Primary Plasma Cell Leukaemia: Case report and review of the literature

Plasma cell leukaemia (PCL) is one of the most aggressive and rarest forms of plasma cell dyscrasia. However, the diagnostic criteria for this condition have not yet been revised and there is no specific treatment to significantly improve the course of the disease. We report a 69-year-old male who p...

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Main Authors: Sarika Singh, Ashutosh Rath, Surekha Yadav
Format: Article
Language:English
Published: Sultan Qaboos University 2018-12-01
Series:Sultan Qaboos University Medical Journal
Online Access:https://journals.squ.edu.om/index.php/squmj/article/view/2868
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author Sarika Singh
Ashutosh Rath
Surekha Yadav
author_facet Sarika Singh
Ashutosh Rath
Surekha Yadav
author_sort Sarika Singh
collection DOAJ
description Plasma cell leukaemia (PCL) is one of the most aggressive and rarest forms of plasma cell dyscrasia. However, the diagnostic criteria for this condition have not yet been revised and there is no specific treatment to significantly improve the course of the disease. We report a 69-year-old male who presented to the Lok Nayak Hospital, New Delhi, India, in 2017 with dyspnoea and chest pain. A peripheral blood smear showed an absolute plasma cell count of 2.16 × 109/L. A bone marrow examination showed 61% atypical plasma cells exhibiting kappa light chain restriction. Biochemical investigations were consistent with a diagnosis of primary PCL with renal involvement. Bortezomib-based chemotherapy was initiated, which resulted in an improvement in the patient’s haematological and biochemical parameters. This case report includes a comprehensive review of the clinical and diagnostic features, pathobiology and treatment of PCL. Keywords: Plasma Cell Leukemia; Multiple Myeloma; Plasma Cells; Case Report; India.
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spelling doaj.art-a9e5ba74c22c498fa13e4067de536dfc2022-12-22T01:58:05ZengSultan Qaboos UniversitySultan Qaboos University Medical Journal2075-051X2075-05282018-12-0118339740110.18295/squmj.2018.18.03.0242473Primary Plasma Cell Leukaemia: Case report and review of the literatureSarika Singh0Ashutosh Rath1Surekha Yadav2Department of Pathology, Maulana Azad Medical College, New Delhi, IndiaDepartment of Pathology, Maulana Azad Medical College, New Delhi, IndiaDepartment of Pathology, Maulana Azad Medical College, New Delhi, IndiaPlasma cell leukaemia (PCL) is one of the most aggressive and rarest forms of plasma cell dyscrasia. However, the diagnostic criteria for this condition have not yet been revised and there is no specific treatment to significantly improve the course of the disease. We report a 69-year-old male who presented to the Lok Nayak Hospital, New Delhi, India, in 2017 with dyspnoea and chest pain. A peripheral blood smear showed an absolute plasma cell count of 2.16 × 109/L. A bone marrow examination showed 61% atypical plasma cells exhibiting kappa light chain restriction. Biochemical investigations were consistent with a diagnosis of primary PCL with renal involvement. Bortezomib-based chemotherapy was initiated, which resulted in an improvement in the patient’s haematological and biochemical parameters. This case report includes a comprehensive review of the clinical and diagnostic features, pathobiology and treatment of PCL. Keywords: Plasma Cell Leukemia; Multiple Myeloma; Plasma Cells; Case Report; India.https://journals.squ.edu.om/index.php/squmj/article/view/2868
spellingShingle Sarika Singh
Ashutosh Rath
Surekha Yadav
Primary Plasma Cell Leukaemia: Case report and review of the literature
Sultan Qaboos University Medical Journal
title Primary Plasma Cell Leukaemia: Case report and review of the literature
title_full Primary Plasma Cell Leukaemia: Case report and review of the literature
title_fullStr Primary Plasma Cell Leukaemia: Case report and review of the literature
title_full_unstemmed Primary Plasma Cell Leukaemia: Case report and review of the literature
title_short Primary Plasma Cell Leukaemia: Case report and review of the literature
title_sort primary plasma cell leukaemia case report and review of the literature
url https://journals.squ.edu.om/index.php/squmj/article/view/2868
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