A rare case of unexplained recurrent intracerebral haemorrhage
- PMID: 39925962
- PMCID: PMC11806917
- DOI: 10.1093/jscr/rjaf033
A rare case of unexplained recurrent intracerebral haemorrhage
Abstract
Recurrent intracerebral haemorrhage (ICH) presents a complex clinical challenge that eludes traditional diagnostic and treatment approaches. We report a rare and unexplained case of a middle-aged patient with recurrent ICH, for which extensive multidisciplinary investigations have yet to provide a definitive diagnosis or an effective long-term treatment strategy. Intraoperative pathology, genetic testing, cerebral angiography, inflammatory markers (erythrocyte sedimentation rate, C-reactive protein), specific antibodies (ANCA, anti-nuclear antibodies), and immunoglobulin levels showed no specific positive findings. This case highlights the limitations of current diagnostic and therapeutic modalities in recurrent ICH. Further research into the genetic and molecular underpinnings of recurrent ICH is needed to enhance diagnostic accuracy and develop targeted therapies for similar cases.
Keywords: case reports; cerebrovascular disease; neurosurgical interventions; rare cerebrovascular cases; recurrent intracerebral haemorrhage.
Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2025.
Conflict of interest statement
The authors declare no conflict of interest exits in the submission of this manuscript, and manuscript is approved by all authors for publication. I would like to declare on behalf of my co-authors that the work described was original research that has not been published previously, and not under consideration for publication elsewhere, in whole or in part. All the authors listed have approved the manuscript that is enclosed.
Figures





References
-
- Vignesh S, Prasad SN, Singh V, et al. Angiographic analysis on posterior fossa hemorrhages and vascular malformations beyond aneurysms by CT angiography and digital subtraction angiography. Egyptian J Neurosurg 2022;37:12.
Publication types
LinkOut - more resources
Full Text Sources
Research Materials