SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Pädiatrie 5 – Onkologie, Hämatologie und Immunologie am Klinikum Stuttgart

Description of facility

Director / Spokesperson
PD Dr. Claudia Blattmann
Information
Care facility for children
Description
Die Klinik betreut Kinder und Jugendliche mit Erkrankungen aus den Bereichen Onkologie, Hämatologie und Immunologie nach neuesten Erkenntnissen. Als kinderonkologisches Zentrum der Region Stuttgart und eine der größten Spezialabteilungen bundesweit ist die Klinik Anlaufstelle bei allen Krebserkrankungen junger Menschen, bei Erkrankungen des Blutes und der Immunabwehr.

Ein besonderer Schwerpunkt liegt auf der Versorgung junger Menschen mit Sarkomen, also Krebserkrankungen des Binde- oder Stützgewebes. Die Pädiatrie 5 – Onkologie, Hämatologie und Immunologie ist Sitz der Studienzentralen der Osteo- und Weichteilsarkomgruppen (COSS & CWS) der nationalen Fachgesellschaft, der Gesellschaft für Pädiatrische Onkologie und Hämatologie GPOH. Neben der damit verbundenen Funktion als Referenz- und Konsiliarzentrum koordiniert das Klinikum deutschlandweit und darüber hinaus die Erforschung und Behandlung dieser seltenen Krebserkrankungen, führt zahlreiche wissenschaftliche Projekte und Studien zu Knochen- und Weichteilkrebs durch und beteiligt sich an Therapieoptimierungsstudien zu anderen Krebsarten.

Consultation hours

nach Vereinbarung.

Care provisions

This facility offers the following
  • Clinical studies / research
  • Diagnostic
  • Therapy

Contact

Sekretariat Feven Assefaw
0711 27872461
0711 27872462
f.assefaw@klinikum-stuttgart.de
Website http://www.klinikum-stuttgart.de/kliniken-institute-zentren/paediatrie-5-onkologie-haematologie-und-immunologie/startseite/

