Literature DB >> 26059172

Recurrent subependymoma of fourth ventricle with unusual atypical histological features: A case report.

Nishant Tiwari1, Suzanne Z Powell2, Hidehiro Takei2.   

Abstract

Subependymoma is a rare subtype of benign ependymal neoplasm with distinct histological features. Anaplastic transformation has not yet been reported in this tumor to date. We present here a very unusual case of a 62-year-old woman with recurrent subependymoma of the fourth ventricle with multiple atypical histological features. Histologically, the resected recurrent tumor showed characteristic small cell clusters and nests of ependymal cells with an interspersed gliofibrillary matrix as seen in a classic subependymoma. In addition, there were very unusual histological features, including multiple areas of necrosis, microvascular proliferation, thrombosed blood vessels, and scattered mitotic figures. No coexisting ependymoma component of higher World Health Organization (WHO) grade was present. Immunohistochemically, MIB-1 labeling index was high, with up to 15% in the highest areas. Review of this patient's initial tumor, which was resected 6 years prior to recurrence, demonstrated features of a typical classic subependymoma without atypical features or a secondary tumor component. Subependymomas are known to be low-grade tumors and are usually cured if completely excised. The tumor presented here is unique in that several atypical pathological features were found in an otherwise typical subependymoma. Our case may represent anaplastic transformation of subependymoma, although no such examples have been reported to date.
© 2015 Japanese Society of Pathology and Wiley Publishing Asia Pty Ltd.

Entities:  

Keywords:  anaplastic transformation; atypical pathologic features; brain; recurrence; subependymoma

Mesh:

Year:  2015        PMID: 26059172     DOI: 10.1111/pin.12316

Source DB:  PubMed          Journal:  Pathol Int        ISSN: 1320-5463            Impact factor:   2.534


  4 in total

1.  Bilateral lateral ventricular subependymoma with extensive multiplicity presenting with hemorrhage.

Authors:  F M Moinuddin; Novita Ikbar Khairunnisa; Hirofumi Hirano; Tomoko Hanada; Tsubasa Hiraki; Mari Kirishima; Kiyohisa Kamimura; Kazunori Arita
Journal:  Neuroradiol J       Date:  2017-07-11

2.  TERT promoter mutation and chromosome 6 loss define a high-risk subtype of ependymoma evolving from posterior fossa subependymoma.

Authors:  Christian Thomas; Felix Thierfelder; Malte Träger; Patrick Soschinski; Michael Müther; Dominic Edelmann; Alexandra Förster; Carola Geiler; Hee-Yeong Kim; Katharina Filipski; Patrick N Harter; Jens Schittenhelm; Franziska Eckert; Georgios Ntoulias; Sven-Axel May; Walter Stummer; Julia Onken; Peter Vajkoczy; Ulrich Schüller; Frank L Heppner; David Capper; Arend Koch; David Kaul; Werner Paulus; Martin Hasselblatt; Leonille Schweizer
Journal:  Acta Neuropathol       Date:  2021-03-23       Impact factor: 17.088

3.  Intraparenchymal subependymoma: Case report and literature review.

Authors:  Othavio Gomes Lopes; Felipe Calmon Du Pin Almeida; Gustavo Augusto Porto Sereno Cabral; Rodrigo Dias Guimaraes; Ruy Castro Monteiro da Silva Filho; Jose Alberto Landeiro
Journal:  Surg Neurol Int       Date:  2021-04-14

4.  Clinical independent prognostic factors and overall survival prognostic nomogram for intracranial subependymoma: A SEER population-based analysis 2004-2016.

Authors:  Zibin Zhang; Xiaojun Pang; Yuyu Wei; Qingping Lv; Xuhong Jin; Huai Chen
Journal:  Front Oncol       Date:  2022-08-22       Impact factor: 5.738

  4 in total

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