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Loaiza-Bonilla A, Horowitz D, Sheela S, et al. Persistent Tn polyagglutination syndrome during febrile neutropenia: a case report and review of the literature. J Med Case Rep. 2011;5:8doi: 10.1186/1752-1947-5-8.
Loaiza-Bonilla, A., Horowitz, D., Sheela, S., Baral, A., Tinoco, G., & Kyriakopoulos, C. (2011). Persistent Tn polyagglutination syndrome during febrile neutropenia: a case report and review of the literature. Journal of medical case reports, 58. https://doi.org/10.1186/1752-1947-5-8
Loaiza-Bonilla, Arturo, et al. "Persistent Tn polyagglutination syndrome during febrile neutropenia: a case report and review of the literature." Journal of medical case reports vol. 5 (2011): 8. doi: https://doi.org/10.1186/1752-1947-5-8
Loaiza-Bonilla A, Horowitz D, Sheela S, Baral A, Tinoco G, Kyriakopoulos C. Persistent Tn polyagglutination syndrome during febrile neutropenia: a case report and review of the literature. J Med Case Rep. 2011 Jan 14;5:8. doi: 10.1186/1752-1947-5-8. PMID: 21235740; PMCID: PMC3025968.
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J Med Case Rep. 2011 Jan 14;5:8. doi: 10.1186/1752-1947-5-8.

Persistent Tn polyagglutination syndrome during febrile neutropenia: a case report and review of the literature.

Journal of medical case reports

Arturo Loaiza-Bonilla, Daniel Horowitz, Sheenu Sheela, Anupa Baral, Gabriel Tinoco, Christos Kyriakopoulos

Affiliations

  1. The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, Maryland 21287, USA. [email protected].

PMID: 21235740 PMCID: PMC3025968 DOI: 10.1186/1752-1947-5-8

Abstract

INTRODUCTION: Tn polyagglutination syndrome is a rare disorder that has been reported on only a few occasions in the literature, and, to the best of our knowledge, never before in the context of febrile neutropenia.

CASE PRESENTATION: We report the case of a 26-year-old Caucasian woman who presented to our emergency department complaining of a persistent fever over the previous three days. She had a history of long-standing refractory pancytopenia with multi-lineage dysplasia and severe neutropenia, but she had rarely experienced infection. The results of a physical examination and multiple laboratory tests were unremarkable. While investigating the possible causes of the refractory, long-standing pancytopenia, the possibility of a polyagglutinable state was suggested. Blood samples were sent to the laboratory for an analysis of mixed-field seed lectin agglutination assay. A serum lectin panel confirmed the final diagnosis of Tn-activation.

CONCLUSIONS: We should include Tn-activation in our differential whenever we encounter cases of refractory long-standing idiopathic cytopenias and inconclusive bone marrow results displaying multi-lineage dysplasia. Novel genetic techniques have recently revealed the interesting pathophysiology of this phenomenon. The recognition and inclusion of Tn polyagglutination syndrome in our differential diagnoses has important clinical implications, given its main associated features, such as severe thrombocytopenia and neutropenia, which are usually linked to a benign clinical course and prognosis. Increased awareness of the polyagglutinable disorders will potentially decrease the need for invasive and costly medical interventions and also raises the need for monitoring of this specific sub-set of patients. In addition, the study of the expression and implications of Tn, and other similar antigens, offers a fascinating perspective for the study of its role in the diagnosis, prognosis and immunotherapy of solid tumors and hematological malignancies. The infrequency with which Tn polyagglutination syndrome is encountered, its clinical features and its pathophysiology make it a formidable diagnostic challenge.

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