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双子宫宫颈恶性淋巴瘤,考虑为肾移植术后患者的移植后淋巴细胞增生性疾病:一例报告。

Malignant lymphoma of the cervix in a bicollis uterus considered to be a post-transplant lymphoproliferative disorder in a patient after renal transplantation: A case report.

作者信息

Yoshida Yu, Izumi Ririko, Iwashita Saki, Nakashima Natsumi, Kishida Kaori, Imachi Yuzo, Shimada Yukiyo, Maehara Kana, Wada Tomoko, Ando Mariko, Hamasaki Yoichiro, Kurihara Shuichi, Onjo Sachiko, Nishida Makoto

机构信息

Department of Obstetrics and Gynecology, Japanese Red Cross Fukuoka Hospital, 3-1-1 Ohgusu, Minami-ku, Fukuoka 815-8555, Japan.

出版信息

Gynecol Oncol Rep. 2020 Nov 21;34:100676. doi: 10.1016/j.gore.2020.100676. eCollection 2020 Nov.

DOI:10.1016/j.gore.2020.100676
PMID:33304978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7718170/
Abstract

Post-transplant lymphoproliferative disorder (PTLD) refers to a group of diseases, characterized by abnormal proliferation of lymphocytes, that develop after organ transplantation. PTLD is associated with poor prognosis, and has become a major problem for transplant patients. In this report, we described a case of malignant lymphoma of the cervix in a bicollis uterus considered to be a PTLD in a patient after renal transplantation. The incidence of this disease is expected to increase as the survival rate of transplant patients improves. Hence, it is very important for gynecological oncologists to consider the presence of PTLD when examining such patients.

摘要

移植后淋巴细胞增生性疾病(PTLD)是指一组在器官移植后发生的、以淋巴细胞异常增殖为特征的疾病。PTLD预后较差,已成为移植患者面临的一个主要问题。在本报告中,我们描述了一例肾移植术后患者发生在双子宫宫颈的恶性淋巴瘤,该淋巴瘤被认为是PTLD。随着移植患者生存率的提高,预计这种疾病的发病率将会增加。因此,妇科肿瘤学家在检查此类患者时考虑PTLD的存在非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e37/7718170/06ad48c86795/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e37/7718170/90bd9199b4e0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e37/7718170/870db7226214/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e37/7718170/06ad48c86795/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e37/7718170/90bd9199b4e0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e37/7718170/870db7226214/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e37/7718170/06ad48c86795/gr3.jpg

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本文引用的文献

1
Post-transplantation lymphoproliferative disorders: Current concepts and future therapeutic approaches.移植后淋巴细胞增生性疾病:当前概念与未来治疗方法
World J Transplant. 2020 Feb 28;10(2):29-46. doi: 10.5500/wjt.v10.i2.29.
2
Primary lymphoma of the female genital tract: An analysis of 697 cases.女性生殖道原发性淋巴瘤:697例病例分析。
Gynecol Oncol. 2017 May;145(2):305-309. doi: 10.1016/j.ygyno.2017.02.043. Epub 2017 Mar 9.
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Clinical outcomes of abnormal cervical cytology and human papillomavirus-related lesions in patients with organ transplantation: 11-year experience at a single institution.
器官移植患者异常宫颈细胞学和人乳头瘤病毒相关病变的临床转归:单中心 11 年经验。
Int J Clin Oncol. 2016 Aug;21(4):730-734. doi: 10.1007/s10147-015-0940-2. Epub 2015 Dec 22.
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Risk factors for Epstein-Barr virus-related post-transplant lymphoproliferative disease after allogeneic hematopoietic stem cell transplantation.异基因造血干细胞移植后与 EBV 相关的移植后淋巴增殖性疾病的危险因素。
Haematologica. 2014 Feb;99(2):346-52. doi: 10.3324/haematol.2013.087338. Epub 2013 Sep 20.
5
Post-transplant lymphoproliferative disorder involving the ovary as an initial manifestation: a case report.以卵巢为首发表现的移植后淋巴细胞增生性疾病:一例报告
J Med Case Rep. 2010 Jun 18;4:184. doi: 10.1186/1752-1947-4-184.
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Posttransplant lymphoproliferative disorders in kidney transplant recipients: an Iranian multicenter experience.肾移植受者的移植后淋巴增殖性疾病:一项伊朗多中心研究经验。
Iran J Kidney Dis. 2008 Oct;2(4):227-33.
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Post-transplant lymphoproliferative disorders (PTLD) after solid organ transplantation.实体器官移植后的移植后淋巴细胞增生性疾病(PTLD)
Crit Rev Oncol Hematol. 2005 Oct;56(1):155-67. doi: 10.1016/j.critrevonc.2005.03.015.
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Post-transplant lymphoproliferative disorder of the cervix.
Gynecol Oncol. 2005 Apr;97(1):271-5. doi: 10.1016/j.ygyno.2004.12.049.
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Epstein-Barr virus-negative post-transplant lymphoproliferative disorders: a distinct entity?爱泼斯坦-巴尔病毒阴性的移植后淋巴组织增生性疾病:一种独特的实体?
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Reticulum cell sarcoma after renal homotransplantation and azathioprine and prednisone therapy.肾同种移植及硫唑嘌呤和泼尼松治疗后发生的网状细胞肉瘤
Br Med J. 1968 Dec 21;4(5633):746-8. doi: 10.1136/bmj.4.5633.746.