Peripheral T cell lymphoma with a high titer of proteinase-3-antineutrophil cytoplasmic antibodies that resembled Wegener's granulomatosis

Tsuyoshi Shirai, Reiko Takahashi, Yumi Tajima, Katsura Kohata, Joji Yamamoto, Hiroshi Fujii, Naruhiko Takasawa, Kenichi Ishizawa, Ryo Ichinohasama, Tomonori Ishii, Hideo Harigae

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)

Abstract

Here, we present a 54-year-old man with proptosis and swelling below the left eyelid. Laboratory findings showed high levels of PR3-ANCA and histological examination of the first biopsy revealed acute inflammation. Together with the findings of MRI, a diagnosis of WG was made. However, the disease progressed rapidly and histological examination of the second biopsy revealed infiltration of neoplastic T lymphocytes with aberrant loss of CD7. A final diagnosis of peripheral T cell lymphoma, not otherwise specified (WHO) was made, and complete remission was achieved by chemotherapy. This is a very rare case of T cell lymphoma with a high titer of PR3-ANCA.

Original languageEnglish
Pages (from-to)2041-2045
Number of pages5
JournalInternal Medicine
Volume48
Issue number23
DOIs
Publication statusPublished - 2009

All Science Journal Classification (ASJC) codes

  • Internal Medicine

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