Classical Hodgkin lymphoma type post-transplant lymphoproliferative disorder in a kidney transplant recipient: a diagnostic pitfall

被引:0
作者
Taro Mohri
Yoshihiro Ikura
Asako Hirakoso
Masashi Okamoto
Masakatsu Hishizawa
Akifumi Takaori-Kondo
Seiichi Kato
Shigeo Nakamura
Kai Yoshimura
Hidetoshi Okabe
Yasuhiro Iwai
机构
[1] Takatsuki General Hospital,Department of Pathology
[2] Kobe University Graduate School of Medicine,Department of Pathology
[3] Takatsuki General Hospital,Department of Hematology
[4] Kyoto University Hospital,Department of Hematology
[5] Nagoya University Graduate School of Medicine,Department of Pathology and Laboratory Medicine
[6] Aichi Cancer Center Hospital,Department of Pathology and Molecular Diagnostics
来源
International Journal of Hematology | 2018年 / 108卷
关键词
Classical Hodgkin lymphoma; Post-transplant lymphoproliferative disorder; Immunohistochemistry;
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摘要
We report a case of classical Hodgkin lymphoma type post-transplant lymphoproliferative disorder (HL-PTLD) after kidney transplantation to highlight the difficulty of distinguishing this disorder from Hodgkin lymphoma-like PTLD (HL-like PTLD). Through this case report and literature review, we seek to clarify definitive pathologic features to differentiate these two conditions. A 38-year-old male kidney transplant recipient who had been receiving immunosuppressants was admitted to our hospital with unidentified high fever. Computed tomography images and blood tests indicated a lymphoproliferative disorder. Abdominal lymph node biopsy was performed, and microscopic examination revealed the presence of many large atypical cells in a background of dense T cell accumulation. The large, atypical cells were positive for Epstein–Barr Virus (EBV)-encoded small RNAs (EBER) in situ hybridization, EBV-LMP1, CD30 and PAX5, but negative for CD15, CD20 and CD45. Except for CD15-negativity, this immunohistochemical pattern was consistent with that of classical Hodgkin lymphoma. By close examination of the above immunoreactivities and the patient’s subsequent chemosensitive clinical course, we finally made a diagnosis of HL-PTLD.
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页码:218 / 227
页数:9
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