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  1. Book ; Thesis: hTERT-Promotor-Mutation und hTERT-Expression in Hepatozellulären Karzinomen

    Fischer, Anne Kristin / Vokuhl, Christian Oliver

    2022  

    Institution Rheinische Friedrich-Wilhelms-Universität Bonn
    Author's details Anne Kristin Fischer ; 1. Gutachter: Prof. Dr. med. Christian Oliver Vokuhl
    Language German
    Size 91 Seiten, Illustrationen, Diagramme
    Publishing place Bonn
    Publishing country Germany
    Document type Book ; Thesis
    Thesis / German Habilitation thesis Dissertation, Rheinische Friedrich-Wilhelms-Universität Bonn, 2022
    HBZ-ID HT021380961
    Database Catalogue ZB MED Medicine, Health

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  2. Article ; Online: Kindliche Tumoren – eine kurze Einführung zum Thema.

    Vokuhl, Christian

    Pathologie (Heidelberg, Germany)

    2023  Volume 44, Issue 6, Page(s) 336–337

    Title translation Pediatric tumors-a short introduction to the topic.
    MeSH term(s) Child ; Humans ; Neoplasms
    Language German
    Publishing date 2023-10-26
    Publishing country Germany
    Document type Editorial
    ISSN 2731-7196
    ISSN (online) 2731-7196
    DOI 10.1007/s00292-023-01236-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Periphere neuroblastische Tumoren im Kindesalter.

    Bernhardt, Marit / Vokuhl, Christian

    Pathologie (Heidelberg, Germany)

    2023  Volume 44, Issue 6, Page(s) 366–372

    Abstract: Peripheral neuroblastic tumors represent the fourth-largest group of malignant tumors in childhood. The majority of these tumors are neuroblastomas, which can be classified into undifferentiated, poorly differentiated, and differentiating subtypes. In ... ...

    Title translation Peripheral neuroblastic tumors in childhood.
    Abstract Peripheral neuroblastic tumors represent the fourth-largest group of malignant tumors in childhood. The majority of these tumors are neuroblastomas, which can be classified into undifferentiated, poorly differentiated, and differentiating subtypes. In addition, peripheral neuroblastic tumors include ganglioneuroblastoma, a composite tumor composed of Schwannian cell stroma and neuroblasts as well as benign ganglioneuroma. In this overview, histopathological diagnostic criteria and grading systems, as well as common molecular alterations that are of prognostic and therapeutic significance, are discussed.
    MeSH term(s) Humans ; Neuroblastoma/diagnosis ; Ganglioneuroblastoma/diagnosis ; Prognosis ; Ganglioneuroma/diagnosis ; Stromal Cells/pathology ; Neuroectodermal Tumors, Primitive
    Language German
    Publishing date 2023-10-11
    Publishing country Germany
    Document type English Abstract ; Journal Article ; Review
    ISSN 2731-7196
    ISSN (online) 2731-7196
    DOI 10.1007/s00292-023-01227-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Rezeptor-Tyrosinkinase-Fusionen in spindelzelligen Tumoren des Kindesalters.

    Brenner, Christiane / Sanders, Christine / Vokuhl, Christian

    Pathologie (Heidelberg, Germany)

    2023  Volume 44, Issue 6, Page(s) 357–365

    Abstract: Pediatric spindle cell tumors are rare and often difficult to diagnose due to a similar morphology and a non-specific immunohistochemical profile. Genetic characterization of these lesions has been constantly improving, which has led to the ... ...

