Literature DB >> 21123969

Atypical lymphoplasmacytic and immunoblastic proliferation of autoimmune disease : clinicopathologic and immunohistochemical study of 9 cases.

Masaru Kojima1, Naoya Nakamura, Norihumi Tsukamoto, Hideaki Itoh, Hazuki Matsuda, Satsuki Kobayashi, Kazue Ueki, Hiroyuki Irisawa, Kayoko Murayama, Tadahiko Igarashi, Nobuhide Masawa, Shigeo Nakamura.   

Abstract

Atypical lymphoplasmacytic immunoblastic proliferation (ALPIB) is a rare lymphoproliferative disorder (LPD) associated with autoimmune disease (AID). To further clarify the clinicopathologic, immunohistological, and genotypic findings of ALPIB in lymph nodes associated with well-documented AIDs, 9 cases are presented. These 9 patients consisted of 4 patients with systemic lupus erythematosus, 3 patients with rheumatoid arthritis, and one case each with Sjögren's syndrome and dermatomyositis. All 9 patients were females aged from 25 to 71 years with a median age of 49 years. Four cases presented with lymphadenopathy as the initial manifestation. In 4 patients, immunosuppressive drugs were administered before the onset of lymph node lesion. However, none of the 9 patients received methotrexate therapy. The present 9 cases were characterized by : (i) prominent lymphoplasmacytic and B-immunoblastic infiltration ; (ii) absence of pronounced arborizing vascular proliferation ; (iii) absence of CD10(+) "clear cells" ; (iv) presence of hyperplastic germinal center in 7 cases ; (v) immunohistochemistry, flow cytometry, and polymerase chain reaction demonstrated a reactive nature of the T- and B-lymphocytes ; and (vi) on in situ hybridization, there were no Epstein-Barr virus -infected lymphoid cells in any of the 9 cases. Overall 5-year survival of our patients was 83%. The combination of clinical, immunophenotypic, and genotypic findings indicated that the present 9 cases can be regarded as having an essentially benign reactive process. Finally, we emphasized that ALPIB should be added to the differential diagnostic problems of atypical LPDs, particularly lymph node lesions of IgG4-related diseases.

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Year:  2010        PMID: 21123969     DOI: 10.3960/jslrt.50.113

Source DB:  PubMed          Journal:  J Clin Exp Hematop        ISSN: 1346-4280


  3 in total

1.  A case of IgG4-related kidney disease complicated by eosinophilic lung disease.

Authors:  Hiroki Adachi; Hiroshi Okuyama; Hideki Yamaya; Nozomu Kurose; Koji Kojima; Hirohisa Toga; Hitoshi Yokoyama
Journal:  CEN Case Rep       Date:  2014-12-16

2.  IgG4-Related Lymphadenopathy.

Authors:  Yasuharu Sato; Tadashi Yoshino
Journal:  Int J Rheumatol       Date:  2012-06-10

3.  Sjögren's syndrome manifesting as clinicopathological features of TAFRO syndrome: A case report.

Authors:  Shino Fujimoto; Hiroshi Kawabata; Nozomu Kurose; Haruka Kawanami-Iwao; Tomoyuki Sakai; Takafumi Kawanami; Yoshimasa Fujita; Toshihiro Fukushima; Yasufumi Masaki
Journal:  Medicine (Baltimore)       Date:  2017-12       Impact factor: 1.817

  3 in total

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