnea in case 1 and jaundice in case 2. There was no peripheral lymphadenopathy in these cases. A hyperplasia of monocytes and hemophagocytic histiocytes was seen in their bone marrow and many abnormal lymphoid cells were seen in the marrow of case 3. The lung biopsy revealed infiltration of abnormal cells in case 1. Case 1 and 2 were diagnosed as malignant histiocytosis and case 3 was diagnosed as malignant lymphoma with reactive histiocytosis. After chemotherapy using adriamycin or THP-adriamycin case 1 and 3 improved, however case 2 did not respond. The overall survivals of three cases were 26 months in case 1, 3.5 months in case 2 and 12 months in case 3.The postmortem examination showed that abnormal cells infiltrated diffusely into many organs such as lungs, liver, spleen and kidneys. Neither lymphadenopathy nor tumor-formation was seen. Infiltrating abnormal cells were positive for pan B cell antibody (L26) but negative for pan T cell antibody, lysozyme and S-100 protein.These cases indicate that a part of B cell lymphoma is accompanied by reactive histiocytosis simulating malignant histiocytosis.\",\"PeriodicalId\":237003,\"journal\":{\"name\":\"Journal of the Japan Society of the Reticuloendothelial System\",\"volume\":\"75 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"11\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the Japan Society of the Reticuloendothelial System\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3960/JSLRT1961.31.27\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Japan Society of the Reticuloendothelial System","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3960/JSLRT1961.31.27","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 11

摘要

本文报告三例B细胞淋巴瘤的临床和尸检结果。病例1是60岁。女,病例2,75岁。男,病例3 61岁。女性。临床表现为发热3例,呼吸困难1例,黄疸2例。这些病例均未见外周淋巴结病变。病例3骨髓单核细胞和噬血细胞组织细胞增生,骨髓淋巴样细胞异常。病例1肺活检示异常细胞浸润。病例1、2诊断为恶性组织细胞增多症,病例3诊断为恶性淋巴瘤伴反应性组织细胞增多症。在使用阿霉素或thp阿霉素化疗后,病例1和病例3有所改善,但病例2没有反应。病例1总生存期26个月,病例2总生存期3.5个月,病例3总生存期12个月。尸检显示异常细胞弥漫性浸润至肺、肝、脾、肾等脏器。未见淋巴结病变或肿瘤形成。浸润异常细胞pan B细胞抗体(L26)阳性,pan T细胞抗体、溶菌酶和S-100蛋白阴性。这些病例表明部分B细胞淋巴瘤伴有反应性组织细胞增多症,类似恶性组织细胞增多症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diffuse B cell lymphoma without lymphadenopathy accompanied by reactive histiocytosis simulating malignant histiocytosis: A report of three autopsy cases.
The clinical and autopsy findings of three cases of B cell lymphoma simulating malignant histiocytosis are reported. Case 1 was 60y.o. female, case 2 was 75y.o. male and case 3 was 61y.o. female. The presenting symptoms were pyrexia in three cases, dyspnea in case 1 and jaundice in case 2. There was no peripheral lymphadenopathy in these cases. A hyperplasia of monocytes and hemophagocytic histiocytes was seen in their bone marrow and many abnormal lymphoid cells were seen in the marrow of case 3. The lung biopsy revealed infiltration of abnormal cells in case 1. Case 1 and 2 were diagnosed as malignant histiocytosis and case 3 was diagnosed as malignant lymphoma with reactive histiocytosis. After chemotherapy using adriamycin or THP-adriamycin case 1 and 3 improved, however case 2 did not respond. The overall survivals of three cases were 26 months in case 1, 3.5 months in case 2 and 12 months in case 3.The postmortem examination showed that abnormal cells infiltrated diffusely into many organs such as lungs, liver, spleen and kidneys. Neither lymphadenopathy nor tumor-formation was seen. Infiltrating abnormal cells were positive for pan B cell antibody (L26) but negative for pan T cell antibody, lysozyme and S-100 protein.These cases indicate that a part of B cell lymphoma is accompanied by reactive histiocytosis simulating malignant histiocytosis.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信