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Department

About the department

Department name (English): Clinical Haematology

Department name (original): Hematologia Clínica

Subnetworks of expertise:

  • Myeloid malignancies
  • Lymphoid malignancies
  • Bleeding - Coagulation disorders
  • Hemochromatosis and other iron disorders

Healthcare provider: Centro Hospitalar do Porto, EPE

Diseases covered by the department:

  • Tumor of hematopoietic and lymphoid tissues
  • Mastocytosis
  • Systemic mastocytosis
  • Indolent systemic mastocytosis
  • Smouldering systemic mastocytosis
  • Isolated bone marrow mastocytosis
  • Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
  • Aggressive systemic mastocytosis
  • Lymphoadenopathic mastocytosis with eosinophilia
  • Mast cell leukemia
  • Classic mast cell leukemia
  • Aleukemic mast cell leukemia
  • Cutaneous mastocytosis
  • Cutaneous mastocytoma
  • Diffuse cutaneous mastocytosis
  • Bullous diffuse cutaneous mastocytosis
  • Pseudoxanthomatous diffuse cutaneous mastocytosis
  • Maculopapular cutaneous mastocytosis
  • Telangiectasia macularis eruptiva perstans
  • Typical urticaria pigmentosa
  • Plaque-form urticaria pigmentosa
  • Nodular urticaria pigmentosa
  • Mast cell sarcoma
  • Extracutaneous mastocytoma
  • Essential thrombocythemia
  • Hereditary thrombocytopenia with early-onset myelofibrosis
  • Gaisböck syndrome
  • Rare coagulation disorder
  • Rare thrombotic disease of hematologic origin
  • Rare thrombotic disorder due to a coagulation factors defect
  • Rare thrombotic disorder due to a constitutional coagulation factors defect
  • Congenital factor XII deficiency
  • Familial thrombomodulin anomalies
  • Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
  • Rare hereditary thrombophilia
  • Hereditary thrombophilia due to congenital protein S deficiency
  • Hereditary thrombophilia due to congenital protein C deficiency
  • Hereditary thrombophilia due to congenital antithrombin deficiency
  • Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
  • Rare thrombotic disorder due to an acquired coagulation factors defect
  • Catastrophic antiphospholipid syndrome
  • Heparin-induced thrombocytopenia
  • Protein S acquired deficiency
  • Acquired purpura fulminans
  • Simple cryoglobulinemia
  • Rare thrombotic disorder due to a platelet anomaly
  • Thrombotic thrombocytopenic purpura
  • Congenital thrombotic thrombocytopenic purpura
  • Acquired thrombotic thrombocytopenic purpura
  • Rare thrombotic disorder due to a constitutional platelet anomaly
  • Familial thrombocytosis
  • Hereditary thrombocytosis with transverse limb defect
  • Rare thrombotic disorder due to an acquired platelet anomaly
  • Rare hemorrhagic disorder
  • Rare hemorrhagic disorder due to a coagulation factors defect
  • Rare hemorrhagic disorder due to a constitutional coagulation factors defect
  • Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
  • Hemophilia
  • Hemophilia A
  • Severe hemophilia A
  • Moderately severe hemophilia A
  • Mild hemophilia A
  • Symptomatic form of hemophilia A in female carriers
  • Hemophilia B
  • Severe hemophilia B
  • Moderately severe hemophilia B
  • Mild hemophilia B
  • Symptomatic form of hemophilia B in female carriers
  • Congenital factor V deficiency
  • Congenital fibrinogen deficiency
  • Familial afibrinogenemia
  • Familial dysfibrinogenemia
  • Familial hypofibrinogenemia
  • Familial hypodysfibrinogenemia
  • Congenital alpha2-antiplasmin deficiency
  • Congenital factor XIII deficiency
  • Von Willebrand disease
  • Von Willebrand disease type 1
  • Von Willebrand disease type 2
  • Von Willebrand disease type 2A
  • Von Willebrand disease type 2B
  • Von Willebrand disease type 2M
  • Von Willebrand disease type 2N
  • Von Willebrand disease type 3
  • Congenital factor XI deficiency
  • Congenital plasminogen activator inhibitor type 1 deficiency
  • Congenital high-molecular-weight kininogen deficiency
  • Congenital prekallikrein deficiency
  • Combined deficiency of factor V and factor VIII
  • Congenital vitamin K-dependent coagulation factors deficiency