Address

Kriegsbergstraße 62
70174 Stuttgart

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Certificates 2

European Reference Network 1

Preview of the assigned diseases 2

Extraskeletal Ewing sarcoma Intraneural perineurioma Painful orbital and systemic neurofibromas-marfanoid habitus syndrome Angiocentric glioma Alpha-thalassemia Extraneural perineurioma Alveolar soft tissue sarcoma Sclerosing perineurioma Ependymal tumor Mycosis fungoides and variants Hereditary folate malabsorption Spermatocytic seminoma Aregenerative anemia Primary cutaneous B-cell lymphoma Simple cryoglobulinemia Alpha-thalassemia-X-linked intellectual disability syndrome Beta-thalassemia Secondary hypereosinophilic syndrome Bleeding diathesis due to a collagen receptor defect Hereditary orotic aciduria Glanzmann thrombasthenia Hemoglobinopathy Acquired hemophilia Ganglioglioma Lymphoadenopathic mastocytosis with eosinophilia May-Hegglin thrombocytopenia OSLAM syndrome Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Microcytic anemia with liver iron overload Paris-Trousseau thrombocytopenia Primary bone lymphoma Rare thrombotic disorder due to a constitutional platelet anomaly Chordoid glioma X-linked thrombocytopenia with normal platelets Primary intraocular lymphoma Dysembryoplastic neuroepithelial tumor Beta-thalassemia major Fetal and neonatal alloimmune thrombocytopenia Beta-thalassemia intermedia Primary central nervous system lymphoma Hereditary thrombocytopenia with normal platelets Astroblastoma Thyroid lymphoma Paroxysmal nocturnal hemoglobinuria Methylmalonic acidemia with homocystinuria, type cblC Rare thrombotic disorder due to an acquired platelet anomaly Bleeding diathesis due to thromboxane synthesis deficiency Craniopharyngioma Constitutional dyserythropoietic anemia Combined deficiency of factor V and factor VIII Classic mast cell leukemia Hemophilia Myeloid hemopathy Methylmalonic acidemia with homocystinuria type cblF Meningioma Dominant beta-thalassemia Anaplastic ganglioglioma Hepatoblastoma Inherited acute myeloid leukemia Optic pathway glioma Myelodysplastic syndrome Malignant non-dysgerminomatous germ cell tumor of ovary Primary organ-specific lymphoma POEMS syndrome Transcobalamin deficiency Angiosarcoma Methylmalonic acidemia with homocystinuria, type cblD Aleukemic mast cell leukemia Congenital dyserythropoietic anemia type IV Familial hypodysfibrinogenemia Macrothrombocytopenia with mitral valve insufficiency Thiamine-responsive megaloblastic anemia syndrome Papillary glioneuronal tumor Beta-thalassemia associated with another hemoglobin anomaly Refractory anemia with excess blasts type 2 Refractory anemia with excess blasts type 1 Essential thrombocythemia Rare hereditary thrombophilia Embryonal carcinoma of the central nervous system Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16 Acute erythroid leukemia Congenital amegakaryocytic thrombocytopenia Extramedullary soft tissue plasmacytoma Thrombotic thrombocytopenic purpura Bone sarcoma Skeletal Ewing sarcoma Lymphoid hemopathy Thrombocytopenia-absent radius syndrome Isolated hereditary giant platelet disorder Acute myeloid leukemia with CEBPA somatic mutations Primary plasmacytoma of the bone Extragonadal germinoma Polycythemia vera Mu-heavy chain disease Esthesioneuroblastoma Multiple osteochondromas Hoyeraal-Hreidarsson syndrome Evans syndrome Hemoglobin H disease Primary systemic amyloidosis Rare constitutional aplastic anemia Familial thrombomodulin anomalies Primary cutaneous T-cell lymphoma Gamma-heavy chain disease Epignathus Alpha-heavy chain disease Peripheral primitive neuroectodermal tumor Autosomal thrombocytopenia with normal platelets Heparin-induced thrombocytopenia Congenital factor II deficiency High-grade astrocytoma Alpha delta granule deficiency Post-transplant lymphoproliferative disease Congenital factor V deficiency Lymphoma Hemoglobinopathy Toms River Congenital factor VII deficiency Desmoid tumor Delta-beta-thalassemia Embryonal rhabdomyosarcoma Congenital factor X deficiency Acquired purpura fulminans Rare tumor of neuroepithelial tissue Alveolar rhabdomyosarcoma Embryonal carcinoma Congenital plasminogen activator inhibitor type 1 deficiency Congenital factor XI deficiency WT limb-blood syndrome Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder Congenital factor XII deficiency Yolk sac tumor Hemoglobin C-beta-thalassemia syndrome Congenital factor XIII deficiency Congenital intrinsic factor deficiency Polyembryoma Primary localized amyloidosis Formiminoglutamic aciduria Severe hereditary thrombophilia due to congenital protein S deficiency AL amyloidosis Constitutional deficiency anemia Hb Bart's hydrops fetalis Congenital fibrinogen deficiency Mixed germ cell tumor Liposarcoma Severe hereditary thrombophilia due to congenital