Chapter 28 The Polycythemias Marina Kremyanskaya, Vesna Najfeld, John Mascarenhas, Ronald Hoffman Table 28-1 Differential Diagnosis of the Polycythemias Relative or Spurious Polycythemia 1. Decreased plasma volume—reduced fluid intake, marked loss of body fluids (diaphoresis, vomiting, diarrhea, “third spacing”) 2. Gaisböck syndrome 3. Overfilling of blood in collection vacuum tubes Absolute Polycythemia 1. Secondary polycythemia A. Acquired Hypoxia • Pulmonary disease • Cyanotic congenital heart disease • Hypoventilation syndromes: sleep apnea, Pickwickian syndrome • High altitude • Smokers’ polycythemia, hookah polycythemia, carbon monoxide intoxication caused by industrial exposure Postrenal transplantation erythrocytosis Aberrant erythropoietin production • Tumors: renal cell carcinoma, Wilms tumor, hepatic carcinoma, uterine leiomyomata, virilizing ovarian tumors, vascular cerebellar tumors • Miscellaneous renal and hepatic disorders: solitary renal cysts, polycystic kidney disease, renal artery stenosis hydronephrosis, viral hepatitis Endocrine disorders: Cushing syndrome, primary aldosteronism Androgen use Erythropoietin use B. Congenital Polycythemias • Abnormal high-affinity hemoglobin variants • Bisphosphoglycerate deficiency • Congenital methemoglobinemia • Chuvash polycythemia (von Hippel Lindau mutations) • Prolyl hydroxylase mutations • Hypoxia-inducible factor gene mutations 2. Primary polycythemias • Primary congenital and familial polycythemia • Polycythemia vera Figure 28-1 EVOLUTION OF POLYCYTHEMIA VERA (PV). MF, Myelofibrosis. Table 28-2 International Working Group for Myelofibrosis Research and Recommended Treatment Criteria for Post-PV MF Required Criteria: 1. Documentation of a previous diagnosis of polycythemia vera as defined by the WHO criteria 2. Bone marrow fibrosis grade 2-3 (on 0-3 scale) or grade 3-4 (on 0-4 scale) Additional Criteria (Two Are Required): Only gold members can continue reading. Log In or Register to continue Share this:Click to share on Twitter (Opens in new window)Click to share on Facebook (Opens in new window) Related Related posts: Diagnosis and Treatment of Diffuse Large B-Cell Lymphoma and Burkitt Lymphoma Hematologic Manifestations of Cancer Acquired Disorders of Red Cell, White Cell, and Platelet Production Hematology in Aging Disorders of Phagocyte Function Inherited Forms of Bone Marrow Failure Stay updated, free articles. Join our Telegram channel Join Tags: Hematology Diagnosis and Treatment Jun 12, 2016 | Posted by admin in HEMATOLOGY | Comments Off on The Polycythemias Full access? Get Clinical Tree Get Clinical Tree app for offline access Get Clinical Tree app for offline access
Chapter 28 The Polycythemias Marina Kremyanskaya, Vesna Najfeld, John Mascarenhas, Ronald Hoffman Table 28-1 Differential Diagnosis of the Polycythemias Relative or Spurious Polycythemia 1. Decreased plasma volume—reduced fluid intake, marked loss of body fluids (diaphoresis, vomiting, diarrhea, “third spacing”) 2. Gaisböck syndrome 3. Overfilling of blood in collection vacuum tubes Absolute Polycythemia 1. Secondary polycythemia A. Acquired Hypoxia • Pulmonary disease • Cyanotic congenital heart disease • Hypoventilation syndromes: sleep apnea, Pickwickian syndrome • High altitude • Smokers’ polycythemia, hookah polycythemia, carbon monoxide intoxication caused by industrial exposure Postrenal transplantation erythrocytosis Aberrant erythropoietin production • Tumors: renal cell carcinoma, Wilms tumor, hepatic carcinoma, uterine leiomyomata, virilizing ovarian tumors, vascular cerebellar tumors • Miscellaneous renal and hepatic disorders: solitary renal cysts, polycystic kidney disease, renal artery stenosis hydronephrosis, viral hepatitis Endocrine disorders: Cushing syndrome, primary aldosteronism Androgen use Erythropoietin use B. Congenital Polycythemias • Abnormal high-affinity hemoglobin variants • Bisphosphoglycerate deficiency • Congenital methemoglobinemia • Chuvash polycythemia (von Hippel Lindau mutations) • Prolyl hydroxylase mutations • Hypoxia-inducible factor gene mutations 2. Primary polycythemias • Primary congenital and familial polycythemia • Polycythemia vera Figure 28-1 EVOLUTION OF POLYCYTHEMIA VERA (PV). MF, Myelofibrosis. Table 28-2 International Working Group for Myelofibrosis Research and Recommended Treatment Criteria for Post-PV MF Required Criteria: 1. Documentation of a previous diagnosis of polycythemia vera as defined by the WHO criteria 2. Bone marrow fibrosis grade 2-3 (on 0-3 scale) or grade 3-4 (on 0-4 scale) Additional Criteria (Two Are Required): Only gold members can continue reading. Log In or Register to continue Share this:Click to share on Twitter (Opens in new window)Click to share on Facebook (Opens in new window) Related Related posts: Diagnosis and Treatment of Diffuse Large B-Cell Lymphoma and Burkitt Lymphoma Hematologic Manifestations of Cancer Acquired Disorders of Red Cell, White Cell, and Platelet Production Hematology in Aging Disorders of Phagocyte Function Inherited Forms of Bone Marrow Failure Stay updated, free articles. Join our Telegram channel Join Tags: Hematology Diagnosis and Treatment Jun 12, 2016 | Posted by admin in HEMATOLOGY | Comments Off on The Polycythemias Full access? Get Clinical Tree Get Clinical Tree app for offline access Get Clinical Tree app for offline access