A case of acute diffuse large B cell lymphoma in an anti-human T-cell leukaemia virus type 1-positive rheumatoid arthritis patient treated with methotrexate, who died.


Journal

Modern rheumatology case reports
ISSN: 2472-5625
Titre abrégé: Mod Rheumatol Case Rep
Pays: England
ID NLM: 101761026

Informations de publication

Date de publication:
07 2020
Historique:
entrez: 22 10 2020
pubmed: 23 10 2020
medline: 27 8 2021
Statut: ppublish

Résumé

A 70-year-old woman was hospitalised due to jaundice and fever. She was diagnosed with rheumatoid arthritis (RA) at 54 years of age. Treatment with methotrexate (MTX) was successful, and her RA was in remission. Five weeks before the hospitalisation, she was diagnosed with optic neuritis due to a decline in the visual acuity of the right eye. She was treated with methylprednisolone pulse therapy, followed by prednisolone (PSL), before the hospitalisation, which were not effective. Blood tests showed increased C-reactive protein (CRP) levels, liver injury, and thrombocytopenia. Abdominal echo revealed numerous enlarged lymph nodes in the hepatic portal region. Malignant lymphoma was suspected due to high serum levels of soluble interleukin-2 receptor. None of the treatments were effective, and she died on the fifth hospital day. Diffuse large B cell lymphoma was diagnosed during the autopsy, which showed infiltration of CD20-positive atypical lymphocytes in almost all organs. Since she was taking MTX, she was diagnosed with immunosuppressive drug-associated lymphoproliferative disease (LPD). Anti-human T-cell leukaemia virus type 1 (HTLV-1) antibody was detected in her serum after her death; however, adult T cell leukaemia/lymphoma was not observed. LPD develops during the treatment of RA with disease modifying anti-rheumatic drugs; however, a rapid clinical course leading to death is rarely observed. Previous reports suggest that T cell dysregulation observed in HTLV-1 may contribute towards the development of B cell lymphoma. We have discussed the possible roles of HTLV-1 in LPD development in this case.

Identifiants

pubmed: 33087004
doi: 10.1080/24725625.2019.1702493
doi:

Substances chimiques

Biomarkers 0
Immunosuppressive Agents 0
Methotrexate YL5FZ2Y5U1

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

161-167

Auteurs

Naomi Yoshida (N)

Division of Rheumatology, Kurume University Medical Center, Kurume, Japan.

Gen Sugiyama (G)

Division of Gastroenterology, Kurume University Medical Center, Kurume, Japan.

Suzuna Sugi (S)

Division of Rheumatology, Kurume University Medical Center, Kurume, Japan.

Koki Satake (K)

Division of Rheumatology, Kurume University Medical Center, Kurume, Japan.

Daisuke Wakasugi (D)

Division of Rheumatology, Kurume University Medical Center, Kurume, Japan.

Satoshi Yamasaki (S)

Division of Rheumatology, Kurume University Medical Center, Kurume, Japan.

Yutaro Mihara (Y)

Department of Pathology, Kurume University School of Medicine, Kurume, Japan.

Kotaro Matsuda (K)

Department of Pathology, Kurume University School of Medicine, Kurume, Japan.

Hiroaki Ida (H)

Division of Respirology, Neurology, and Rheumatology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.

Koichi Ohshima (K)

Department of Pathology, Kurume University School of Medicine, Kurume, Japan.

Rin Yamaguchi (R)

Division of Pathology, Kurume University Medical Center, Kurume, Japan.

Munetoshi Nakashima (M)

Division of Rheumatology, Kurume University Medical Center, Kurume, Japan.

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Classifications MeSH