Aggressive natural killer-cell neoplasm presenting in the marrow: a report of two cases including one with gains of chromosomes 4q and 9p

被引:2
|
作者
Jhuang, Jie-Yang [1 ]
Clipson, Alexandra [2 ]
Hsieh, Yen-Chuan [3 ]
Yang, Chun-Chieh [3 ,4 ]
Chang, Sheng-Tsung [3 ,5 ]
Du, Ming-Qing [2 ]
Chuang, Shih-Sung [3 ,6 ,7 ]
机构
[1] Far Eastern Mem Hosp, Dept Anat Pathol, New Taipei City, Taiwan
[2] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
[3] Chi Mei Med Ctr, Dept Pathol, Tainan, Taiwan
[4] Chi Mei Med Ctr, Dept Crit Care Med, Tainan, Taiwan
[5] Natl Tainan Inst Nursing, Dept Nursing, Tainan, Taiwan
[6] Natl Taiwan Univ, Dept Pathol, Coll Med, Taipei 10764, Taiwan
[7] Taipei Med Univ, Taipei, Taiwan
来源
DIAGNOSTIC PATHOLOGY | 2015年 / 10卷
关键词
Aggressive natural killer-cell leukemia; Bone marrow; Epstein-Barr virus; Extranodal natural killer/T-cell lymphoma; Primary bone marrow lymphoma; T-cell lymphoma; NASAL-TYPE; BONE-MARROW; LYMPHOMA; LEUKEMIA;
D O I
10.1186/s13000-015-0333-x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aggressive nature killer (NK)-cell neoplasm includes aggressive NK-cell leukemia (ANKL) and extranodal NK/T-cell lymphoma (ENKTL), nasal type. ANKL is rare and is characterized by a systemic neoplastic proliferation of NK-cells, usually with a leukemic presentation. ENKTL is a predominantly extranodal lymphoma, occurring mainly in the upper aerodigestive tract. Both are aggressive neoplasms strongly associated with Epstein-Barr virus (EBV). Here we report two patients with aggressive NK-cells neoplasms localized in the bone marrow (BM) who presented as prolonged fever, anemia, and thrombocytopenia. Both were treated initially as infectious disease. Imaging studies revealed splenomegaly without any nodular lesion or lymphadenopathy. BM examination revealed extensive involvement by EBV-positive NK-cells in both cases. Staging workup including nasal examination/biopsy was negative. Both patients passed away in a month. One case showed gains of chromosomes 4q and 9p by array comparative genomic hybridization. Both tumors were diagnostically challenging due to the unusual clinical presentation and absence of leukemic change, tumor mass or lymphadenopathy. Our cases demonstrate that lymphoma should be considered in patients with fever of unknown origin and bone marrow aspiration/biopsy should be performed as early diagnosis and novel therapeutic regimens may benefit these patients.
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页数:6
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  • [1] Aggressive natural killer-cell neoplasm presenting in the marrow: a report of two cases including one with gains of chromosomes 4q and 9p
    Jie-Yang Jhuang
    Alexandra Clipson
    Yen-Chuan Hsieh
    Chun-Chieh Yang
    Sheng-Tsung Chang
    Ming-Qing Du
    Shih-Sung Chuang
    Diagnostic Pathology, 10
  • [2] LYMPHOPROLIFERATIVE DISORDER OF GRANULAR LYMPHOCYTES - 9 CASES INCLUDING ONE WITH FEATURES OF CD56 (NKH1)-POSITIVE AGGRESSIVE NATURAL-KILLER-CELL LYMPHOMA
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    MODERN PATHOLOGY, 1994, 7 (08) : 819 - 824
  • [3] A T cell lymphoblastic lymphoma patient with two malignant cell populations carrying different 9p deletions including the p16(INK4) and p15(INK4B) genes. Clinical response to interferon-alpha therapy in one of the subclones
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    Nordgren, A
    JeddiTehrani, M
    Rasool, O
    Liu, Y
    Grander, D
    Ost, A
    Wallberg, B
    Johansson, B
    Einhorn, S
    LEUKEMIA, 1996, 10 (05) : 909 - 917