Circulating red cell mass in polycythemia vera as determined by red blood cells tagged with the radio-active isotope of iron

1949 ◽  
Vol 7 (2) ◽  
pp. 254-255
Author(s):  
George R. Meneely ◽  
E.B. Wells ◽  
Paul F. Hahn
2020 ◽  
Vol 13 (2) ◽  
pp. 578-582
Author(s):  
Ahmed M. Abdalhadi ◽  
Mohamed A. Yassin

Polycythemia vera is one of the myeloproliferative neoplasms that is distinguished by the uncontrolled production of blood cells and an increased red cell mass due to acquired JAK2 mutation. It has many complications and it might increase the risk of other tumors. However, it does not cause hypercalcemia and is rarely associated with parathyroid adenoma. Here, we report on a 64-year-old female with polycythemia vera found to have hypercalcemia due to parathyroid adenoma.


Acta Andina ◽  
2014 ◽  
Vol 9 (1-2) ◽  
pp. 68
Author(s):  
Clarence P. Alfrey ◽  
Lawrence Rice

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Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 1581-1581
Author(s):  
Tiziano Barbui ◽  
Jürgen Thiele ◽  
Heinz Gisslinger ◽  
Guido Finazzi ◽  
Alessandra Carobbio ◽  
...  

Abstract Introduction Patients with masked polycythemia vera (mPV) present with hemoglobin (HB) values borderline inferior to those required by the World Health Organization (WHO) diagnostic criteria (HB >16.5g% and >18.5 g% in female and male respectively) but are suspected to have PV for presenting clinico-hematological features. The diagnostic HB values required by the WHO guidelines have been considered surrogate of increased red cell mass (RCM). However, in both males and females HB values are not always equal to an absolute erythrocytosis and conversely a HB concentration below the required cut off level could be associated with an increased red cell mass. We believe that bone marrow (BM) morphology may play an important role in differentiating PV from other MPN entities and reactive changes. In this study we investigated JAK2V617/Exon12-positive patients showing BM features characteristic for PV and classified as mPV or overt PV according to their hemoglobin levels and evaluated their respective outcomes including thrombosis, progression to myelofibrosis (MF), acute leukemia (AL) and overall survival with the purpose to support the diagnosis of PV also in patients presenting with lower HB levels than required by WHO criteria. Materials and Methods A clinicopathological database of patients who were diagnosed and treated for PV was created by clinicians and hematopathologists from seven international centers of excellence for MPNs. Eligibility criteria for entry included the presence of JAK2V617F (or Exon12) mutation, EPO measurement, no evidence of subnormal ferritin levels and the availability of representative, treatment-naive BM biopsies (hematoxylin-eosin staining and silver impregnation after Gomori or Gordon-Sweet). All BM biopsies were centrally re-reviewed by one of the authors (J.T.) who was completely blinded to outcome data. In both mPV and overt PV patients, phlebotomy and cytoreductive therapy were used with the same frequency (p=0.101). Results and Discussion Among 397 mutated patients, with PV BM morphology as defined by WHO, 257 (65%) met the full WHO-2008 criteria. The remaining 140 patients (35%) were classified as mPV for levels of HB at diagnosis, ranging from 16.5 to 18.5 g/dL in men and from 15.0 to 16.5 g/dL in women, and frequent presence of subnormal EPO levels (65%). At baseline, mPV patients were more males, had more previous arterial thrombosis and presented more frequently with platelet counts exceeding the required level of WHO-defined ET (450 x 109/L), often mimicking clinically this entity at onset. After a median follow-up of 3.8 (0-29.8) and 4.5 (0-21.1) years in mPV and overt PV, respectively, time to the first thrombotic event was superimposable in the two groups while time to progression to MF and AL was significantly different .These combined events were recorded in 10% of mPV and 5.8% of overt PV, corresponding to an annual rate of 1.60 % pts/year in mPV and 0.97 % pts/year in overt PV, respectively (p=0.010). In addition, an inferior overall survival was documented in mPV patients in comparison with overt PV (p=0.011). The annual rate of death in mPV was almost twice that of overt PV, mainly due to an excess of hematological transformation (overt MF and AL). Multivariable analysis identified age older than 65 years (hazard ratio (HR) 6.63, P<.0001), WBC >10 x109/L (HR 2.99, P=.005) and diagnosis of mPV (HR 2.38, P=.036) as independent risk factors for survival in these patients. These results show that in JAK2 mutated patients with borderline HB levels, BM features may be a valid support to confirm the suspicion of PV diagnosis. Of interest, recent data demonstrated that all patients with increased RCM also had BM morphology typical of PV. It is tempting to speculate that the clinico-hematologic phenotype of mPV may represent an early stage of a JAK2 mutated MPN, presenting as a variant of PV, with a more rapid progression to MF and AL. The recognition of these early PV patients has an important clinical impact since, in spite of not meeting the full WHO criteria, mPV share the same vascular risk as overt PV. In conclusion, these data suggest that mPV is not necessarily only an early form of classical PV but a distinct entity with disease outcomes akin to primary myelofibrosis. Disclosures: No relevant conflicts of interest to declare.


Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 5249-5249 ◽  
Author(s):  
Hassan A. Al-Jafar ◽  
Leena M Aytoglu ◽  
Issa Loutfi ◽  
Iman Al-Shemmari ◽  
Salem H Alshemmari

Abstract Introduction In Polycythaemia Vera (PV), the RBC lineage is involved with increased haemoglobin, RBC count and haematocrit. WHO diagnostic criteria for PV are JAK2 V617F mutation and elevated red cell mass (RCM) > 25% of mean normal value. In addition, tests of marrow hypercellularity, blood erythropoietin and colony formation, are minor criteria. However, the diagnostic role of RCM test is still controversial and requires clarification. In this work, PV patients who had both an RCM study and JAK2 V617F mutation test, and routine laboratory tests, are evaluated to check if RCM was essential in the diagnostic work up for PV. Methods Over 2 years, 75 patients with abnormal haematocrit (men ≥ 0.50, women ≥ 0.45) had RCM and JAK2 V617F mutation tests (except JAK2 exon 12 mutation). All subjects consented to the study approved by the ethics committee. RCM was done by Cr-51 RBC radiolabeling method (no prior venesection at least 1 month). Statistical analysis involved descriptive statistics and chi-square test. Results There were 71 males and 4 females, mean age 46 y (range 17-75 y). Increased RCM was found in 41/75 (55%). Positive JAK2 V617F was found in 13/75 patients (17%), who also had RCM above the mean normal predicted value, however, when the WHO RCM criteria were applied, only 7/13 (54%) could be considered as having “truly” increased RCM. In the patient group with negative JAK2 V617F test, 12/28 (43%) had RCM results as per WHO criteria. There was no statistical association between presence of JAK2 V617F and the RCM values. Conclusion In patients with negative JAK2 V617F but with high clinical suspicion for PV and all other causes of secondary and idiopathic erythrocytosis excluded, an increase in RCM would support the diagnosis of PV (about 10 % PV cases). In patients with JAK2 positive mutation and high haematocrit but RCM below the WHO cut-off level, an increased RCM would still count to confirm the diagnosis as the current standard level seems too stringent. References James C, Ugo V, Le Couedic JP, Staerk J, Delhommeau F, Lacout C et al. A unique clonal JAK2 mutation leading to constitutive signaling causes polycythaemia vera. Nature 2005; 434(7037): 1144-8. Kralovics R, Passamonti F, Buser AS, Soon-Siong T, Tiedt R, Passweg JR, et al. A Gain-of-Function Mutation of JAK2 in Myeloproliferative Disorders. Merck Manual of Diagnosis and Therapy. 16th Edition, 1992 McMullin MF, Bareford D, Campbell P, Green AR, Claire Harrison C, Hunt B, Oscier D, et al. Guidelines for the diagnosis, investigation and management of polycythaemia/erythrocytosis. British Journal of Haematology 2005; 130(2): 174-95. Scott LM, Tong W, Levine RL, et al. JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis. N Engl J Med. 2007;356:459-468. Pardanani A, Lasho TL, Finke C, et al. Prevalence and clinicopathologic correlates of JAK2 exon 12 mutations in JAK2V617F-negative polycythemia vera. Leukemia. 2007;21:1960-1963. Pancrazzi A, Guglielmelli P, Ponziani V, et al. A sensitive detection method for MPLW515L or MPLW515K mutation in chronic myeloproliferative disorders with locked nucleic acid-modified probes and real-time polymerase chain reaction. J Mol Diagn. 2008;10:435-441. Disclosures: No relevant conflicts of interest to declare.


