Interleukin-6-producing Intravascular Large B-cell Lymphoma with Lymphadenopathy Mimicking the Histology of Multicentric Castleman Disease

An inguinal lymph node biopsy of a woman with a one-month history of a progressive fever, fatigue, dyspnea, skin rash, and lymphadenopathy revealed a well-preserved basic structure, hyperplastic germinal centers, and an interfollicular region containing polyclonal plasma cell sheets, suggesting plas...

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Veröffentlicht in:Internal Medicine 2020/12/01, Vol.59(23), pp.3061-3065
Hauptverfasser: Shiroshita, Kohei, Kikuchi, Taku, Okayama, Mikio, Kasahara, Hidenori, Kamiya, Takahiro, Shimizu, Takayuki, Kurose, Nozomu, Masaki, Yasufumi, Okamoto, Shinichiro
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container_end_page 3065
container_issue 23
container_start_page 3061
container_title Internal Medicine
container_volume 59
creator Shiroshita, Kohei
Kikuchi, Taku
Okayama, Mikio
Kasahara, Hidenori
Kamiya, Takahiro
Shimizu, Takayuki
Kurose, Nozomu
Masaki, Yasufumi
Okamoto, Shinichiro
description An inguinal lymph node biopsy of a woman with a one-month history of a progressive fever, fatigue, dyspnea, skin rash, and lymphadenopathy revealed a well-preserved basic structure, hyperplastic germinal centers, and an interfollicular region containing polyclonal plasma cell sheets, suggesting plasma cell-type multicentric Castleman disease (MCD). We initiated prednisolone and anti-interleukin (IL)-6 antibody (tocilizumab), without success. A biopsy specimen re-evaluation detected CD20-positive atypical large B cells infiltrating the small vessels within and around the lymph node and its capsule. We diagnosed her with intravascular large B-cell lymphoma (IVLBCL). Lymphoma cells were weakly positive for IL-6 by immunohistochemical staining. IL-6 from lymphoma cells may have caused the MCD-like presentation as a paraneoplastic etiology. Malignant lymphoma should be excluded before diagnosing MCD.
doi_str_mv 10.2169/internalmedicine.5046-20
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Med.</addtitle><description>An inguinal lymph node biopsy of a woman with a one-month history of a progressive fever, fatigue, dyspnea, skin rash, and lymphadenopathy revealed a well-preserved basic structure, hyperplastic germinal centers, and an interfollicular region containing polyclonal plasma cell sheets, suggesting plasma cell-type multicentric Castleman disease (MCD). We initiated prednisolone and anti-interleukin (IL)-6 antibody (tocilizumab), without success. A biopsy specimen re-evaluation detected CD20-positive atypical large B cells infiltrating the small vessels within and around the lymph node and its capsule. We diagnosed her with intravascular large B-cell lymphoma (IVLBCL). Lymphoma cells were weakly positive for IL-6 by immunohistochemical staining. IL-6 from lymphoma cells may have caused the MCD-like presentation as a paraneoplastic etiology. 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Med.</addtitle><date>2020-12-01</date><risdate>2020</risdate><volume>59</volume><issue>23</issue><spage>3061</spage><epage>3065</epage><pages>3061-3065</pages><issn>0918-2918</issn><eissn>1349-7235</eissn><abstract>An inguinal lymph node biopsy of a woman with a one-month history of a progressive fever, fatigue, dyspnea, skin rash, and lymphadenopathy revealed a well-preserved basic structure, hyperplastic germinal centers, and an interfollicular region containing polyclonal plasma cell sheets, suggesting plasma cell-type multicentric Castleman disease (MCD). We initiated prednisolone and anti-interleukin (IL)-6 antibody (tocilizumab), without success. A biopsy specimen re-evaluation detected CD20-positive atypical large B cells infiltrating the small vessels within and around the lymph node and its capsule. We diagnosed her with intravascular large B-cell lymphoma (IVLBCL). Lymphoma cells were weakly positive for IL-6 by immunohistochemical staining. IL-6 from lymphoma cells may have caused the MCD-like presentation as a paraneoplastic etiology. Malignant lymphoma should be excluded before diagnosing MCD.</abstract><cop>Japan</cop><pub>The Japanese Society of Internal Medicine</pub><pmid>32759587</pmid><doi>10.2169/internalmedicine.5046-20</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
B-cell lymphoma
B-Lymphocytes - pathology
Biopsy
Case Report
Castleman Disease - diagnosis
Castleman Disease - pathology
Castleman's disease
CD20 antigen
Cytokines
Diagnosis, Differential
Dyspnea
Etiology
Female
Fever
Germinal centers
Humans
Interleukin 6
Interleukin-6 - biosynthesis
Internal medicine
intravascular large B-cell lymphoma
Lymph nodes
Lymph Nodes - pathology
Lymphadenopathy
Lymphadenopathy - complications
Lymphadenopathy - pathology
Lymphatic system
Lymphocytes B
Lymphoma, Large B-Cell, Diffuse - complications
Lymphoma, Large B-Cell, Diffuse - pathology
Mimicry
multicentric Castleman disease
paraneoplastic syndrome
Prednisolone
Respiration
title Interleukin-6-producing Intravascular Large B-cell Lymphoma with Lymphadenopathy Mimicking the Histology of Multicentric Castleman Disease
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