Journal Basic Info

  • Impact Factor: 2.709**
  • H-Index: 11 
  • ISSN: 2474-1663
  • DOI: 10.25107/2474-1663
**Impact Factor calculated based on Google Scholar Citations. Please contact us for any more details.

Major Scope

  •  Blood Cancer
  •  Kidney Cancer
  •  Radiation Therapy
  •  Thoracic Oncology
  •  Prostate Cancer
  •  Paediatric Cancers
  •  Adjuvant Therapy
  •  Surgical Oncology

Abstract

Citation: Clin Oncol. 2017;2(1):1273.DOI: 10.25107/2474-1663.1273

Primary Lymphoma of the Sacrum- A Rare Entity

Amol Dilip Amonkar, Boney Perumal, Bhaskar Mallaiah, Fayiza Musthafa

Department of Lymphoma, KIMS Hospital and Research Centre, Bengaluru, India

*Correspondance to: Bhaskar Mallaiah 

 PDF  Full Text Case Report | Open Access

Abstract:

Primary lymphomas of the bone are rare neoplasm accounting for approximately 0.4% of all primary bone tumours. We report a case of 39 year old male who presented with lower backache. Computed Tomography (CT) showed a mixed sclerotic and osteolytic lesion involving predominantly the right half of sacrum with adjacent soft tissue and muscle thickening and enlarged regional lymph nodes, mimicking a sacral neoplasm. Histology of the lymph node showed features of non-Hodgkins lymphoma, immunohistochemistry confirmed the diagnosis. The patient underwent radiotherapy followed by chemotherapy (CHOP Regimen). A diagnosis of primary lymphoma of the sacrum was made as it fulfils the criteria of primary lymphoma of the bone (PBL) that is involvement of a single skeletal site with or without regional lymph node involvement. To the best of our knowledge, primary lymphoma of the sacrum is an extremely rare condition and only a handful of cases are reported till date. We report a case of primary lymphoma of the sacrum with relevant discussion on the same.

Keywords:

Primary bone lymphoma; Non-Hodgkins lymphoma; Sacrum; Diffuse large B cell lymphoma; Immunohistochemistry

Cite the Article:

Amonkar AD, Perumal B, Mallaiah B, Musthafa F. Primary Lymphoma of the Sacrum- A Rare Entity. Clin Oncol. 2017; 2: 1273.

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