| Literature DB >> 23666666 |
Takeki Mitsui1, Akihiko Yokohama, Hiromi Koiso, Takuma Ishizaki, Hideki Uchiumi, Takayuki Saitoh, Hiroshi Handa, Junko Hirato, Masamitsu Karasawa, Hirokazu Murakami, Masaru Kojima, Yoshihisa Nojima, Norifumi Tsukamoto.
Abstract
Reported is a rare case IgG4-related disease that developed 10 years after combination chemotherapy for non-Hodgkin lymphoma. A 59-year-old Japanese man with longstanding bronchial asthma was referred to our hospital for bilateral hilar lymph node enlargement. The initial diagnosis was diffuse large B cell lymphoma (DLBCL) by supraclavicular lymph node biopsy. Serum IgG was high (4550 mg/dL) at diagnosis. The patient achieved complete response following six cycles of combination chemotherapy. Ten years later, bilateral submaxillary gland swelling was observed. Serum IgG and IgG4 were 2909 and 1470 mg/dL, respectively. The patient was diagnosed with IgG4-related disease by submandibular lymph node biopsy. Due to the difficulty in distinguishing IgG4-related disease from DLBCL through imaging findings alone, pathological confirmation of such lesions by biopsy is mandatory before proceeding to treatment.Entities:
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Year: 2013 PMID: 23666666 DOI: 10.1007/s12185-013-1359-z
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490