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- W2093409927 abstract "Primary lymphoma of bone (PLB) is an uncommon bone tumour with a relatively homogenous morphology and unusual clinical behaviour [1, 2]. It is defined as lymphoma arising from bone without evidence of any extraskeletal involvement at the time of presentation. An interval of 4–6 months from the time of the osseous lesion to the development of the extraskeletal disease is required to consider a PLB by some investigators [1–3]. This is one of the rare cause of primary osteolytic lesion [1].Primary non-hodkins lymphoma (NHL) of bone comprises approximately 4–5 % of all extranodal NHL. Since, PLB is a curable disease, it should be differentiated from other lytic bone lesions such as secondaries and other primary bone tumours [2–4]. Due to its rarity, only a few retrospective studies have been published addressing the prognosis and treatment of PLB. Most of the studies had small patient numbers retrospectively collected over a long time span, resulting in a heterogeneous group of patients with different staging methods and a great diversity of treatment approaches [1, 3, 4]. Diagnosis of nodal lymphomas on Fine needle aspiration cytology (FNAC) has been well established. However, cytodiagnosis of primary lymphoma of bone has not been well documented because of its rarity [3]. We report a case of primary bone lymphoma involving proximal humerus in a 31-year old male diagnosed by FNAC, later confirmed by histopathology and immunohistochemistry." @default.
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- W2093409927 date "2013-07-17" @default.
- W2093409927 modified "2023-09-26" @default.
- W2093409927 title "Primary Bone Lymphoma of Humerus Diagnosed by FNAC- A Rare Case Report" @default.
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- W2093409927 doi "https://doi.org/10.1007/s13193-013-0251-x" @default.
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