protein C deficiency Rare deficiency anemia B-cell non-Hodgkin lymphoma Rare acquired aplastic anemia Epstein syndrome Rhabdoid tumor Rhabdoid tumor predisposition syndrome Rosette-forming glioneuronal tumor Extragonadal teratoma Hypoxanthine-guanine phosphoribosyltransferase deficiency Methylmalonic acidemia with homocystinuria, type cblJ Hemoglobin E-beta-thalassemia syndrome Congenital prekallikrein deficiency Stormorken-Sjaastad-Langslet syndrome Autosomal dominant macrothrombocytopenia Beta-thalassemia with other manifestations T-cell non-Hodgkin lymphoma Bleeding disorder in hemophilia A carriers Leiomyosarcoma Constitutional megaloblastic anemia due to folate metabolism disorder Medulloblastoma Autosomal recessive sideroblastic anemia Non-central nervous system-localized embryonal carcinoma Rare acquired deficiency anemia Myeloproliferative neoplasm Pancreatic insufficiency-anemia-hyperostosis syndrome Malignant germ cell tumor of ovary Malignant peripheral nerve sheath tumor with perineurial differentiation Congenital high-molecular-weight kininogen deficiency Anaplastic/large cell medulloblastoma Extragonadal non-dysgerminomatous germ cell tumor Bleeding disorder due to P2Y12 defect Rare hemorrhagic disorder X-linked sideroblastic anemia and spinocerebellar ataxia Primary non-gestational choriocarcinoma of ovary Methylmalonic acidemia with homocystinuria, type cblX Fechtner syndrome Thrombocythemia with distal limb defects Lipoblastoma Osteoblastoma Myelodysplastic/myeloproliferative disease Diaphyseal medullary stenosis-bone malignancy syndrome Ovarian dysgerminoma Vitamin B12- and folate-independent constitutional megaloblastic anemia Hereditary methemoglobinemia Diffuse cutaneous mastocytosis IRIDA syndrome Maculopapular cutaneous mastocytosis Kaposiform hemangioendothelioma Atypical chronic myeloid leukemia Homocystinuria without methylmalonic aciduria Bleeding disorder in hemophilia B carriers Beta-thalassemia-X-linked thrombocytopenia syndrome Cutaneous mastocytoma Embryonal tumor of neuroepithelial tissue Glomus tumor Acute myeloid leukemia with recurrent genetic anomaly Thrombocytopenia with congenital dyserythropoietic anemia Chronic myelomonocytic leukemia Rare bone tumor Alpha-thalassemia-myelodysplastic syndrome Rare hemorrhagic disorder due to a constitutional thrombocytopenia Refractory anemia Adult-onset autosomal recessive sideroblastic anemia Primary germ cell tumor of central nervous system Papilloma of choroid plexus Congenital alpha2-antiplasmin deficiency Benign peripheral nerve sheath tumor Unclassified myelodysplastic/myeloproliferative disease Medulloblastoma with extensive nodularity Solitary fibrous tumor Nasopharyngeal teratoma Giant cell tumor of bone Plasma cell tumor Inflammatory myofibroblastic tumor Unclassified myelodysplastic syndrome Ganglioneuroma Acute myeloid leukemia with 11q23 abnormalities Hereditary thrombophilia due to congenital antithrombin deficiency Primary acquired red cell aplasia Desmoplastic/nodular medulloblastoma Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent Fanconi anemia Chronic myeloproliferative disease, unclassifiable Acute myeloblastic leukemia without maturation Rare hemorrhagic disorder due to a coagulation factors defect Histiocytic and dendritic cell tumor Von Willebrand disease Congenital dyserythropoietic anemia Chronic neutrophilic leukemia Acute myeloid leukemia with minimal differentiation Neuroepithelioma Gestational choriocarcinoma Hemoglobin C disease Acute undifferentiated leukemia Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor Cutaneous mastocytosis Dendritic cell tumor Hemoglobin E disease Von Willebrand disease type 1 Acute myeloblastic leukemia with maturation Revesz syndrome Classic medulloblastoma Unclassified acute myeloid leukemia Bullous diffuse cutaneous mastocytosis Macrophage or histiocytic tumor Acute biphenotypic leukemia Idiopathic aplastic anemia Juvenile myelomonocytic leukemia Lymphoproliferative disease associated with primary immune disease Nasal ganglioglioma Lhermitte-Duclos disease Deafness-lymphedema-leukemia syndrome Bilineal acute leukemia Chronic eosinophilic leukemia Low-grade astrocytoma Neuroblastoma Pleomorphic rhabdomyosarcoma Immunodeficiency-associated lymphoproliferative disease Von Willebrand disease type 2 Rare hemorrhagic disorder due to a platelet anomaly Hodgkin lymphoma Constitutional megaloblastic anemia with severe neurologic disease Rare coagulation disorder Melanoma of soft tissue Rare aplastic anemia Refractory cytopenia with multilineage dysplasia Mastocytosis Sideroblastic anemia Central nervous system embryonal tumor Refractory anemia with excess blasts Yolk sac tumor of central nervous system Myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2 Rare hemorrhagic disorder due to a qualitative