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  1. Article: Heparin-induced thrombocytopenia presenting as splenic hemorrhage following cardiac surgery: a case report.

    Ferry, Joseph / Youssef, Samuel / Wu, Pierce / Hegerova, Livia

    Thrombosis journal

    2021  Volume 19, Issue 1, Page(s) 4

    Abstract: Background: Heparin-induced thrombocytopenia with thrombosis (HITT) is a paradoxical prothrombotic complication of anticoagulant therapy. As many as 3% of patients undergoing cardiac surgery develop clinical HIT presenting as thrombocytopenia with or ... ...

    Abstract Background: Heparin-induced thrombocytopenia with thrombosis (HITT) is a paradoxical prothrombotic complication of anticoagulant therapy. As many as 3% of patients undergoing cardiac surgery develop clinical HIT presenting as thrombocytopenia with or without thrombosis within 5-10 days of heparin exposure. Thrombotic complications associated with HIT carry a mortality rate of 5-10%.
    Case presentation: We report a case of atraumatic splenic hemorrhage due to splenic vein thrombosis as the main indicator of HIT following cardiac surgery in a 62-year-old woman. She presented to the emergency department on day nine following coronary artery bypass graft surgery with acute weakness, dizziness, and malaise. Her evaluation in the emergency department found anemia and thrombocytopenia. A coagulation profile revealed a markedly elevated d-dimer. She underwent a computed tomography scan of the chest, abdomen and pelvis for suspected bleed and was found to have splenic vein thrombosis, right atrial filling defects consistent with atrial thrombus and mild to moderate hemoperitoneum. Surgical consultation was obtained due to splenic hemorrhage. Hematology was consulted on post-operative day 10, however, she unfortunately developed left sided weakness concerning for stroke. A magnetic resonance imaging scan of the brain demonstrated infarct involving distribution of the right anterior cerebral artery. A transesophageal echocardiogram demonstrated a large immobile thrombus within the right atrium with a second, mobile thrombus arising from the left tricuspid valve annulus. Due to a 4Ts score of 7 and markedly positive platelet factor 4 (PF4) IgG antibody a serotonin release assay was not performed given the high probability of HIT. She was cautiously treated with bivalirudin and was transitioned to warfarin anticoagulation. In the following days her platelet count recovered and 3 months later a transthoracic echocardiogram revealed solution of the intracardiac thrombi.
    Conclusions: Atraumatic splenic hemorrhage is an unusual presentation of HIT that is reminiscent of the rare bilateral adrenal hemorrhage due to adrenal necrosis that also occurs in HIT. Alternative anticoagulation is the mainstay of therapy for HIT despite hemorrhage, given the underlying acquired hypercoagulability. Despite similarities of the presentation between splenic hemorrhage and bilateral adrenal hemorrhage, splenic hemorrhage is rarely described in the literature. HIT should be considered in patients presenting with thrombocytopenia following cardiac surgery.
    Language English
    Publishing date 2021-01-19
    Publishing country England
    Document type Journal Article
    ISSN 1477-9560
    ISSN 1477-9560
    DOI 10.1186/s12959-021-00257-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Digital and manual interfollicular Ki-67 are associated with a progression-free survival in patients with low-grade follicular lymphoma.

    Nasir, Aqsa / Hegerova, Livia / Yousaf, Hira / Forster, Colleen L / Shanley, Ryan / Linden, Michael A / Bachanova, Veronika / Yohe, Sophia

    American journal of clinical pathology

    2023  Volume 161, Issue 4, Page(s) 380–387

    Abstract: Objectives: Novel histopathologic prognostic factors are needed to identify patients with follicular lymphoma (FL) at risk of inferior outcomes. Our primary objective was to evaluate the Ki-67 proliferative index in follicular and interfollicular areas ... ...

