Platelet Satellitism Causing Apparent Loss of Response to Eltrombopag in a Patient With Immune Thrombocytopenia

A 12-year-old patient was diagnosed with immune thrombocytopenia. Following an inadequate response to corticosteroids, intravenous immunoglobulin and romiplostim, treatment was switched to eltrombopag, which led to stabilization of platelet counts. After 4 months of stable platelet counts above 100x103/μL, an automated complete blood count (CBC) performed on an ethylenediaminetetraacetic acid (EDTA)-anticoagulated sample showed a sudden platelet drop to 80x103/μL, prompting the suspicion of loss of response to the oral thrombopoietin receptor agonist. Review of the peripheral blood smear showed characteristic pictures of platelet satellitism (Figure 1,A–C). In approximately 30% of the involved polymorphonuclear neutrophils, platelet phagocytosis was also apparent (Figure 1,D–F). A spurious thrombocytopenia due to platelet satellitism was suspected, and a microscopic estimation of platelet count—considering even the platelets adhering to neutrophils' membrane or detectable within granulocytes' cytoplasm—yielded a result consistent with prior counts (120–140 x103/μL). The occurrence of platelet satellitism was subsequently confirmed exclusively in blood slides prepared from EDTA- (Figure 1,G), and not from citrate- (Figure 1,H) or lithium heparin-anticoagulated sample (Figure 1,I). Platelet satellitism is an EDTA-associated in vitro phenomenon with much lower incidence than the “classical” EDTA-dependent pseudothrombocytopenia, which causes false thrombocytopenia due to platelet agglutination. Its recognition still requires microscopic assessment of the blood smear [1, 2]. A noticeable spuriously reduced platelet count due to satellitism is exceptionally rare [3] but should be considered when there is an unexpected result, as illustrated in this case. T.E., S.H., and L.B.K. collected clinical information. T.E. and C.Z. performed and interpreted blood films assessment by light microscopy. C.Z. wrote the manuscript. All authors helped with data interpretation, critically reviewed the manuscript, and approved the final version. The authors have nothing to report. The authors have nothing to report. The authors have nothing to report. The authors declare no conflicts of interest. The data that support the findings of this study are available from the corresponding author upon reasonable request.

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Publication Details

Journal
International Journal of Laboratory Hematology
Published
2026-02-16
DOI
https://doi.org/10.1111/ijlh.70071
Primary Topic
Clinical Laboratory Practices and Quality Control
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article
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article

Platelet Satellitism Causing Apparent Loss of Response to Eltrombopag in a Patient With Immune Thrombocytopenia

Carlo Zaninetti, Torsten Ebeling, Stefanie Huber
International Journal of Laboratory Hematology
Clinical Laboratory Practices and Quality Control
article

Platelet Satellitism Causing Apparent Loss of Response to Eltrombopag in a Patient With Immune Thrombocytopenia

Carlo Zaninetti, Torsten Ebeling, Stefanie Huber
article en

Abstract

A 12-year-old patient was diagnosed with immune thrombocytopenia. Following an inadequate response to corticosteroids, intravenous immunoglobulin and romiplostim, treatment was switched to eltrombopag, which led to stabilization of platelet counts. After 4 months of stable platelet counts above 100x103/μL, an automated complete blood count (CBC) performed on an ethylenediaminetetraacetic acid (EDTA)-anticoagulated sample showed a sudden platelet drop to 80x103/μL, prompting the suspicion of loss of response to the oral thrombopoietin receptor agonist. Review of the peripheral blood smear showed characteristic pictures of platelet satellitism (Figure 1,A–C). In approximately 30% of the involved polymorphonuclear neutrophils, platelet phagocytosis was also apparent (Figure 1,D–F). A spurious thrombocytopenia due to platelet satellitism was suspected, and a microscopic estimation of platelet count—considering even the platelets adhering to neutrophils' membrane or detectable within granulocytes' cytoplasm—yielded a result consistent with prior counts (120–140 x103/μL). The occurrence of platelet satellitism was subsequently confirmed exclusively in blood slides prepared from EDTA- (Figure 1,G), and not from citrate- (Figure 1,H) or lithium heparin-anticoagulated sample (Figure 1,I). Platelet satellitism is an EDTA-associated in vitro phenomenon with much lower incidence than the “classical” EDTA-dependent pseudothrombocytopenia, which causes false thrombocytopenia due to platelet agglutination. Its recognition still requires microscopic assessment of the blood smear [1, 2]. A noticeable spuriously reduced platelet count due to satellitism is exceptionally rare [3] but should be considered when there is an unexpected result, as illustrated in this case. T.E., S.H., and L.B.K. collected clinical information. T.E. and C.Z. performed and interpreted blood films assessment by light microscopy. C.Z. wrote the manuscript. All authors helped with data interpretation, critically reviewed the manuscript, and approved the final version. The authors have nothing to report. The authors have nothing to report. The authors have nothing to report. The authors declare no conflicts of interest. The data that support the findings of this study are available from the corresponding author upon reasonable request.

International Journal of Laboratory Hematology
Universitätsmedizin Greifswald (DE)
Openalex Percentile: Top 50%
Clinical Laboratory Practices and Quality Control
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