platelet defect Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Astrocytoma Mediterranean macrothrombocytopenia Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality Hereditary combined deficiency of vitamin K-dependent clotting factors Sickle cell anemia Chondrosarcoma Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement Gonadal germ cell tumor Telangiectasia macularis eruptiva perstans Pseudoxanthomatous diffuse cutaneous mastocytosis Hemoglobin Lepore-beta-thalassemia syndrome Severe congenital hypochromic anemia with ringed sideroblasts Adamantinoma Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement Acute panmyelosis with myelofibrosis Beta-thalassemia and related diseases Rhabdomyosarcoma Primary lymphoma of the conjunctiva Von Willebrand disease type 2A Acute myeloid leukaemia with myelodysplasia-related features Indolent systemic mastocytosis Acute myeloid leukemia and myelodysplastic syndromes related to radiation Von Willebrand disease type 2M Maffucci syndrome Extragonadal germ cell tumor Growing teratoma syndrome Ependymoblastoma Mast cell sarcoma Lesch-Nyhan syndrome Aggressive systemic mastocytosis Choriocarcinoma of the central nervous system Von Willebrand disease type 2B Primary pulmonary lymphoma Epithelioid sarcoma Therapy related acute myeloid leukemia and myelodysplastic syndrome Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement Systemic mastocytosis with associated hematologic neoplasm Alpha-thalassemia and related disorders Ganglioneuroblastoma Acute basophilic leukemia Congenital atransferrinemia Acute lymphoblastic leukemia Mixed germ cell tumor of central nervous system Extracutaneous mastocytoma Mast cell leukemia X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Acute monoblastic/monocytic leukemia Hypereosinophilic syndrome Germinoma of the central nervous system Acute leukemia of ambiguous lineage Medulloepithelioma of the central nervous system Von Willebrand disease type 2N Rare hemorrhagic disorder due to an acquired coagulation factor defect Myeloid sarcoma Teratoma of the central nervous system Hemoglobin M disease MYH9-related disease Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome Acute myelomonocytic leukemia Nephroblastoma Tumor of meninges Acute megakaryoblastic leukemia Von Willebrand disease type 3 Sickle cell disease and related diseases Rare thrombotic disease of hematologic origin Acute myeloid leukemia Refractory anemia with excess blasts in transformation Oligodendroglial tumor Acute promyelocytic leukemia Plasmacytoma Chronic myeloid leukemia Composite lymphoma Rare hemorrhagic disorder due to an acquired platelet anomaly Familial hypofibrinogenemia Undifferentiated pleomorphic sarcoma Primary melanocytic tumor of central nervous system Benign schwannoma Langerhans cell histiocytosis Alpha granule disease Non-amyloid monoclonal immunoglobulin deposition disease Hereditary isolated aplastic anemia Choroid plexus tumor Heavy chain disease Classic Hodgkin lymphoma Juvenile hyaline fibromatosis Unstable hemoglobin disease Diffuse leptomeningeal melanocytosis Dense granule disease Congenital dyserythropoietic anemia type I Atypical papilloma of choroid plexus Vestibular schwannoma Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma Soft tissue sarcoma Fibrosarcoma Severe hemophilia B Sickle cell disease associated with another hemoglobin anomaly Persistent polyclonal B-cell lymphocytosis Transient erythroblastopenia of childhood Osteosarcoma Oligodendroglioma Methylcobalamin deficiency type cblE Idiopathic hypereosinophilic syndrome Congenital dyserythropoietic anemia type III Choroid plexus carcinoma Glial tumor Methylcobalamin deficiency type cblG Scott syndrome Diamond-Blackfan anemia Autoimmune lymphoproliferative syndrome Imerslund-Gräsbeck syndrome Bloom syndrome Low-grade ependymoma Hypoxanthine guanine phosphoribosyltransferase partial deficiency Congenital dyserythropoietic anemia type II Sebastian syndrome Aceruloplasminemia Mild hemophilia B Germ cell tumor Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma Pineal tumor of neuroepithelial tissue Primary acquired pure red cell aplasia Heavy chain deposition disease Rare thrombotic disorder due to a coagulation factors defect Sickle cell-beta-thalassemia disease syndrome Moderate hemophilia B Atypical teratoid rhabdoid tumor Acquired von Willebrand syndrome Anaplastic oligodendroglioma Severe hemophilia A Sickle cell-hemoglobin C disease syndrome Pleomorphic liposarcoma Neurofibroma Shwachman-Diamond syndrome Perineurioma Light chain deposition disease Adult T-cell leukemia/lymphoma Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Acute myeloid leukemia with t(8;16)(p11;p13) translocation Meningeal melanocytoma Myxoid/round cell liposarcoma Pineoblastoma Light and heavy chain