| Literature DB >> 22706531 |
Yasuharu Sato1, Koh-Ichi Ohshima, Katsuyoshi Takata, Xingang Huang, Wei Cui, Kyotaro Ohno, Tadashi Yoshino.
Abstract
IgG4-related disease is a recently proposed clinical entity with several unique clinicopathological features. A chronic inflammatory state with marked fibrosis, which can often be mistaken for malignancy, especially by clinical imaging analyses, unifies these features. In the present report, we describe a case of IgG4-producing mucosa-associated lymphoid tissue lymphoma mimicking IgG4-related disease. The patient was a 55-year-old male who was being followed for right orbital tumor over 1.5 years. The lesion had recently increased in size, so a biopsy was performed. Histologically, the lesion was consistent with IgG4-related disease ; however, IgG4<sup>+</sup> plasma cells showed immunoglobulin light-chain restriction and immunoglobulin heavy chain gene rearrangement was detected in the lesion. Therefore, the lesion was diagnosed as IgG4-producing mucosa-associated lymphoid tissue lymphoma. In conclusion, in histological diagnosis of IgG4-related disease, it is important to examine not only IgG4-immunostain but also immunoglobulin light-chain restriction.Entities:
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Year: 2012 PMID: 22706531 DOI: 10.3960/jslrt.52.51
Source DB: PubMed Journal: J Clin Exp Hematop ISSN: 1346-4280