Skip to main content

and
  1. No Access

    Article

    Lymph node staging with fluorine-18 prostate specific membrane antigen 1007-positron emission tomography/computed tomography in newly diagnosed intermediate- to high-risk prostate cancer using histopathological evaluation of extended pelvic node dissection as reference

    Fluorine-18 (18F) prostate–specific membrane antigen (PSMA) 1007 (18F-PSMA-1007) is a radiotracer used in prostate cancer (PCa) staging. So far, no large histopathological validation study has been conducted. The...

    Rick Hermsen, Esmée B. C. Wedick in European Journal of Nuclear Medicine and M… (2022)

  2. Article

    Open Access

    Poor outcome in hypoxic endometrial carcinoma is related to vascular density

    Identification of endometrial carcinoma (EC) patients at high risk of recurrence is lacking. In this study, the prognostic role of hypoxia and angiogenesis was investigated in EC patients.

    Casper Reijnen, Willem Jan van Weelden, Martijn S. J. P. Arts in British Journal of Cancer (2019)

  3. No Access

    Article

    Whole-exome sequencing of a meningeal melanocytic tumour reveals activating CYSLTR2 and EIF1AX hotspot mutations and similarities to uveal melanoma

    Heidi V. N. Küsters-Vandevelde, Menno R. Germans, Roy Rabbie in Brain Tumor Pathology (2018)

  4. No Access

    Article

    Copy number variations as potential diagnostic and prognostic markers for CNS melanocytic neoplasms in neurocutaneous melanosis

    Adriana C. H. van Engen-van Grunsven, Katrin Rabold in Acta Neuropathologica (2017)

  5. Article

    Open Access

    SF3B1 and EIF1AX mutations occur in primary leptomeningeal melanocytic neoplasms; yet another similarity to uveal melanomas

    Like uveal melanomas, primary leptomeningeal melanocytic neoplasms (LMNs) frequently carry GNAQ and GNA11 mutations. However, it is currently unknown whether these LMNs harbor mutations in BAP1, SF3B1 and/or EIF1...

    Heidi V. N. Küsters-Vandevelde, David Creytens in Acta Neuropathologica Communications (2016)

  6. No Access

    Article

    Mutations in G Protein Encoding Genes and Chromosomal Alterations in Primary Leptomeningeal Melanocytic Neoplasms

    Limited data is available on the genetic features of primary leptomeningeal melanocytic neoplasms (LMNs). Similarities with uveal melanoma were recently suggested as both entities harbor oncogenic mutations in GN...

    Heidi V. N. Küsters-Vandevelde in Pathology & Oncology Research (2015)

  7. Article

    Open Access

    Improved discrimination of melanotic schwannoma from melanocytic lesions by combined morphological and GNAQ mutational analysis

    The histological differential diagnosis between melanotic schwannoma, primary leptomeningeal melanocytic lesions and cellular blue nevus can be challenging. Correct diagnosis of melanotic schwannoma is importa...

    Heidi V. N. Küsters-Vandevelde in Acta Neuropathologica (2010)

  8. Article

    Open Access

    Activating mutations of the GNAQ gene: a frequent event in primary melanocytic neoplasms of the central nervous system

    Primary melanocytic neoplasms of the central nervous system (CNS) are uncommon neoplasms derived from melanocytes that normally can be found in the leptomeninges. They cover a spectrum of malignancy grades ran...

    Heidi V. N. Küsters-Vandevelde, Annelies Klaasen, Benno Küsters in Acta Neuropathologica (2010)

  9. Article

    Open Access

    Occurrence of ocular melanoma thirteen years after skin melanoma: two separate primaries or metastatic disease? A case solved with NRAS and CDKN2A (INK4A-ARF) mutational analysis

    The differential diagnosis between primary uveal melanoma and cutaneous melanoma metastasis in the eye may be difficult, both clinically and histologically. We report successful application of combined mutatio...

    Heidi V. N. Küsters-Vandevelde, Jan E. E. Keunen, Pieter Wesseling in Virchows Archiv (2008)