    Title translation Receptor tyrosine kinase- fusions in paediatric spindle cell tumors.
    Abstract Pediatric spindle cell tumors are rare and often difficult to diagnose due to a similar morphology and a non-specific immunohistochemical profile. Genetic characterization of these lesions has been constantly improving, which has led to the identification of new subgroups that were partly included in the WHO classification. Receptor tyrosine kinase fusions play a special role in these tumors and their verification has diagnostic relevance and can be an option for target-oriented therapies. In the case of pediatric spindle cell tumors, genetic fusions form especially with NTRK1‑3, ALK, RET, and ROS1. Overall, pediatric tumors with receptor tyrosine kinase fusions are predominantly low-grade tumors, which are often subdivided into the group of intermediate-malign tumors.
    MeSH term(s) Humans ; Child ; Protein-Tyrosine Kinases/genetics ; Anaplastic Lymphoma Kinase/genetics ; Proto-Oncogene Proteins/genetics ; Receptor Protein-Tyrosine Kinases/genetics ; Lung Neoplasms/genetics
    Chemical Substances Protein-Tyrosine Kinases (EC 2.7.10.1) ; Anaplastic Lymphoma Kinase (EC 2.7.10.1) ; Proto-Oncogene Proteins ; Receptor Protein-Tyrosine Kinases (EC 2.7.10.1)
    Language German
    Publishing date 2023-10-11
    Publishing country Germany
    Document type English Abstract ; Journal Article ; Review
    ISSN 2731-7196
    ISSN (online) 2731-7196
    DOI 10.1007/s00292-023-01228-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Stemness Correlates Inversely with MHC Class I Expression in Pediatric Small Round Blue Cell Tumors.

    Müller, Linda / Kschischo, Maik / Vokuhl, Christian / Stahl, David / Gütgemann, Ines

    Cancers

    2022  Volume 14, Issue 15

    Abstract: Recently, immunotherapeutic approaches have become a feasible option for a subset of pediatric cancer patients. Low MHC class I expression hampers the use of immunotherapies relying on antigen presentation. A well-established stemness score (mRNAsi) was ... ...

    Abstract Recently, immunotherapeutic approaches have become a feasible option for a subset of pediatric cancer patients. Low MHC class I expression hampers the use of immunotherapies relying on antigen presentation. A well-established stemness score (mRNAsi) was determined using the bulk transcriptomes of 1134 pediatric small round blue cell tumors. Interestingly, MHC class I gene expression (HLA-A/-B/-C) was correlated negatively with mRNAsi throughout all diagnostic entities: neuroblastomas (NB) (n = 88, r = −0.41, p < 0.001), the Ewing’s sarcoma family of tumors (ESFT) (n = 117, r = −0.46, p < 0.001), rhabdomyosarcomas (RMS) (n = 158, r = −0.5, p < 0.001), Wilms tumors (WT) (n = 224, r = −0.39, p < 0.001), and central nervous system-primitive neuroectodermal tumors CNS-PNET (r = −0.49, p < 0.001), with the exception of medulloblastoma (MB) (n = 76, r = −0.24, p = 0.06). The negative correlation of MHC class I and mRNAsi was independent of clinical features in NB, RMS, and WT. In NB and WT, increased MHC class I was correlated negatively with tumor stage. RMS patients with a high expression of MHC class I and abundant CD8 T cells showed a prolonged overall survival (n = 148, p = 0.004). Possibly, low MHC class I expression and stemness in pediatric tumors are remnants of prenatal tumorigenesis from multipotent precursor cells. Further studies are needed to assess the usefulness of stemness and MHC class I as predictive markers.
    Language English
    Publishing date 2022-07-22
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers14153584
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: A multi-step approach to the treatment of giant scalp congenital hemangiomas: a report of two cases.

    Ho, Raymond W / Nonnenmacher, Gabriel / Henkes, Hans / Vokuhl, Christian / Loff, Steffan

    Frontiers in surgery

    2023  Volume 10, Page(s) 1045285

    Abstract: This is a review of two cases of neonatal giant scalp congenital hemangioma. Both patients were treated with propranolol using a similar multi-step approach that included transarterial embolization of the supplying arteries followed by surgical resection ...

    Abstract This is a review of two cases of neonatal giant scalp congenital hemangioma. Both patients were treated with propranolol using a similar multi-step approach that included transarterial embolization of the supplying arteries followed by surgical resection of the lesion. In this report, we discuss the treatments, complications, and clinical outcomes of interventions and surgical procedures.
    Language English
    Publishing date 2023-05-24
    Publishing country Switzerland
    Document type Case Reports
    ZDB-ID 2773823-1
    ISSN 2296-875X
    ISSN 2296-875X
    DOI 10.3389/fsurg.2023.1045285
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Lymph node metastases are more frequent in paediatric appendiceal NET ≥1.5 cm but without impact on outcome - Data from the German MET studies.