    Abstract Objectives: Novel histopathologic prognostic factors are needed to identify patients with follicular lymphoma (FL) at risk of inferior outcomes. Our primary objective was to evaluate the Ki-67 proliferative index in follicular and interfollicular areas in tissue biopsy specimens from patients with newly diagnosed FL and correlate with clinical outcomes. Our secondary objective was to correlate PD-L1 and LAG-3 with clinical outcomes.
    Methods: Seventy cases of low-grade FL from the University of Minnesota were evaluated with Ki-67 immunohistochemical stain. Ki-67 expression as a continuous variable was interpreted digitally and manually in follicular and interfollicular areas. Progression-free survival (PFS) and overall survival (OS) were analyzed by Cox regression, and hazard ratios (HRs) per 10-point increase in Ki-67 were calculated.
    Results: Progression-free survival at 4 years was 28% (95% CI, 19%-41%). Interfollicular, but not follicular, Ki-67 was associated with PFS by manual (HR, 1.33; P = .01) and digital (HR, 1.38; P = .02) analysis. Digital and manual Ki-67 were only moderately correlated but demonstrated similar effects on PFS. At 4 years, OS was 90% with no association with follicular or interfollicular Ki-67 proliferation.
    Conclusions: Higher interfollicular Ki-67 by either digital or manual analysis is associated with a poorer PFS in patients with low-grade FL. These results suggest further validation of this marker is warranted to improve pathologic risk stratification at FL diagnosis. PD-L1 and LAG-3 were not associated with PFS or OS.
    MeSH term(s) Humans ; Lymphoma, Follicular/diagnosis ; Lymphoma, Follicular/pathology ; Progression-Free Survival ; Ki-67 Antigen/analysis ; B7-H1 Antigen ; Prognosis ; Disease-Free Survival
    Chemical Substances Ki-67 Antigen ; B7-H1 Antigen
    Language English
    Publishing date 2023-12-04
    Publishing country England
    Document type Journal Article
    ZDB-ID 2944-0
    ISSN 1943-7722 ; 0002-9173
    ISSN (online) 1943-7722
    ISSN 0002-9173
    DOI 10.1093/ajcp/aqad161
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: The ticking heart: a case and review of acute lyme cardiac complications.

    Hegerova, Livia T / Olson, Timothy C

    Minnesota medicine

    2014  Volume 97, Issue 5, Page(s) 42

    MeSH term(s) Adult ; Ambulatory Care ; Diagnosis, Differential ; Doxycycline/therapeutic use ; Electrocardiography ; Female ; Humans ; Lyme Disease/diagnosis ; Lyme Disease/drug therapy ; Myocarditis/diagnosis ; Myocarditis/drug therapy ; Triage
    Chemical Substances Doxycycline (N12000U13O)
    Language English
    Publishing date 2014-05
    Publishing country United States
    Document type Case Reports ; Journal Article ; Review
    ZDB-ID 391068-4
    ISSN 1945-3051 ; 0026-556X
    ISSN (online) 1945-3051
    ISSN 0026-556X
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: A 37-lb tumor.

    Hegerova, Livia T / Chandra, Anupam

    Mayo Clinic proceedings

    2013  Volume 88, Issue 11, Page(s) e135

    MeSH term(s) Aged ; Back/pathology ; Back/surgery ; Diagnosis, Differential ; Female ; Humans ; Lipomatosis, Multiple Symmetrical/diagnosis ; Lipomatosis, Multiple Symmetrical/surgery ; Neoplasms/pathology
    Language English
    Publishing date 2013-11
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 124027-4
    ISSN 1942-5546 ; 0025-6196
    ISSN (online) 1942-5546
    ISSN 0025-6196
    DOI 10.1016/j.mayocp.2013.04.031
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Disseminated histoplasmosis: a cause of hemophagocytic syndrome.

    Hegerova, Livia T / Lin, Yi

    Mayo Clinic proceedings

    2013  Volume 88, Issue 10, Page(s) e123

    MeSH term(s) Adult ; Anemia/diagnosis ; Anemia/etiology ; Anti-Bacterial Agents/therapeutic use ; Anti-Inflammatory Agents/therapeutic use ; Asthma/drug therapy ; Bone Marrow Cells/pathology ; Erythroid Precursor Cells/pathology ; Fever/diagnosis ; Fever/etiology ; Histoplasmosis/complications ; Humans ; Leukopenia/diagnosis ; Leukopenia/etiology ; Liver/physiopathology ; Lymphohistiocytosis, Hemophagocytic/diagnosis ; Lymphohistiocytosis, Hemophagocytic/etiology ; Macrophages/pathology ; Male ; Myeloid Progenitor Cells/pathology ; Phagocytosis/physiology ; Prednisone/therapeutic use ; Thrombocytopenia/diagnosis ; Thrombocytopenia/etiology
    Chemical Substances Anti-Bacterial Agents ; Anti-Inflammatory Agents ; Prednisone (VB0R961HZT)
    Language English
    Publishing date 2013-10
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 124027-4
    ISSN 1942-5546 ; 0025-6196
    ISSN (online) 1942-5546
    ISSN 0025-6196
    DOI 10.1016/j.mayocp.2013.04.030
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Reversal of acquired von Willebrand syndrome with allogeneic stem cell transplant for chronic lymphocytic leukemia.