  • Congenital factor VII deficiency
  • Congenital factor II deficiency
  • Congenital factor X deficiency
  • Hereditary combined deficiency of vitamin K-dependent clotting factors
  • Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
  • East Texas bleeding disorder
  • Thrombomodulin-related bleeding disorder
  • Rare hemorrhagic disorder due to an acquired coagulation factor defect
  • Acquired prothrombin deficiency
  • Acquired hemophilia
  • Acquired von Willebrand syndrome
  • Rare hemorrhagic disorder due to a platelet anomaly
  • Rare hemorrhagic disorder due to a constitutional platelet anomaly
  • Rare hemorrhagic disorder due to a constitutional thrombocytopenia
  • Syndromic constitutional thrombocytopenia
  • Stormorken-Sjaastad-Langslet syndrome
  • Thrombocytopenia-absent radius syndrome
  • Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome
  • MYH9-related disease
  • GNE myopathy
  • Jacobsen syndrome
  • Macrothrombocytopenia with mitral valve insufficiency
  • Alpha delta granule deficiency
  • Dense granule disease
  • Wiskott-Aldrich syndrome
  • Chédiak-Higashi syndrome
  • Hereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndrome
  • Hermansky-Pudlak syndrome
  • Hermansky-Pudlak syndrome with neutropenia
  • Hermansky-Pudlak syndrome with pulmonary fibrosis
  • Hermansky-Pudlak syndrome without pulmonary fibrosis
  • Hermansky-Pudlak syndrome type 7
  • Hermansky-Pudlak syndrome type 8
  • Hermansky-Pudlak syndrome type 9
  • Isolated constitutional thrombocytopenia
  • Isolated hereditary giant platelet disorder
  • Severe autosomal recessive macrothrombocytopenia
  • Bernard-Soulier syndrome
  • Thrombocytopenia with congenital dyserythropoietic anemia
  • Autosomal dominant macrothrombocytopenia
  • Alpha granule disease
  • Gray platelet syndrome
  • Quebec platelet disorder
  • Medich giant platelet syndrome
  • White platelet syndrome
  • Paris-Trousseau thrombocytopenia
  • X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
  • Hereditary thrombocytopenia with normal platelets
  • X-linked thrombocytopenia with normal platelets
  • Autosomal thrombocytopenia with normal platelets
  • Congenital amegakaryocytic thrombocytopenia
  • Bleeding diathesis due to thromboxane synthesis deficiency
  • Isolated delta-storage pool disease
  • Autosomal dominant thrombocytopenia with platelet secretion defect
  • Rare hemorrhagic disorder due to a qualitative platelet defect
  • Glanzmann thrombasthenia
  • Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
  • Ehlers-Danlos syndrome, fibronectinemic type
  • Scott syndrome
  • P2Y12 defect
  • Pseudo-von Willebrand disease
  • Bleeding diathesis due to a collagen receptor defect
  • Bleeding diathesis due to glycoprotein VI deficiency
  • Bleeding diathesis due to integrin alpha2-beta1 deficiency
  • Bleeding disorder due to CalDAG-GEFI deficiency
  • Rare hemorrhagic disorder due to an acquired platelet anomaly
  • Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome
  • TAFRO syndrome
  • HELLP syndrome
  • Fetal and neonatal alloimmune thrombocytopenia
  • Autoimmune thrombocytopenia
  • Immune thrombocytopenic purpura
  • Evans syndrome
  • STAT3-related early-onset multisystem autoimmune disease
  • Kasabach-Merritt syndrome
  • Rare anemia
  • Rare deficiency anemia
  • Rare hereditary hemochromatosis
  • HFE related hereditary hemochromatosis (Symptomatic form of hemochromatosis type 1) - OMIM 235200
  • HJV related hereditary hemochromatosis - OMIM 602390 (Hemochromatosis type 2A)
  • HAMP related hereditary hemochromatosis - OMIM 613313 (Hemochromatosis type 2B)
  • TFR2 related hereditary hemochromatosis OMIM 604250 (Hemochromatosis type 3)
  • FTH related hereditary hemochromatosis - OMIM 615517 (Hemochromatosis type 5)
  • Ferroportin Disease (Hemochromatosis type 4B)​
  • SLC40A1 related hereditary hemochromatosis - OMIM 606069 (Hemochromatosis type 4A)
  • Rare iron overload
  • Rare Ferritinopathy

Service offered

  • Prevention and genetic counseling
  • Diagnostics
  • Treatment and care

Patients covered

  • Pediatrics
  • Adults
  • Ageing

Health professionals

Name Surname Academic title Charge