Your new experience awaits. Try the new design now and help us make it even better

CASE REPORT article

Front. Surg., 24 October 2025

Sec. Neurosurgery

Volume 12 - 2025 | https://doi.org/10.3389/fsurg.2025.1643743

Acute brain swelling due to intraoperative supratentorial subdural hematoma during microvascular decompression: a case report


Jia ShiJia ShiJiachao CaoJiachao CaoQiang Zhou

Qiang Zhou*
  • Department of Neurosurgery, The Third Affiliated Hospital of Soochow University, Changzhou, China

Background: Microvascular decompression (MVD) is the primary treatment for cranial neurovascular compression syndromes. The most critical complication is hemorrhage during or after surgery. Although intraoperative supratentorial subdural hematoma (SDH) is uncommon, its management remains complex and lacks standardization.

Case presentation: We report a case of acute brain swelling caused by an intraoperative supratentorial subdural hematoma during microvascular decompression (MVD) for trigeminal neuralgia. By effectively managing intracranial pressure and preventing secondary brain injury, the operation was successfully completed, resulting in a favorable postoperative recovery for the patient.

Conclusion: This study examines the presentation and management of acute brain swelling caused by intraoperative supratentorial subdural hematoma (SDH). We aim to highlight the importance of being vigilant for this rare complication during microvascular decompression (MVD), as it can result in fatal brain swelling and encephalocele. Preventing and managing this severe complication remains challenging.

Background

Microvascular decompression (MVD) is the primary treatment for cranial neurovascular compression syndromes, such as trigeminal neuralgia (TN), hemifacial spasm (HFS), and glossopharyngeal neuralgia (GN). The surgical safety for conditions such as intracranial hemorrhage and infection has been verified. Even advanced age is no longer an absolute contraindication for surgery (1). Although MVD is associated with low morbidity and mortality, severe complications can arise. The most life-threatening of these is intraoperative and postoperative hemorrhage (26). Most postoperative intracranial hemorrhages occur infratentorially, with remote hemorrhages being rare (2, 4, 68). Intraoperative supratentorial subdural hematomas (SDH) are even less common. A recent report detailed three cases of supratentorial SDH during MVD (9). Furthermore, Wang et al. reported two cases of SDH that occurred during endoscopic MVD in patients with hemifacial spasm, and they hypothesized that this could be linked to excessive cerebrospinal fluid drainage and positioning during the procedure, though no objective evidence supports this claim (10). A retrospective study found that the biological glue suspension method is more effective in relieving postoperative symptoms compared to traditional decompression techniques, despite an increased risk of postoperative hemorrhage (11). We describe a case of acute brain swelling caused by intraoperative supratentorial SDH during MVD for trigeminal neuralgia, a scenario not previously documented in the literature.

Case presentation

A retrospective review of 480 patients who underwent MVD for hemifacial spasm, trigeminal neuralgia, or glossopharyngeal neuralgia at our hospital from February 2008 to March 2019 identified one instance of acute brain swelling due to supratentorial subdural hematoma. This case involved a 60-year-old woman with a five-year history of trigeminal neuralgia and no hypertension, coagulopathy, or systemic diseases. During surgery, she was positioned laterally, and the arachnoid membrane was routinely opened. Cerebrospinal fluid (CSF) drained slowly, causing slight cerebellar collapse. Ten minutes after dura entry, the cerebellopontine cistern was opened, leading to a sudden CSF gush and almost immediate acute brain swelling, filling the surgical field within 10 s (Supplementary Video S1). Throughout, the patient's head position remained unchanged, blood pressure and heart rate were stable, anesthesia was maintained, and the procedure followed standard protocols without any unusual circumstances. The cause of the brain swelling was unclear, given normal manipulation, unobstructed airway, and absence of surgical bleeding. We had to manage the brain swelling while considering the possibility of remote hemorrhage. Mannitol (250 ml ivgtt) and dexamethasone (10 mg i.v.) were administered to lower intracranial pressure (ICP), while cerebrospinal fluid was gradually drained from the compact subdural space. The surgical field was restored within 40 min, and ICP gradually decreased. Despite the surgical field being narrower than initially, and elevated ICP detected under the suction device, we proceeded with supracerebellar artery decompression of the trigeminal nerve in a confined space (Supplementary Video S2). Bilateral pupil monitoring during surgery showed normal results. A postoperative CT scan immediately revealed contralateral acute supratentorial subdural hematoma (SDH) with a midline shift of approximately 4 mm (Figure 1). The patient awoke from anesthesia with a Glasgow score of 15, and no obvious signs of neurological dysfunction were observed. Moreover, within 8 h after the operation, three head CT scans were completed, confirming that the volume of the subdural hematoma remained stable and did not increase further. At the same time, the patient's clinical symptoms were stable, with no obvious symptoms of increased intracranial pressure such as headache or projectile vomiting. Therefore, we did not place an ICP probe for continuous monitoring of intracranial pressure, but continued to observe the clinical symptoms and signs. Fortunately, when the CT was rechecked 21 h after the operation, it was found that most of the subdural hematoma had dissipated (Figures 2A,B). The patient was discharged eight days later without neurological impairments.

