International journal of hematology · 2021
A case of lymphomatoid granulomatosis with central nervous system involvement successfully treated with IFNα.
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Yamasaki Yoshitaka, Morishige Satoshi, Komaki Satoru, Furuta Takuya, Koga Hiroshi, Oya Shuki, Nakamura Takayuki, Yamaguchi Maki, Aoyama Kazutoshi, Mouri Fumihiko, Osaki Koichi, Nakama Takekuni, Ohshima Koichi, Morioka Motohiro, Nagafuji Koji
Аннотация
Lymphomatoid granulomatosis (LYG) is a rare Epstein-Barr virus (EBV)-driven B-cell lymphoproliferative disease affecting mainly extranodal sites such as the lung, central nervous system (CNS), skin, kidney, and liver. We report a case of low-grade LYG involving the CNS that was successfully treated with interferon alpha (IFNα). A 69-year-old woman developed necrotic erythema of the skin and was initially diagnosed with pyoderma gangrenosum based on skin biopsy. She showed a limited response to prednisolone. Approximately 6 months after the initial onset, low-grade LYG was diagnosed after detection of CNS lesions on brain biopsy. The whole blood EBV-DNA load determined by real-time polymerase chain reaction was slightly elevated. Two months into IFNα therapy, skin and CNS lesions had responded favorably and the EBV-DNA load decreased. IFNα plays an important role in treatment of LYG through its antiproliferative, immunomodulatory, and anti-EBV effects. To our knowledge, this is the first case report of successful treatment with IFNα in Japan. Further investigation is necessary to determine optimal use of IFNα for LYG.