Spontaneous Subdural Hemorrhage in a Patient with Marfan Syndrome: Case Report and Literature Review
DOI:
https://doi.org/10.26676/jevtm.40918Keywords:
Marfan Syndrome, Acute Subdural Hematoma, Neurological Complications, Surgical Intervention, Multidisciplinary ApproachAbstract
Background: Marfan syndrome is autosomal dominant with ocular, cardiovascular, and musculoskeletal manifestations. It is caused by mutation that encodes the fibrin gene on chromosome 15.
Case Presentation: A 54-year-old man presented to our center with a sudden onset of severe headache followed by a gradual loss of consciousness. His medical history was significant for Marfan syndrome. We found a spontaneous subdural hematoma in the left frontoparietotemporal area. The patient underwent emergency surgical intervention consisting of excision of the acute lesion and decompressive craniectomy in the left frontoparietal-temporal area. A postoperative brain computed tomography scan was conducted, which revealed a reduced midline shift and a subdural hematoma drainage. Laboratory investigations and intensive treatment were continued; however, the patient’s clinical condition deteriorated progressively.
Conclusion: This case underscores the rare occurrence of spontaneous acute subdural hematoma in the setting of Marfan syndrome, which calls for prompt recognition and surgical intervention.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2025 Daniel Antonio Encarnación-Santos, Dmitriy Rubenovich-Chikava, Murat Pachev, Eugeny Shestov, Ismail Bozkurt, Gennady Chmutin, Egor Chmutin, Ahmad Kassar, Marina Axenova, Bipin Chaurasia, Emmanuel Batista-Geraldino

This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors of content published in the JEVTM retain the copyright to their works.
Articles in the JEVTM are published under the terms of a Creative Commons CC BY 4.0 license, which permits use, downloading, distribution, linking to and reproduction in any medium, provided the original work is properly cited.