Figure 1
Four-panel image of CT brain scans labeled A, B, C, and D. Panel A shows a transverse section with sinus involvement. Panel B shows a cross-section with brain matter visible. Panel C displays another transverse section highlighting cranial structures. Panel D shows a cross-section focusing on the brain's central area.

Figure 1. Postoperative CT scan. A,B: CT at 0 h post-operation showed that there was no hemorrhage in the operation area of left cerebellopontine angle, but there was right supratentorial subdural hematoma (1 cm thickness). C,D: CT at 4 h post-operation showed that hematoma was stable.

Figure 2
CT scan showing two different brain images. Image A displays a horizontal cross-section of the brain, highlighting asymmetrical features. Image B presents a more symmetrical brain structure with clear differentiation between the gray and white matter.

Figure 2. (A,B) CT at 21 h post-operation showed that the right subdural hematoma was significantly dissipated.

Discussion

Postoperative intracranial hemorrhage remains the most common complication of posterior fossa surgery, including microvascular decompression, leading to severe consequences (12, 13). Supratentorial hemorrhage following MVD is relatively uncommon and there are only a few reports available (Supplementary Table S1). Recent literature has documented four cases of supratentorial subdural hematoma (SDH) after MVD (6) and three cases of supratentorial SDH during MVD (9). Several reports have described the clinical details of the complications (2, 6, 9). The three cases of intraoperative SDH all revealed bleeding of unknown origin within the surgical field (9). In the case of Amagasaki et al, all three HFS patients experienced bleeding in the surgical area (or continuous bloody cerebrospinal fluid) during the operation. These symptoms suggested to the surgeons that there was bleeding in the brain. In our case of TN, no bloody cerebrospinal fluid or bleeding in the surgical area was observed, but there was a transient cerebrospinal fluid overflow, which caused confusion in our judgment during the operation. Moreover, acute brain swelling followed immediately in our case, which brought greater difficulties to the surgery. In the case of Amagasaki's team, one patient underwent a second operation (to remove the subdural hematoma) and suffered from the sequelae of Gerstmann's syndrome and epilepsy. Fortunately, in this case, the subdural hematoma of the patient quickly dissipated and the neurological function was intact (9). Literature primarily discusses intraoperative bloody cerebrospinal fluid or operative site bleeding, as well as remote subdural hematomas identified during routine postoperative evaluations. In our case, no operative site bleeding was observed; however, significant brain swelling occurred, following a brief cerebrospinal fluid outflow. We propose that transient cerebrospinal fluid efflux and unexplained intraoperative brain swelling may indicate subdural hematoma at remote locations, warranting attention. The choice of hemostatic method during surgery depends on the surgical phase and the specific anatomical site of bleeding. Surgeons must be familiar with various hemostatic techniques to effectively manage bleeding, particularly in complex cranial neurosurgical cases (14). Novel hemostatic agents are utilized to manage intraoperative bleeding. The use of autologous fibrin sealant has been effective in controlling cerebral bleeding and promptly sealing the dura, leading to the resolution of cerebrospinal fluid leaks (15). IEIK13 demonstrates efficacy and safety in managing oozing hemorrhage in intracranial neurosurgical procedures. This trial supports the utility of the transparent IEIK13 hydrogel as a valuable tool for achieving hemostasis in neurosurgery (16). Among our 480 patients who underwent microvascular decompression for hemifacial spasm, trigeminal neuralgia, and glossopharyngeal neuralgia, three developed SDH. These hematomas were minor and caused no neurological deficits. While acute brain swelling from intraoperative supratentorial SDH during MVD is exceedingly rare and perilous, we found no comparable cases in the literature.

