Occlusive Arterial Disease and Blood Rheology

Lowe, G. D. O.; Forbes, C. D.; Barbenel, J.C.

doi:10.1007/978-1-4471-3105-2_13

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Primary Hyperviscosity Condition1

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2017

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Cited by 12 publications

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“…Primary hyperviscosity condition may be subdivided into polycythemic, plasma and sclerocythemic [8,21,26,58,59].…”

Section: Primary Hyperviscosity Conditionmentioning

confidence: 99%

Clinical conditions responsible for hyperviscosity and skin ulcers complications

Caimi

Canino

Presti

et al. 2017

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Abstract.In this brief review, we have examined some clinical conditions that result to be associated to an altered hemorhe-6 ological profile and at times accompanied by skin ulcers. This skin condition may be observed in patients with the following 7 condtions, such as primary polycythemic hyperviscosity (polycythemia, thrombocytemia) treated with hydroxyurea, primary 8 plasma hyperviscosity (multiple myeloma, cryoglobulinemia, cryofibrinogenemia, dysfibrinogenemia, and connective tissue 9 diseases), primary sclerocythemic hyperviscosity (hereditary spherocytosis, thalassemia, and sickle cell disease). In addition, 10it may be present in patients with secondary hyperviscosity conditions such as diabetes mellitus, arterial hypertension, critical 11 limb ischemia and chronic venous insufficiency.

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“…Primary hyperviscosity condition may be subdivided into polycythemic, plasma and sclerocythemic [8,21,26,58,59].…”

Section: Primary Hyperviscosity Conditionmentioning

confidence: 99%