deposition disease Well-differentiated liposarcoma Methylcobalamin deficiency type cblDv1 Familial afibrinogenemia Hemophilia B Primary cutaneous CD30+ T-cell lymphoproliferative disease Dedifferentiated liposarcoma Hemophilia A Rare thrombotic disorder due to a constitutional coagulation factors defect Primary cutaneous lymphoma Extranodal nasal NK/T cell lymphoma Papillary tumor of the pineal region Desmoplastic small round cell tumor Kaposi sarcoma Myxofibrosarcoma Rare thrombotic disorder due to a platelet anomaly Familial dysfibrinogenemia Primary melanoma of the central nervous system Rare nervous system tumor Primary cutaneous marginal zone B-cell lymphoma Primary cutaneous gamma/delta-positive T-cell lymphoma Pineocytoma Infantile myofibromatosis Synovial sarcoma Rare thrombotic disorder due to an acquired coagulation factors defect Moderate hemophilia A Bleeding diathesis due to integrin alpha2-beta1 deficiency Rare hemorrhagic disorder due to a constitutional coagulation factors defect Anaplastic ependymoma Immune thrombocytopenia Bernard-Soulier syndrome Pineal parenchymal tumor of intermediate differentiation X-linked sideroblastic anemia Non-Hodgkin lymphoma Dyskeratosis congenita Bleeding diathesis due to glycoprotein VI deficiency Primary cutaneous follicle center lymphoma Hemangioblastoma Mild hemophilia A Acquired idiopathic sideroblastic anemia Subcutaneous panniculitis-like T-cell lymphoma Sickle cell-hemoglobin D disease syndrome Primary cutaneous peripheral T-cell lymphoma not otherwise specified Oligoastrocytic tumor Primary cutaneous diffuse large B-cell lymphoma, leg type Primary myelofibrosis Autoimmune thrombocytopenia Mitochondrial myopathy and sideroblastic anemia Rare hemorrhagic disorder due to a constitutional platelet anomaly Tumor of cranial and spinal nerves Sickle cell-hemoglobin E disease syndrome Typical urticaria pigmentosa Indolent primary cutaneous T-cell lymphoma Extraventricular neurocytoma Nodular urticaria pigmentosa Malignant peripheral nerve sheath tumor East Texas bleeding disorder Plaque-form urticaria pigmentosa Rare soft tissue tumor Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome Systemic mastocytosis Nodular lymphocyte predominant Hodgkin lymphoma Autosomal dominant aplasia and myelodysplasia Extraskeletal myxoid chondrosarcoma Neuronal tumor Histiocytic sarcoma Tumor of hematopoietic and lymphoid tissues Smoldering systemic mastocytosis Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Cerebellar liponeurocytoma Central neurocytoma Dermatofibrosarcoma protuberans Pearson syndrome Langerhans cell sarcoma Non-seminomatous germ cell tumor of testis Oligoastrocytoma Plummer-Vinson syndrome Syndrome with alpha-thalassemia as a major feature Aggressive primary cutaneous T-cell lymphoma Primary oculocerebral lymphoma Primary hypereosinophilic syndrome Indolent primary cutaneous B-cell lymphoma Interdigitating dendritic cell sarcoma Anaplastic oligoastrocytoma Congenital epulis Congenital thrombotic thrombocytopenic purpura Pseudo-von Willebrand disease Mixed neuronal-glial tumor Constitutional anemia due to iron metabolism disorder Aggressive primary cutaneous B-cell lymphoma Isolated bone marrow mastocytosis Dendritic cell sarcoma not otherwise specified Acute myeloid leukemia with t(8;21)(q22;q22) translocation Multiple myeloma Rare anemia Immune-mediated thrombotic thrombocytopenic purpura Follicular dendritic cell sarcoma Hemoglobin D disease Congenital vitamin K-dependent coagulation factors deficiency Familial multiple meningioma Glial tumor of neuroepithelial tissue with unknown origin Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Constitutional sideroblastic anemia Familial thrombocytosis Desmoplastic infantile astrocytoma/ganglioglioma Ollier disease Methotrexate-associated lymphoproliferative disorders Testicular seminomatous germ cell tumor Gaisböck syndrome Malignant triton tumor Germ cell tumor of testis Reticular perineurioma Sézary syndrome Acquired prothrombin deficiency Rare hemolytic anemia Gangliocytoma Protein S acquired deficiency Methylmalonic acidemia with homocystinuria

Provided care options 3

# Contact person
1
Spezialambulanz für Gerinnungsstörungen
PD Dr. Monika Sparber-Sauer

0711 27872740
Website
Sprechzeiten: Do 8:00 - 16:00 Uhr.

2
Hämatologisch-onkologische Ambulanz
PD Dr. Claudia Blattmann

0711 27872740
Website
Sprechzeiten: Mo 13:30 – 14:30 Uhr und 15:00 - 16:00 Uhr sowie Do 9:30 – 11:00 Uhr und 14:00 – 16:00 Uhr nach Vereinbarung.

3
Spezialambulanz für Patienten mit Osteosarkom
Dr. Stefanie Hecker-Nolting, PD Dr. Monika Sparber-Sauer

0711 27872740
Website
Sprechzeiten: Di 8:00 - 16:00 Uhr nach Vereinbarung.

9.17324066162109648.7835472950952Pädiatrie 5 – Onkologie, Hämatologie und Immunologie am Klinikum Stuttgart
Last updated: 18.07.2023