S112 © American Society for Clinical Pathology
AJCP / Meeting AbstrActs
Am J Clin Pathol 2018;150:S93-S115
DOI: 10.1093/AJCP/AQY097
patients with HM who had peripheral blood fow cyto-
metric (PBFC) tests, seven cases were positive for atyp-
ical/neoplastic populations concordant with the fnal
diagnosis either in bone marrow or tissue, whereas none
of fve non-HM cases were positive. The sensitivity and
specifcity of PBFC to predict HM were 78% and 100%,
respectively. The percentage of the neoplastic population
ranged from 0.55% to 92% and was higher in one case of
acute myeloid leukemia. The immunophenotypic profle,
including large cell size, was suffciently aberrant to distin-
guish from indolent clonal lymphocytosis.
Conclusion: Our study demonstrated the predictive power
of PBFC for diagnosing hematolymphoid malignancy in
HLH patients with a high sensitivity and specifcity. We
recommend PBFC (with a STAT result available in hours)
to be used as an initial screening test in cases where there is
high clinical suspicion for HLH and HM followed by con-
frmatory tissue diagnosis. This process may aid in a timely
diagnosis and treatment to improve the clinical outcomes.
Epstein-Barr Virus, Human Herpesvirus 8, and Human
T-Lymphotropic Virus Type 1 Infections Amongst
Patients With Lymphoid Malignancies: Exploring Causal
Relationship, in Calabar
Bassey Bassey, MB, BCH,
1
Marcus Asuquo, MD,
FMCPath,
1
and Alani Akanmu, FMCPath
2
;
1
University
of Calabar Teaching Hospital and
2
Lagos University
Teaching Hospital
Objectives: To determine the prevalence of EBV/HHV-8/
HTLV-1 among patients with LM and compare with con-
trols. To determine the relationship between history of
blood transfusion, socioeconomic data, and blood indices
with positivity of oncogenic viruses.
Methods: A total of 180 participants who gave informed
consent were recruited, 60 with LM and 120 controls.
Socioeconomic data and history of blood transfusion were
obtained through questionnaire. Ten milliliters of blood was
collected from each patient: 5 mL into EDTA for FBC and
5 mL into a plain bottle for ELISA to test for oncogenic
viruses.
Results: LM population had EBNA IgG prevalence of
76.7%, while controls had 75.0% (P = .806). EBNA IgM
prevalence for LM patients and controls was no different
from each other (8.3%) (P = 1.000). HHV-8 prevalence for
LM patients had 5% while controls had 11.7% (P = .149).
None (0%) of the study participants was positive for HTLV-
1. Participants who had never received a blood transfusion
had 75.7% positivity for EBNA IgG, 9.3% for EBNA IgM,
and 10% for HHV-8. Those transfused had 75% positivity
for EBNA IgG, 5% for EBNA IgM, and 7.5% for HHV-8
(EBNA IgG, P = .926; EBNA IgM, P = .387; and HHV-8,
P = .633). Concerning only patients with LM, 30 (65.2%)
positive for EBNA IgG had received blood while 16 (34.8%)
had not (P = .666). Two (40%) positive for EBNA IgM had
received blood while three (60%) had not (P = .186). The
three patients who were positive for HHV-8 had received a
blood transfusion. There were statistically signifcant dif-
ferences between the various blood indices of LM patients
and the controls (P < .05), except MCH, which was not
signifcant (P = .115). There was no statistically signifcant
difference between the socioeconomic data of LM patients
who were infected with the oncogenic viruses and those
who were not (P > .05).
Conclusion: The study shows that oncogenic viruses are
not frequently associated with LM in Calabar, and blood
transfusion does not incur any additional risk.
Plasma Cell Neoplasms (PCNs) With Low-Risk,
Favorable Gene Expression Subtypes Are More Often
Associated With Therapy-Related Myelodysplastic
Syndrome (t-MDS)
Anwar Rjoop, MD, Rodolfo Henrich Lobo, MD,
Soumya Pandey, MD, and Daisy Alapat, MD; University
of Arkansas for Medical Sciences
Objectives: t-MDS are clonal hematopoietic disorders
that develop secondary to chemotherapy and/or radiation
therapy. Prior studies have shown a complex karyotype
and abnormalities involving chromosomes 5 and 7 in
PCN patients developing t-MDS. However, these abnor-
malities can be seen in both de novo MDS and t-MDS,
and it can sometimes be challenging to differentiate mul-
tiple myeloma/MDS signature from t-MDS. This study
was performed to identify patterns of gene expression
profling (GEP) and any novel karyotypic abnormalities
in newly diagnosed t-MDS in patients with a history of
treated PCNs.
Methods: A retrospective review was performed to iden-
tify any new diagnosis of t-MDS on bone marrow exam-
ination in all patients undergoing treatment at UAMS
for PCNs during 2014 to 2016. Thirty-four patients were
identifed. Additional data were collected, including GEP
based on our previously published UAMS protocol,
karyotype analysis, and myeloid mutational profle using
NextGen sequencing.
Results: GEP analysis showed a low-risk gene class
with favorable prognosis in the majority of the patients
(26/34, 84%). On GEP subgroup analysis, hyperdiploid
(HY) and cyclin D2 (CD2) (10 in each category, 31%)
were most commonly seen. Abnormalities of chromo-
somes 5 (10/34; 29%) and/or 7 (8/34; 23%) and a complex
karyotype (28/34; 82.3%) were noted in a majority of the
patients, similar to prior studies. In addition, we observed
an unbalanced dicentric translocation dic(5;17) (q11;p11)
in ~29% patients. NGS analysis performed on a subset
of the patients revealed TP53 as the most common gene
mutation (81%).
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