<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Plasma Cell Leukemia on Leukoformula</title><link>https://www.leukoformula.com/en/tags/plazmokletochnyy-leykoz/</link><description>Recent content in Plasma Cell Leukemia on Leukoformula</description><generator>Hugo</generator><language>en-US</language><lastBuildDate>Sat, 19 Mar 2022 15:41:31 +0300</lastBuildDate><atom:link href="https://www.leukoformula.com/en/tags/plazmokletochnyy-leykoz/feed.xml" rel="self" type="application/rss+xml"/><item><title>Primary Plasma Cell Leukemia with Lymphoid-Like Morphology</title><link>https://www.leukoformula.com/en/post/plazmokletochnyy-leykoz-s-limfoidopodobnoy-6862/</link><pubDate>Sat, 19 Mar 2022 15:41:31 +0300</pubDate><guid>https://www.leukoformula.com/en/post/plazmokletochnyy-leykoz-s-limfoidopodobnoy-6862/</guid><description>&lt;p>PLASMA CELL LEUKEMIA WITH “LYMPHOID-LIKE MORPHOLOGY” IN PERIPHERAL BLOOD.
A 59-year-old man with a history of hypertension presented to his doctor with a 1-week history of lower urinary tract symptoms, for which he was prescribed a 7-day course of nitrofurantoin. Given the lack of improvement and the appearance of new non-specific symptoms of malaise, a series of investigations were required.
✅EXAMINATION
Physical examination was unremarkable.
✅COMPLETE BLOOD COUNT:
High white blood cell count (WBC) 43.3 × 10&lt;sup>9/L,
Hemoglobin 104 g/L,
Platelet count 160 × 10&lt;/sup>9 / L.
The automated cell counter (Sysmex XE 2100®, Sysmex Corp) noted lymphocytosis and atypical lymphocytes in the sample.
✅BLOOD SMEAR MICROSCOPY
Peripheral blood (x40, May-Grünwald-Giemsa stain). A monomorphic population of medium-sized mononuclear “lymphoid” cells with abnormal nuclear convolutions, prominent nucleoli, and scanty basophilic cytoplasm, comprising the majority of circulating leukocytes (photo below).
✅BIOCHEMISTRY
In addition to the abnormalities in the complete blood count, the patient had acute kidney injury with creatinine 377 µmol/L (62-106) and urea 19.9 mmol/L (2.5-7.8), hypercalcemia with corrected calcium 3.99 mmol/L (2.2-2.6). Lactate dehydrogenase level was normal.
✅COMPUTED TOMOGRAPHY (CT)
Computed tomography of the neck, chest, pelvis, and abdomen without contrast revealed no enlarged lymph nodes or hepatosplenomegaly; rather widespread osteolytic lesions were noted.
✅IMMUNOPHENOTYPING
Peripheral blood immunophenotyping identified abnormal clonal plasma cells, comprising 66% of total nucleated cells (28.6 × 10^9/L). These cells were positive for CD 38, CD 138, and cytoplasmic kappa and were negative for CD 45, CD 56, and CD 19 (photo below).
✅PROTEIN ELECTROPHORESIS
Accordingly, serum protein electrophoresis was requested, but no monoclonal band was detected, but hypogammaglobulinemia was present. Serum-free light chain analysis showed a kappa free light chain count of 3654.8 mg/L (3.3-19.4) with a kappa/lambda ratio of 589.48. Urine protein electrophoresis identified a free monoclonal kappa light chain band, comprising 76.4% of total urine protein and quantified at 0.44 g/L.
✅CYTOGENETICS
Cytogenetic studies revealed a variant translocation t (11;14) (q13;q32).
✅FINAL DIAGNOSIS
Primary plasma cell leukemia.
✅PROGNOSIS
Primary plasma cell leukemia is a rare and aggressive malignancy.
✅SOURCE
Nesr, Maniusyte, R., Dunlop, A., &amp;amp; Kagdi, H. (2021). Plasma cell leukaemia with “lymphoid‐like morphology” in peripheral blood. International Journal of Laboratory Hematology, 44(1), 10–12. Portico.
✅OUR CONCLUSIONS
Immunophenotyping is the gold standard in diagnosis.&lt;/p></description></item></channel></rss>