Spontaneous Subdural Hemorrhage in a Patient with Marfan Syndrome: Case Report and Literature Review

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.

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Journal
Journal of Endovascular Resuscitation and Trauma Management
Published
2025-09-16
DOI
https://doi.org/10.26676/jevtm.40918
Primary Topic
Neurosurgical Procedures and Complications
Type
article
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article

Spontaneous Subdural Hemorrhage in a Patient with Marfan Syndrome: Case Report and Literature Review

Egor Chmutin, Bipin Chaurasia, İsmail Bozkurt, Daniel Encarnación-Santos et al.
Journal of Endovascular Resuscitation and Trauma Management
Neurosurgical Procedures and Complications
article

Spontaneous Subdural Hemorrhage in a Patient with Marfan Syndrome: Case Report and Literature Review

Egor Chmutin, Bipin Chaurasia, İsmail Bozkurt, Daniel Encarnación-Santos, Eugeny Shestov, Gennady Chmutin, Murat Pachev, Dmitriy Rubenovich-Chikava, Emmanuel Batista-Geraldino, Marina Axenova, Ahmad Rami Kassar
article en

Abstract

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.

Journal of Endovascular Resuscitation and Trauma ManagementVol. 9(2)
Peoples' Friendship University of Russia (RU), Bir Hospital (NP), Hospital San Juan de la Cruz (ES), City Clinical Hospital No. 2 (RU), Yüksek İhtisas Üniversitesi (TR)
Openalex Percentile: Top 64%
Neurosurgical Procedures and Complications
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Spontaneous Subdural Hemorrhage in a Patient with Marfan Syndrome: Case Report and Literature Review — Egor Chmutin, Bipin Chaurasia, et al. · Journal of Endovascular Resuscitation and Trauma Management (2025) | TGRS Research Map | TGRS