    Kuhlen, Michaela / Kunstreich, Marina / Pape, Ulrich-Frank / Seitz, Guido / Lessel, Lienhard / Vokuhl, Christian / Frühwald, Michael C / Vorwerk, Peter / Redlich, Antje

    European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology

    2024  Volume 50, Issue 4, Page(s) 108051

    Abstract: Background: Paediatric appendiceal neuroendocrine tumours (appNET) are very rare tumours, mostly detected incidentally by histopathological evaluation after appendectomy. Treatment recommendations are based on adult data considering high-risk NET as ... ...

    Abstract Background: Paediatric appendiceal neuroendocrine tumours (appNET) are very rare tumours, mostly detected incidentally by histopathological evaluation after appendectomy. Treatment recommendations are based on adult data considering high-risk NET as defined by European Neuroendocrine Tumour Society (ENETS) guidelines for completion right-sided hemicolectomy (RHC). Recent data suggest that less aggressive therapy may be justified.
    Procedure: Analysis of children and adolescents with appNET prospectively registered with the German Malignant Endocrine Tumour (MET) studies between 1997 and 2022.
    Results: By December 2022, 662 patients (64.7% females, 35.3% male) had been reported. Median age was 13.3 years [4.5-17.9], median duration of follow-up 2.2 years [0-10.9]. No distant metastases were reported. Tumour size was <1 cm in 63.5%, 1-2 cm in 33.2%, and >2 cm in 3.2% of patients. WHO grade 1 and 2 tumours were diagnosed in 76.9% and 23.1% of patients, respectively. Lymphovascular invasion and lymph node metastases were associated with tumour size ≥1.5 cm. 27.0% of patients presented with high-risk NET according to ENETS criteria. Of those, only 55.9% underwent secondary oncological right hemicolectomy. Neither distant metastases, nor recurrences or disease-related deaths occurred in patients with appendectomy only as well as in patients with completion RHC. Overall and event-free survival were both 100%.
    Conclusions: Internationally harmonized consensus recommendations on treatment of children and adolescents with appendiceal NET are urgently needed to avoid completion RHC in high-risk patients.
    MeSH term(s) Adult ; Female ; Adolescent ; Humans ; Male ; Child ; Lymphatic Metastasis ; Neuroendocrine Tumors/pathology ; Appendiceal Neoplasms/pathology ; Appendectomy ; Endocrine Gland Neoplasms/surgery ; Colectomy ; Retrospective Studies ; Intestinal Neoplasms ; Pancreatic Neoplasms ; Stomach Neoplasms
    Language English
    Publishing date 2024-02-27
    Publishing country England
    Document type Journal Article
    ZDB-ID 632519-1
    ISSN 1532-2157 ; 0748-7983
    ISSN (online) 1532-2157
    ISSN 0748-7983
    DOI 10.1016/j.ejso.2024.108051
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Pathology of Hepatocellular Carcinoma and Tumor-Bearing Liver Tissue in Association with

    Fischer, Anne Kristin / Semaan, Alexander / Wulf, Anna-Lena / Vokuhl, Christian / Goltz, Diane / Fischer, Hans-Peter

    International journal of hepatology

    2023  Volume 2023, Page(s) 4313504

    Abstract: Background: The : Methods: The study cohort comprised 160 histologically confirmed HCC in patients with or without cirrhosis that were investigated for the : Results: The : Conclusions: Our study reveals a connection between pathological ... ...

