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Letter to the Editors
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| Plasma cell leukemia of IgG secreting type: A rare case | ||||||
| Parth Desai1, Sagar Dholariya2, Sanjeev Gupta3, Tejinder Singh4 | ||||||
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1MBBS, Resident Department of Pathology, MAMC, Maulana Azad Medical College, New Delhi.
2MBBS, Resident Department of Biochemistry, MAMC, Maulana Azad Medical College, New Delhi. 3DM Hematopathology, Professor AIIMS, Maulana Azad Medical College, New Delhi. 4MD Pathology, Director Professor, MAMC, Maulana Azad Medical College, New Delhi. | ||||||
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| How to cite this article: |
| Desai PA, Dholariya S, Gupta S, Singh T. Plasma cell leukemia of IgG secreting type: A rare case. International Journal of Case Reports and Images 2013;4(12):748–749. |
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Letter to the Editor
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Plasma cell leukemia is very rare comprising 2% plasma cell dyscrasias. [1] We report a case of a 49-year-old male with complaints of chest pain, breathlessness, and acute attacks of gastroenteritis. On examination, there was marked pallor and hepatosplenomegaly. X-ray and computed tomography (CT) scan revealed multiple paratracheal lymph node enlargements. However, there was no diffuse osteopenia or multiple osteolytic lesions. Laboratory analysis revealed high serum calcium 11.5 mg/dL, low hemoglobin 5 g/dL, normal WBC count, thrombocytopenia 22000/mm3 and elevated erythrocyte sedimentation rate (ESR). Peripheral smear showed many atypical cells (41%) with blastoid morphology, giving a blood picture of acute leukemia. However, on closer inspection many of them appeared plasmacytoid. There was marked rouleaux formation of red cells in the background. Bone marrow aspirate and biopsy also revealed near total replacement by such atypical cells with plasmacytoid morphology. Serum electrophoresis revealed a prominent M spike and immunofixation revealed IgG heavy chain and kappa light chain immunostaining ruling out the possibility of Waldenström’s macroglobulinemia. Plasma cell leukemias are predominantly IgD and IgE secreting type. [2] [3] [4] This case is rare in that it is IgG secreting type. Plasma cell leukemias are very aggressive and with higher incidence of organomegaly, lymphadenopathy, thrombocytopenia, hypercalcemia, renal impairment and surprisingly lesser occurrence of lytic bony lesions as in our case. [1] [2][4] |
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Author Contributions:
Parth Anil Desai – Substantial contributions to conception and design, Acquisition of data, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published Sagar Dholariya – Substantial contributions to conception and design, Acquisition of data, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published Sanjeev Gupta – Substantial contributions to conception and design, Acquisition of data, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published Tejinder Singh – Substantial contributions to conception and design, Acquisition of data, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published |
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Guarantor of submission
The corresponding author is the guarantor of submission. |
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Source of support
None |
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Conflict of interest
Authors declare no conflict of interest. |
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Copyright
© Parth Anil Desai et al. 2013; This article is distributed the terms of Creative Commons Attribution License which permits unrestricted use, distribution and reproduction in any means provided the original authors and original publisher are properly credited. (Please see Copyright Policy for more information.) |
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