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Follicular dendritic cell tumor as an unknown primary tumor
Authors:Yoshihiro Yakushijin  Hisaharu Shikata  Katsumi Kito  Kohichi Ohshima  Kensuke Kojima  Takaaki Hato  Hitoshi Hasegawa  Masaki Yasukawa
Affiliation:(1) Department of Bioregulatory Medicine, Ehime University Graduate School of Medicine, Tohon-shi, Ehime 791-0295, Japan;(2) Department of Molecular Pathology, Ehime University Graduate School of Medicine, Ehime, Japan;(3) Department of Pathology, Kurume University School of Medicine, Fukuoka, Japan
Abstract:A 70-year-old Japanese man presented to our hospital with a 1-month history of progressive general fatigue and anorexia. A physical examination revealed severe anemic condition, mild persistent splenomegaly, and no palpable surface lymph nodes. He had pleural effusion and ascites, though no malignant cells were detected in the effusion. He eventually died without any diagnosis of his disease. Immunohistochemical staining of his tumor after autopsy showed atypical cells that were negative for epithelial membrane antigen (EMA), keratin (AE1/3), keratin-20, vimentin, factor VIII, leukocyte common antigen (LCA/T200; CD45), myeloperoxidase (MPO), terminal deoxynucleotidyl tranferase (TdT), lysozyme, CD1a, CD3, CD4, CD10, CD15, CD20 (L26), CD21, CD23, CD34, CD43, CD56, CD68, CD79a, CD138, and EBER-1 in situ. Only a few scattered cells expressed CD30, but they showed no staining for anaplastic large-cell lymphoma kinase (ALK). A few scattered cells expressed S-100 antigen and the majority of cells dominantly expressed dendritic cell-associated antigens (CD35, FDC, Ki-M1p). In conclusion, we found this unknown primary tumor to be consistent with a follicular dendritic cell tumor with anaplastic features.
Keywords:Unknown primary tumor  Primary lymph node neoplasm  Follicular dendritic cell tumor
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