    Hegerova, Livia / He, Fiona / Zantek, Nicole D / Vercellotti, Gregory M / Holtan, Shernan G / Reding, Mark T

    Blood cells, molecules & diseases

    2019  Volume 77, Page(s) 109–112

    Abstract: Acquired von Willebrand syndrome (AVWS) is a rare, potentially fatal bleeding disorder caused by low activity of von Willebrand factor (VWF) in patients without congenital deficiency. The majority of adult cases are associated with hematological ... ...

    Abstract Acquired von Willebrand syndrome (AVWS) is a rare, potentially fatal bleeding disorder caused by low activity of von Willebrand factor (VWF) in patients without congenital deficiency. The majority of adult cases are associated with hematological malignancy, including lymphoproliferative (48%) or myeloproliferative (15%) disorders (Federici et al., 2000). Both qualitative and quantitative defects occur, due to antibody-mediated clearance or functional interference, increased proteolysis, absorption to malignant cells or platelets, or increased shear stress due to valvular defects or mechanical vascular devices (Tiede et al., 2011). The predominant mechanism for decreased or absent VWF in malignancy is autoantibodies that are inhibitory to VWF function or shorten VWF survival (Kumar et al., 2002 [3]). Antibody-mediated clearance occurs through inactivating antibody directed towards VWF, antibody binding the non-active sites of VWF, and nonspecific antibodies that form circulating immune complexes with VWF, enhancing clearance by the reticuloendothelial system (Mannucci et al., 1984). Bleeding may be very difficult to treat due to reduced half-life of VWF-concentrates.
    MeSH term(s) Adult ; Combined Modality Therapy ; Hematopoietic Stem Cell Transplantation/methods ; Humans ; Leukemia, Lymphocytic, Chronic, B-Cell/complications ; Male ; Plasma Exchange ; Transplantation Chimera ; Transplantation, Homologous ; Treatment Outcome ; von Willebrand Diseases/blood ; von Willebrand Diseases/diagnosis ; von Willebrand Diseases/etiology ; von Willebrand Diseases/therapy ; von Willebrand Factor/metabolism
    Chemical Substances von Willebrand Factor
    Language English
    Publishing date 2019-04-18
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1237083-6
    ISSN 1096-0961 ; 1079-9796
    ISSN (online) 1096-0961
    ISSN 1079-9796
    DOI 10.1016/j.bcmd.2019.04.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: 23-year-old woman with syncope.

    Ball, Caroline A / Hegerova, Livia T / Nkomo, Vuyisile T

    Mayo Clinic proceedings

    2014  Volume 89, Issue 10, Page(s) e93–7

    MeSH term(s) Diagnosis, Differential ; Echocardiography ; Electrocardiography ; Female ; Heart Rate ; Humans ; Magnetic Resonance Imaging, Cine ; Myocarditis/complications ; Myocarditis/diagnosis ; Syncope/diagnosis ; Syncope/etiology ; Syncope/physiopathology ; Tomography, X-Ray Computed ; Young Adult
    Language English
    Publishing date 2014-10
    Publishing country England
    Document type Case Reports ; Journal Article ; Review
    ZDB-ID 124027-4
    ISSN 1942-5546 ; 0025-6196
    ISSN (online) 1942-5546
    ISSN 0025-6196
    DOI 10.1016/j.mayocp.2014.02.021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: 35-year-old man with Fever and abdominal pain.