1999 ◽  
Vol 15 (3) ◽  
pp. 602-607 ◽  
Author(s):  
Lionel Pazart ◽  
Françoise Carpentier ◽  
Alain Durocher ◽  
Chrystelle Mougeot ◽  
Yves Najean ◽  
...  

Objective: To assess the impact of guidelines on drug use issued by a consensus conference on polycythemia vera held in Paris in June 1993. 32Phosphorus (32P) was recommended for patients over 70 and/or at risk, whereas pipobroman and hydroxyurea were recommended for patients under 70.Methods: A questionnaire was sent to all 119 departments of nuclear medicine in France 1 year after the conference to find out whether and how often they measured plasma volume and red cell mass (the recommended diagnostic tests for polycythemia vera). Time-series analyses were performed on sales of 32P, pipobroman (both virtually exclusively prescribed for polycythemia), and hydroxyurea over a 4-year span (January 1992–December 1995).Results: The average number of plasma volume determinations per year did not change significantly after the conference (22 ± 26 before vs 21 ± 25 after). 32P and pipobroman sales were stable until July 1993, when 32P sales decreased while pipobroman sales rose steadily. Hydroxyurea sales increased over the whole period with no change in trend after the guidelines were published.Conclusions: The guidelines apparently influenced clinical practice since sales of drugs that are specifically used to treat polycythemia vera showed clear changes in trend after publication of the guidelines. This type of study seems to be an effective way of assessing the impact of consensus conferences.


Blood ◽  
1979 ◽  
Vol 53 (6) ◽  
pp. 1076-1084 ◽  
Author(s):  
N Dainiak ◽  
R Hoffman ◽  
AI Lebowitz ◽  
L Solomon ◽  
L Maffei ◽  
...  

Abstract We investigated the pathogenesis of isolated erythrocytosis of 14 yr duration in a 28-yr-old man. The increase in red cell mass was attributed to increased erythropoietin production. An extensive search for recognized causes of secondary erythrocytosis was unrevealing. Family members were found to be hematologically normal. After reduction of the circulating red cell mass by 20%, erythropoietin activity nearly quadrupled, thus suggesting a normal erythropoietin response to phlebotomy. When bone marrow cells of the patient were cultured in plasma clots in the absence of added erythropoietin, endogenous erythroid colony formation was observed, a pattern previously believed to be specific for polycythemia vera bone marrow cells. Our observations suggest that the erythrocytosis in this individual is best explained by an abnormal “servoregulatory” mechanism of erythropoietin production. In addition, this is the first instance in which the rule that endogenous erythroid colony formation is correlated with the diagnosis of polycythemia vera has not held.


2018 ◽  
Vol 97 (9) ◽  
pp. 1581-1590 ◽  
Author(s):  
Ljubomir Jakovic ◽  
Mirjana Gotic ◽  
Heinz Gisslinger ◽  
Ivan Soldatovic ◽  
Dijana Sefer ◽  
...  

1977 ◽  
Vol 232 (1) ◽  
pp. H79-H84 ◽  
Author(s):  
J. I. Spector ◽  
C. G. Zaroulis ◽  
L. E. Pivacek ◽  
C. P. Emerson ◽  
C. R. Valeri

Baboons were bled one-third their red cell mass and were given homologous transfusions of red blood cells to restore the red cell volume. One group of baboons received red blood cells with a normal 2,3-diphosphoglycerate 2,3-DPG) level and normal affinity for oxygen, and in this group the 2,3-DPG level after transfusion was normal. The other group received red blood cells with a 160% of normal 2,3-DPG level and decreased affinity for oxygen, and in this group the 2,3-DPG level after transfusion was 125% of normal. In both groups of baboons, the inspired oxygen concentration was lowered and arterial PO2 tension was maintained at 55-60 mmHg for 2 h after transfusion. During the hypoxic state, systemic oxygen extraction was similar in the two groups, whereas oxygen saturation was lower in the high 2,3-DPG group than in the control animals. Cardiac output was significantly reduced 30 min after the arterial PO2 was restored to normal. These data indicate that red blood cells with decreased affinity for oxygen maintained satisfactory oxygen delivery to tissue during hypoxia.


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