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Dysembryoplastic Neuroepithelial Tumors
Yeon-Lim Suh
J Pathol Transl Med. 2015;49(6):438-449.   Published online October 23, 2015
DOI: https://doi.org/10.4132/jptm.2015.10.05
  • 11,546 View
  • 252 Download
  • 17 Web of Science
  • 20 Crossref
AbstractAbstract PDF
Dysembryoplastic neuroepithelial tumor (DNT) is a benign glioneuronal neoplasm that most commonly occurs in children and young adults and may present with medically intractable, chronic seizures. Radiologically, this tumor is characterized by a cortical topography and lack of mass effect or perilesional edema. Partial complex seizures are the most common presentation. Three histologic subtypes of DNTs have been described. Histologically, the recognition of a unique, specific glioneuronal element in brain tumor samples from patients with medically intractable, chronic epilepsy serves as a diagnostic feature for complex or simple DNT types. However, nonspecific DNT has diagnostic difficulty because its histology is indistinguishable from conventional gliomas and because a specific glioneuronal element and/or multinodularity are absent. This review will focus on the clinical, radiographic, histopathological, and immunohistochemical features as well as the molecular genetics of all three variants of DNTs. The histological and cytological differential diagnoses for this lesion, especially the nonspecific variant, will be discussed.

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  • Clinicopathological features of dysembryoplastic neuroepithelial tumor: a case series
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Brief Case Reports
Supratentorial Hemangioblastoma with Unusual Features
Yooju Shin, Seokhwi Kim, Hyun-Woo Lee, Heejin Bang, Yeon-Lim Suh
Korean J Pathol. 2014;48(6):462-465.   Published online December 31, 2014
DOI: https://doi.org/10.4132/KoreanJPathol.2014.48.6.462
  • 9,867 View
  • 61 Download
  • 6 Crossref
PDF

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  • Supratentorial Hemangioblastoma in Adults: A Systematic Review and Comparison of Infratentorial and Spinal Cord Locations
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  • Supratentorial hemangioblastoma: correlation between phenotype, gender and vascular territory affected
    Yosef Laviv, David Saraf, Liat Oxman, Ido Ben Zvi
    Neurosurgical Review.2023;[Epub]     CrossRef
  • Neuropathologic features of central nervous system hemangioblastoma
    Rebecca A. Yoda, Patrick J. Cimino
    Journal of Pathology and Translational Medicine.2022; 56(3): 115.     CrossRef
  • The loss of succinate dehydrogenase B expression is frequently identified in hemangioblastoma of the central nervous system
    Tae Hoon Roh, Hyunee Yim, Jin Roh, Kyi Beom Lee, So Hyun Park, Seon-Yong Jeong, Se-Hyuk Kim, Jang-Hee Kim
    Scientific Reports.2019;[Epub]     CrossRef
  • Supratentorial hemangioblastomas in von Hippel–Lindau wild-type patients – case series and literature review
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  • MR Imaging Findings of Supratentorial Meningeal Hemangioblastoma: A Case Report
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Chordoid Meningioma in a Pediatric Patient with Tuberous Sclerosis Complex
Jiwon Lee, Hee Joon Yu, Jeehun Lee, Ji Hye Kim, Hyung Jin Shin, Yeon-Lim Suh, Munhyang Lee
Korean J Pathol. 2014;48(4):302-306.   Published online August 26, 2014
DOI: https://doi.org/10.4132/KoreanJPathol.2014.48.4.302
  • 7,384 View
  • 34 Download
  • 3 Crossref
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Citations

Citations to this article as recorded by  
  • Somatic mutation landscape in a cohort of meningiomas that have undergone grade progression
    Sarah A Cain, Bernard Pope, Stefano Mangiola, Theo Mantamadiotis, Katharine J Drummond
    BMC Cancer.2023;[Epub]     CrossRef
  • Innumerable Meningiomas Arising in a Patient With Tuberous Sclerosis Complex Decades After Radiation Therapy
    Ahmed Gilani, Julieann C Lee, BK Kleinschmidt-DeMasters
    Pediatric and Developmental Pathology.2021; 24(5): 471.     CrossRef
  • Predictors of recurrence in the management of chordoid meningioma
    Winward Choy, Leonel Ampie, Jonathan B. Lamano, Kartik Kesavabhotla, Qinwen Mao, Andrew T. Parsa, Orin Bloch
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Original Article
Morphologic Alteration of Metastatic Neuroblastic Tumor in Bone Marrow after Chemotherapy
Go Eun Bae, Yeon-Lim Suh, Ki Woong Sung, Jung-Sun Kim
Korean J Pathol. 2013;47(5):433-442.   Published online October 25, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.5.433
  • 6,369 View
  • 38 Download
  • 1 Crossref
AbstractAbstract PDF
Background

The aim of this study is to evaluate the histologic features of metastatic neuroblastic tumors (NTs) in bone marrow (BM) before and after chemotherapy in comparison with those of primary NTs.

Methods

A total of 294 biopsies from 48 children diagnosed with NTs with BM metastasis were examined. There were 48 primary neoplasm biopsies, 48 BM biopsies before chemotherapy, 36 primary neoplasm excisional biopsies after chemotherapy, and 162 BM biopsies after chemotherapy.

Results

Metastatic NTs in BM before chemotherapy were composed of undifferentiated and/or differentiating neuroblasts, but had neither ganglion cells nor Schwannian stroma. Metastatic foci of BM after chemotherapy were found to have differentiated into ganglion cells or Schwannian stroma, which became more prominent after further cycles of chemotherapy. Persistence of NTs or tumor cell types in BM after treatment did not show statistically significant correlation to patients' outcome. However, three out of five patients who newly developed poorly differentiated neuroblasts in BM after treatment expired due to disease progression.

Conclusions

Metastatic NTs in BM initially consist of undifferentiated or differentiating neuroblasts regardless of the primary tumor subtype, and become differentiated after chemotherapy. Newly appearing poorly differentiated neuroblasts after treatment might be an indicator for poor prognosis.

Citations

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  • Postchemotherapy gross residual tumor in non‐high‐risk neuroblastoma: Clinical significance and the role of adjuvant therapy
    Eun Seop Seo, Hana Lim, Hee Won Cho, Hee Young Ju, Ji Won Lee, Keon Hee Yoo, Sanghoon Lee, Do Hoon Lim, Ki Woong Sung, Hong Hoe Koo
    Pediatric Blood & Cancer.2022;[Epub]     CrossRef

J Pathol Transl Med : Journal of Pathology and Translational Medicine