    Hegerova, Livia T / Swiecicki, Paul L / Kumar, Shaji K

    Mayo Clinic proceedings

    2013  Volume 88, Issue 8, Page(s) 866–870

    MeSH term(s) Abdominal Pain/physiopathology ; Adult ; Anti-Bacterial Agents/administration & dosage ; Anti-Bacterial Agents/classification ; Disease Management ; Fever/physiopathology ; Humans ; Leukemia, Promyelocytic, Acute/blood ; Leukemia, Promyelocytic, Acute/drug therapy ; Male ; Neutropenia/complications ; Neutropenia/etiology ; Neutropenia/physiopathology ; Symptom Assessment/methods ; Treatment Outcome ; Typhlitis/diagnosis ; Typhlitis/drug therapy ; Typhlitis/etiology ; Typhlitis/physiopathology
    Chemical Substances Anti-Bacterial Agents
    Language English
    Publishing date 2013-08
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 124027-4
    ISSN 1942-5546 ; 0025-6196
    ISSN (online) 1942-5546
    ISSN 0025-6196
    DOI 10.1016/j.mayocp.2012.10.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Cold agglutinin disease.

    Swiecicki, Paul L / Hegerova, Livia T / Gertz, Morie A

    Blood

    2013  Volume 122, Issue 7, Page(s) 1114–1121

    Abstract: Cold agglutinin disease is a rare and poorly understood disorder affecting 15% of patients with autoimmune hemolytic anemia. We reviewed the clinical and pathologic features, prognosis, and management in the literature and describe our institutional ... ...

    Abstract Cold agglutinin disease is a rare and poorly understood disorder affecting 15% of patients with autoimmune hemolytic anemia. We reviewed the clinical and pathologic features, prognosis, and management in the literature and describe our institutional experience to improve strategies for accurate diagnosis and treatment. Retrospective analysis identified 89 patients from our institution with cold agglutinin disease from 1970 through 2012. Median age at symptom onset was 65 years (range, 41 to 83 years), whereas the median age at diagnosis was 72 years (range, 43 to 91 years). Median survival of all patients was 10.6 years, and 68 patients (76%) were alive 5 years after the diagnosis. The most common symptom was acrocyanosis (n = 39 [44%]), and many had symptoms triggered by cold (n = 35 [39%]) or other factors (n = 20 [22%]). An underlying hematologic disorder was detected in 69 patients (78%). Thirty-six patients (40%) received transfusions during their disease course, and 82% received drug therapy. Rituximab was associated with the longest response duration (median, 24 months) and the lowest proportion of patients needing further treatment (55%). Our institution's experience and review of the literature confirms that early diagnostic evaluation and treatment improves outcomes in cold agglutinin disease.
    MeSH term(s) Anemia, Hemolytic, Autoimmune/diagnosis ; Anemia, Hemolytic, Autoimmune/therapy ; Disease Management ; Humans ; Prognosis ; Retrospective Studies
    Language English
    Publishing date 2013-06-11
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 80069-7
    ISSN 1528-0020 ; 0006-4971
    ISSN (online) 1528-0020
    ISSN 0006-4971
    DOI 10.1182/blood-2013-02-474437
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  10. Article: An insidious cardiac sarcoma presenting with progressive neurologic dysfunction.

    Pasalic, Dario / Hegerova, Livia T / Gonsalves, Wilson I / Robinson, Steven

    Rare tumors

    2013  Volume 5, Issue 4, Page(s) e56

    Abstract: Central nervous system metastases as the presentation of primary cardiac sarcoma are a very rare entity, with only a few previously reported cases. Sarcomas specifically make up 10 to 20% of all primary cardiac tumors. Patients with primary cardiac ... ...

    Abstract Central nervous system metastases as the presentation of primary cardiac sarcoma are a very rare entity, with only a few previously reported cases. Sarcomas specifically make up 10 to 20% of all primary cardiac tumors. Patients with primary cardiac tumors typically present with cardiac symptomatology that may include arrhythmias, obstruction to blood flow and valve function, or symptoms of heart failure. We report a unique case of a patient with a primary cardiac sarcoma who presented with progressive neurologic dysfunction secondary to brain metastases without any preceding cardiac symptoms. We describe our novel management of these unique cases and discuss the current medical and surgical approaches to treating neurologic metastases from cardiac sarcoma.
    Language English
    Publishing date 2013-10-18
    Publishing country England
    Document type Case Reports
    ZDB-ID 2514363-3
    ISSN 2036-3613 ; 2036-3605
    ISSN (online) 2036-3613
    ISSN 2036-3605
    DOI 10.4081/rt.2013.e56
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