    Abstract Background: The
    Methods: The study cohort comprised 160 histologically confirmed HCC in patients with or without cirrhosis that were investigated for the
    Results: The
    Conclusions: Our study reveals a connection between pathological changes in tumor-bearing liver tissue and the
    Language English
    Publishing date 2023-08-09
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2621468-4
    ISSN 2090-3456 ; 2090-3448
    ISSN (online) 2090-3456
    ISSN 2090-3448
    DOI 10.1155/2023/4313504
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Dataset for the reporting of nephrectomy specimens for Wilms' tumour treated with preoperative chemotherapy: recommendations from the International Society of Paediatric Oncology Renal Tumour Study Group.

    Vujanić, Gordan M / D'Hooghe, Ellen / Vokuhl, Christian / Collini, Paola

    Histopathology

    2021  Volume 79, Issue 5, Page(s) 678–686

    Abstract: Datasets for histopathological reporting of many cancer types are developed by the International Collaboration on Cancer Reporting (ICCR), and are used in order to ensure standardised and uniformly accepted reporting as one of the essential requirements ... ...

    Abstract Datasets for histopathological reporting of many cancer types are developed by the International Collaboration on Cancer Reporting (ICCR), and are used in order to ensure standardised and uniformly accepted reporting as one of the essential requirements for comparison across patient populations in evaluating and validating pathological prognostic and predictive factors. Wilms' tumours are rare, and international reporting guidelines have not yet been published by the ICCR. The assessment of Wilms' tumours differs according to the treatment approach. The Children's Oncology Group, whose approach is followed mainly in North America, advocates primary surgery, and the International Society of Paediatric Oncology Renal Tumour Study Group (SIOP-RTSG), whose approach is followed in most countries around the world, uses preoperative chemotherapy as a first step, resulting in different subclassifications, staging criteria, and histopathological prognostic factors. This dataset is developed for the countries and institutions following the SIOP-RTSG approach, and it contains core (required) and non-core (recommended) elements, based on the results of the previous SIOP-RTSG studies, which are incorporated in the latest SIOP-RTSG UMBRELLA 2016 Study protocol. The core elements include clinical information, additional specimen submitted, macroscopic tumour site and appearance, tumour focality, tumour dimensions, macroscopic extent of invasion, block identification key, histological tumour type, histological tumour grade and risk group assessment, microscopic extent of invasion, lymphovascular invasion, resection margin status, regional lymph node status, histologically confirmed distant metastases, and pathological staging (SIOP staging system). The dataset should improve communication for patient care and prognostic determination of the old and new histopathological features.
    MeSH term(s) Datasets as Topic ; Drug Therapy ; Humans ; Kidney Neoplasms/pathology ; Medical Oncology/standards ; Neoplasm Grading/methods ; Neoplasm Staging/methods ; Nephrectomy ; North America ; Prognosis ; Risk Factors ; Wilms Tumor/classification ; Wilms Tumor/pathology
    Language English
    Publishing date 2021-07-08
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 131914-0
    ISSN 1365-2559 ; 0309-0167
    ISSN (online) 1365-2559
    ISSN 0309-0167
    DOI 10.1111/his.14394
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: New

    Theis, Bernhard / Alhussami, Ilmi / Kämmerer, Elke / Kentouche, Karim / Vokuhl, Christian / Gassler, Nikolaus / Katenkamp, Kathrin

    International journal of clinical and experimental pathology

    2022  Volume 15, Issue 10, Page(s) 425–430

    Abstract: The histomorphology of liboblastoma is highly variable and comprises different patterns that are found admixed or in pure form within a tumor. The most important features - mature lipomatous, fibrotic, lipofibrous, and myxoid - overlap with the ... ...

    Abstract The histomorphology of liboblastoma is highly variable and comprises different patterns that are found admixed or in pure form within a tumor. The most important features - mature lipomatous, fibrotic, lipofibrous, and myxoid - overlap with the histomorphology of several other pediatric tumor entities. Regarding the morphologic overlaps, molecular diagnostics with identification of fusion transcripts involving
    Language English
    Publishing date 2022-10-15
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2418306-4
    ISSN 1936-2625 ; 1936-2625
    ISSN (online) 1936-2625
    ISSN 1936-2625
    Database MEDical Literature Analysis and Retrieval System OnLINE

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