A 36-year-old white man presented with sudden-onset headache and rapid deterioration of consciousness. Computer tomography revealed a right capsular intra-parenchimal hemorrhage with an intraventricular component; therefore, emergency surgery was performed. Once the hematoma was evacuated, the cause of the hemorrhage was identified as a tumor mass and it was resected. Histopathological and immunohistochemical examinations of the surgical specimen disclosed a diagnosis of atypical central neurocytoma. By using a protocol recently set up in our laboratory, we succeeded in isolating and propagating, for the first time, human endothelial cells from central neurocytoma (CN-ECs). Different analyses revealed that isolated CN-ECs consist of a pure endothelial cell population, with the expression of endothelial markers (CD31, CD309/VEGFR2, CD105, eNOS) and with angiogenic properties, such as the uptake of LDL. Moreover, CN-ECs spontaneously organize in a vascular-like structure. The goal of this case report is to stress the need for further studies focused on understanding the causes of the onset of an intra-parenchimal hemorrhage in the presence of an atypical central neurocytoma in order to tailor treatments to each single patient and achieve the best clinical outcome.

Download full-text PDF

Source
http://dx.doi.org/10.14670/HH-11-953DOI Listing

Publication Analysis

Top Keywords

central neurocytoma
16
atypical central
12
endothelial cells
8
intra-parenchimal hemorrhage
8
spontaneous intracerebral
4
hemorrhage
4
intracerebral hemorrhage
4
hemorrhage presentation
4
presentation atypical
4
central
4

Similar Publications

Extraventricular neurocytoma (EVN) is a rare neuronal tumor with a marked tendency towards ganglionic or glial differentiation. Although EVN commonly occurs in young adults, congenital cases are extremely rare, and standardized therapeutic strategies remain undetermined. The presence of atypical features such as increased mitotic activity on histological analysis is correlated with a higher rate of recurrence and poor prognosis.

View Article and Find Full Text PDF

Central Neurocytoma in a Teenager, a Rare Cause of Hemiplegia, and a Diagnostic Dilemma in a Resource-Poor Setting.

Case Rep Pathol

March 2024

Department of Pathology, School of Medical Sciences, University of Cape Coast, Cape Coast Teaching Hospital, Cape Coast, Ghana.

Article Synopsis
  • - Central neurocytoma is a benign brain tumor commonly found in the lateral ventricles, leading to symptoms like headaches and visual issues, particularly in young patients.
  • - An 18-year-old male presented with serious symptoms including seizures and unconsciousness, but due to the healthcare limitations, imaging studies weren’t conducted before his passing; an autopsy later confirmed the diagnosis of central neurocytoma.
  • - The study highlights challenges in differentiating central neurocytoma from other similar tumors, emphasizing the importance of specific lab tests to guide treatment and predict outcomes.
View Article and Find Full Text PDF

We report a case of neurocytoma originating from cranial nerve V. A 53-year-old female patient presented with a 20-day history of right frontotemporal facial paresthesia and pain. Magnetic resonance imaging (MRI) showed a 2.

View Article and Find Full Text PDF

Almost any primary or metastatic brain tumour can manifest in intraventricular (IV) locations. These tumours may either originate within the ventricular system or extend into the IV space through growth. Such neoplasms represent a broad spectrum, with supratentorial IV tumours forming a heterogeneous group.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!