Pedro Rafael Camacho Maldonado, MD

As a Classical Hematologist, my philosophy is to provide the best possible care for my patients, understanding them as a whole person, and taking advantage of the most up to date treatments available.

Keywords therapeutic phlebotomy, severe neutropenia, severe thrombocytopenia, severe anemia, hypereosinophilic syndrome, complement mediated hemolytic uremic syndrome, decreased hemoglobin, iron replacement, iron level, iron binding capacity, ferritin, cardiolipin antibody assay, thalassemia trait, family history of clotting, hypersplenism, hemophilia carrier, family history of bleeding, acquired factor inhibitor, nucleated red blood cell count, monoclonal paraproteinemia, giant platelet syndrome, prolonged partial thromboplastin time, prolonged prothrombin time, plasminogen disorder, monoclonal b-cell lymphocytosis, microcytosis, macrocytosis, factor i deficiency, elevated hemoglobin, high iron, autoimmune (aa) amyloidosis, light chain (al) amyloidosis, thrombotic microangiopathy, paraprotein associated cryoglobulinemia, abnormal protein, spherocytosis, iron infusion therapy, pyruvate kinase deficiency (pkd), acquired sideroblastic anemia, congenital sideroblastic anemia (csa), vaccine induced prothrombotic immune thrombocytopenia, gestational thrombocytopenia, mesenteric vein thrombosis, cervical lymphadenopathy, axillary lymphadenopathy, partial thromboplastin time blood test, leukocytosis, anemia and bone marrow disorders, white blood cell disorders, red blood cell disorders, protein s deficiency, protein c deficiency, plasma cell and antibody production disorders, iron metabolism disorders, essential thrombocytosis, cold agglutinin disease, autoimmune hemolytic anemia, splenic sequestration, porphyria, cryoglobulinemia, thrombotic disorders, recurrent thrombosis, prothrombin gene mutation, post thrombotic syndrome (pts), monoclonal gammopathy of undetermined significance, langerhans cell histiocytosis, shwachman diamond syndrome, chronic granulomatous disorder, venous occlusive crisis, severe congenital neutropenia, rh incompatibility, reticular dysgenesis, purpura, paroxysmal nocturnal hemoglobinuria, maternal thrombophilia, maternal anticoagulation, lupus anticoagulant, light chain disorders, hypogammaglobulinemia, histiocytosis, hereditary spherocytosis, hemochromatosis, folic acid deficiency, dyskeratosis congenita, deep vein thrombosis, deep thrombophlebitis, catastrophic antiphospholipid syndrome (caps), platelet disorder, blood clot, antiphospholipid syndrome, anticoagulation, lymphedema physical therapy, chemotherapy iv infusion, rectal neuroendocrine tumor, neuroendocrine carcinoma, metastatic neuroendocrine tumors, relapsed myeloma, colon adenocarcinoma, adjuvant chemotherapy, neutrophilia.