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Thrombocytosis

Thrombocytosis is the presence of high platelet counts in the blood, and can be either reactive or primary (also termed essential and caused by a myeloproliferative disease). Although often symptomless (particularly when it is a secondary reaction), it can predispose to thrombosis in some patients. more...

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Generally, a normal platelet count ranges from 150,000 and 450,000 per mm3. These limits, however, are determined by the 2.5th lower and upper percentile, and a deviation does not necessary imply any form of disease. Nevertheless, counts over 750,000 (and especially over a million) are considered serious enough to warrant investigation and intervention.

Signs and symptoms

High platelet levels do not necessarily signal any clinical problems, and are picked up on a routine full blood count. However, it is important that a full medical history be elicited to ensure that the increased platelet count is not due to a secondary process. Often, it occurs in tandem with an inflammatory disease, as the principal stimulants of platelet production (e.g. thrombopoietin) are elevated in these clinical states as part of the acute phase reaction.

High platelet counts can occur in patients with polycythemia vera (high red blood cell counts), and is an additional risk factor for complications.

A very small segment of patients report symptoms of erythromelalgia, a burning sensation and redness of the extremities that resolves with cooling and/or aspirin use.

Diagnosis

Laboratory tests might include: full blood count, liver enzymes, renal function and erythrocyte sedimentation rate.

If the cause for the high platelet count remains unclear, bone marrow biopsy is often undertaken, to differentiate whether the high platelet count is reactive or essential.

Causes

Increase platelet counts can be due to a number of disease processes:

  • Essential (primary)
    • Essential thrombocytosis (a form of myeloproliferative disease)
    • Other myeloproliferative disorders such as chronic myelogenous leukemia, polycythemia vera, myelofibrosis
  • Reactive (secondary)
    • Inflammation
    • Surgery (which leads to an inflammatory state)
    • Hyposplenism (decreased breakdown due to decreased function of the spleen)
    • Iron deficiency

Treatment

Often, no treatment is required or necessary for reactive thrombocytosis.

However, in primary thrombocytosis, if platelet counts are over 750,000 or 1,000,000, and especially if there are other risk factors for thrombosis. Aspirin at low doses is thought to be protective, and extreme levels are treated with hydroxyurea (a cytoreducing agent). The new agent anagrelide (Agrylin®) has recently been introduced for the treatment of essential thrombocytosis. However, recent studies show that anegrilide is not significantly more effective than traditionally used hydroxyurea (Harrison et al 2005).

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PERIPHERAL BLOOD FINDINGS IN INFILTRATIVE MYELOPATHY BY PARACOCCIDIOIDOMYCOSIS. EVALUATION OF 19 PATIENTS, A SYSTEMATIC REVIEW AND META-ANALYSIS
From Revista do Instituto de Medicina Tropical de Sao Paulo, 10/1/05 by Resende, L S R

Resende, L. S. R.1; Mendes, R. P.2; Bacchi, M. M.3; Marques, S. A.4; Barraviera, B.5; Souza, L. R.6; Meira, D. A.7; Niero-Melo, L.8

1,8 Faculdade de Medicina de Botucatu/UNESP - Serviço de Hematologia da Clínica Médica; 2,5,6,7 Faculdade de Medicina de Botucatu/UNESP - Doenças Tropicais e Diagnóstico por Imagem; 3 Faculdade de Medicina de Botucatu/UNESP - Patologia; 4 Faculdade de Medicina de Botucatu Dermatologia e Radioterapia

Introduction and Objectives: In primary or secondary bone marrow involvement from any disease, peripheral blood (PB) can reveal "clues" that indicate a cyto-histological study of this tissue. The aim of this study is to analyse PB parameters of paracoccidioidomycosis (PCM) patients that can suggest infiltrative myelopathy. Methods and Results: It was achieved a retrospective evaluation of PB data from 19 PCM patients, whose bone marrow involvement was diagnosed in life or necropsy, at the Botucatu University Hospital. Literature review was performed identifying 20 additional cases. Isolated or combined cytopenias (except isolated monocytopenias or anemias) and leucoerythroblnstic reaction (LER) were considered indicative findings for bone marrow study. The main findings were: anemia (35/37; 94.6%), normal hemoglobin value (2/37; 5.4%); leucopenia (2/38; 5.3%), leucocytosis (16/38; 42.1%), normal leucocyte count (20/38; 52.6%); neutropenia (2/30; 6.7%), neutrophilia (13/30; 43.3%), normal neutrophil count (15/30; 50.0%); eosinophilia (21/34; 61,8%), normal eosinophil count (13/34; 38.2%); basophilia (5/30; 16.7%), normal basophil count (25/30; 83.3%); lymphopenia (9/31; 29.0%), lymphocitosis (2/31; 6.5%), normal lymphocyte count (20/31; 64.5%); monocytopenia (7/30; 23.3%), monocytosis (12/30; 40.0%), normal monocyte count (11/30; 36.7%); thrombocytopenia (22.2%), thrombocytosis (27.8%), normal trombocyte count (50.0%). Granulocytic left shift was verified in (28/32; 87,5%). Six patients showed simultaneous erythroid left shift, characterizing LER, with or without cytopenias. Eight presented with cytopenias, characterized as lymphocytopenia in 6, lymphocytopenia plus thrombocytopenia in 1, and pancytopenia in 1. Conclusions: The PB parameters varied from normal to markedly altered values in one or more hematological lineages. Only 14/39 patients (35.9%) were indicated for bone marrow examination in this study exclusively by abnormal peripheral blood parameters. Other indications should be assessed by suitable clinical and laboratory evaluation in each case, as in those with suspected simultaneous hematological neoplasia or with unsatisfactory response to treatment. References: Resende LSR, Mendes RP, Bacchi MM et al. Infiltrative myelopathy by paracoccidioidomycosis. Histopathol: 2005 (in press).

Copyright Instituto de Medicina Tropical de Sao Paulo Oct 2005
Provided by ProQuest Information and Learning Company. All rights Reserved

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