[Delayed diagnosis of hydroa vacciniforme-like lymphoproliferative disorder in a patient with skin rashes].

Chronic active Epstein-Barr virus infection EBV-associated T- or NK-cell lymphoproliferative diseases Facial skin eruption Hydroa vacciniforme lymphoproliferative disorder

Journal

[Rinsho ketsueki] The Japanese journal of clinical hematology
ISSN: 0485-1439
Titre abrégé: Rinsho Ketsueki
Pays: Japan
ID NLM: 2984782R

Informations de publication

Date de publication:
2023
Historique:
medline: 7 4 2023
entrez: 5 4 2023
pubmed: 6 4 2023
Statut: ppublish

Résumé

Chronic active Epstein-Barr virus (CAEBV) infection is characterized by persistent EBV infection and can lead to fatal conditions such as hemophagocytic syndrome and malignant lymphoma through the clonal expansion of EBV-infected T or natural killer (NK) cells. Hydroa vacciniforme lymphoproliferative disorder (HV) and hypersensitivity to mosquito bites (HMB) have been identified as skin diseases in EBV-associated T- or NK-cell lymphoproliferative diseases. We present the case of a 33-year-old man. The patient had frequent episodes of a facial rash for three years before he visited our hospital, he visited several dermatologists but did not receive a diagnosis of HV. He was referred to the hematology department of our hospital for assessment of atypical lymphocytes in peripheral blood. Based on routine blood and bone marrow test we were unable to diagnose HV. However, when the patient's liver function deteriorated six months later, we considered the possibility of HV after reevaluating the skin rash. After performing EBV-related tests, we were able to definitively diagnose CAEBV with HV. It is crucial to be able to connect clinical observations to EBV-related tests when diagnosing CAEBV. Hematologists must be knowledgeable of the EBV-associated skin conditions of HV and HMB.

Identifiants

pubmed: 37019675
doi: 10.11406/rinketsu.64.209
doi:

Types de publication

Case Reports English Abstract Journal Article

Langues

jpn

Sous-ensembles de citation

IM

Pagination

209-213

Auteurs

Yuka Umeki (Y)

Department of Hematology, Hyogo Prefectural Nishinomiya Hospital.

Mako Ikeda (M)

Department of Hematology, Hyogo Prefectural Nishinomiya Hospital.

Wataru Nakahara (W)

Department of Hematology, Hyogo Prefectural Nishinomiya Hospital.

Mizuki Asako (M)

Department of Hematology, Hyogo Prefectural Nishinomiya Hospital.

Yoshiki Matsuoka (Y)

Department of Hematology, Hyogo Prefectural Nishinomiya Hospital.

Takuya Terakawa (T)

Department of Hematology, Hyogo Prefectural Nishinomiya Hospital.

Hitomi Matsunaga (H)

Department of Hematology, Hyogo Prefectural Nishinomiya Hospital.

Rei Tadokoro (R)

Department of Rheumatology, Hyogo Prefectural Nishinomiya Hospital.

Masahiro Sekiguchi (M)

Department of Rheumatology, Hyogo Prefectural Nishinomiya Hospital.

Takahiro Matsui (T)

Department of Pathology, Osaka University Graduate School of Medicine.

Kazumasa Oka (K)

Department of Pathology, Hyogo Prefectural Nishinomiya Hospital.

Kohei Higuchi (K)

Department of Hematology/Oncology, Osaka Medical Center and Research Institute for Maternal and Child Health.

Akihisa Sawada (A)

Department of Hematology/Oncology, Osaka Medical Center and Research Institute for Maternal and Child Health.

Masami Inoue (M)

Department of Hematology/Oncology, Osaka Medical Center and Research Institute for Maternal and Child Health.

Shuji Ueda (S)

Department of Hematology, Hyogo Prefectural Nishinomiya Hospital.

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