The cause of supratentorial subdural hematoma (SDH) during posterior fossa surgery remains uncertain. However, potential mechanisms include excessive cerebrospinal fluid (CSF) drainage and neck rotation and flexion in the lateral decubitus position (2, 4). Nozaki reported that transitioning patients from the intraoperative lateral position to the postoperative supine position resulted in low intracranial pressure and/or intracranial air, causing the brain to shift and subsequently leading to supratentorial subdural hematoma (6). This hypothesis fails to account for intraoperative bleeding. Recent studies indicate that most subdural hematomas occur on the nondominant side of venous drainage; however, no definitive link exists between venous drainage laterality and bleeding (6, 9). In our case, both the rate and volume of CSF drainage were normal, as previously noted. However, CSF unexpectedly surged from the cistern, which we attributed to increased ICP from the supratentorial SDH, rather than as a cause of it. The hematoma was located on the dominant side of venous drainage (Figure 3), but the relationship between supratentorial SDH and venous pressure remains unclear. Avoiding this rare complication is nearly impossible due to its unknown etiology, and a sudden intraoperative rise in CSF outflow might indicate its occurrence.

Figure 3
MRI scan showing cerebral blood vessels with a focus on the right side. Vessels are highlighted against a darker background, indicating the flow of blood in the brain.

Figure 3. Magnetic resonance venography showed that the left transverse sinus and sigmoid sinus were not visualized, and the venous drainage was mainly on the right side.

Acute brain edema is commonly seen in superior cerebral edema after trauma or obstructive hydrocephalus, leading to trans-tentorial brain hernia and requiring urgent treatment. Secondary direct temporal lobe disengagement in traumatic brain injury may offer an approach to managing trans-tentorial brain herniation, potentially avoiding more complex interventions. Encouraging clinical outcomes suggest that this method could positively impact patients' neurological recovery (17). Otherwise, Cerebellum edema, along with obstructive hydrocephalus, is an uncommon manifestation of hypertensive encephalopathy. The authors describe a unique instance of isolated swelling in the posterior fossa, leading to upward trans-tentorial herniation and subsequent hydrocephalus, resulting in neurological decline (18). In such instances, intraoperative ultrasound provides real-time imaging of structures within the surgical field, aiding surgeons in aligning intraoperative anatomical images. Intraoperative ultrasound proves to be a versatile tool in surgery, as it aids in identifying CSF and blood flow, assessing tissue characteristics, detecting peripheral infiltration, and promptly visualizing complications such as hematomas (19). Residual bleeding or hematoma during the operation is an important cause of brain edema. Visible near-infrared spectroscopic (VNIRS) is a non-invasive real-time intraoperative monitoring technology that has been applied in neurosurgery (20). It provides a reliable and convenient way for surgeons to detect and locate hematomas during the operation (21).

Acute brain swelling due to intraoperative supratentorial SDH presents a complex and hazardous challenge, necessitating urgent intervention. Determining the cause and severity of this swelling remains uncertain for surgeons, complicating decision-making. Despite the lack of a standardized approach, certain principles are essential. First, controlling brain swelling is crucial to prevent acute encephalocele, which can lead to severe, irreversible outcomes. The most effective strategy is the gradual release of CSF, requiring patience and precision to avoid brain tissue damage. Second, if abnormal pupils are detected or imaging reveals a significant remote hematoma, immediate skull closure and rapid hematoma evacuation may be imperative. In this case, the surgeon successfully managed the brain swelling, allowing for the completion of the MVD, and the hematoma resolved spontaneously by the second postoperative day.

Conclusion

Learning Points: Vigilance during sudden CSF gush, gradual drainage, importance of immediate imaging.

Surgeons must remain vigilant for intraoperative supratentorial SDH during MVD, despite its rarity, as it can result in fatal acute brain swelling and encephalocele. Preventing and managing this severe complication remains challenging.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

Ethics statement

The studies involving humans were approved by The Regional Ethics Committee of the Third Affiliated Hospital of Soochow University. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

Author contributions

JS: Writing – review & editing, Writing – original draft. JC: Data curation, Writing – review & editing. QZ: Writing – review & editing.

Funding

The author(s) declare that financial support was received for the research and/or publication of this article. Changzhou Sci & Tech Program (CJ20245009).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declare that no Generative AI was used in the creation of this manuscript.

Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fsurg.2025.1643743/full#supplementary-material

References

1. Sun J, Wang M, Zhang L, Yu Y. A meta-analysis of the effectiveness and safety of microvascular decompression in elderly patients with trigeminal neuralgia. J Clin Neurosci. (2022) 99:22–34. (In eng). doi: 10.1016/j.jocn.2022.01.020

PubMed Abstract | Crossref Full Text | Google Scholar

2. Hanakita J, Kondo A. Serious complications of microvascular decompression operations for trigeminal neuralgia and hemifacial spasm. Neurosurgery. (1988) 22(2):348–52. (In eng). doi: 10.1227/00006123-198802000-00012

PubMed Abstract | Crossref Full Text | Google Scholar

3. Kalkanis SN, Eskandar EN, Carter BS, Barker FG 2nd. Microvascular decompression surgery in the United States, 1996 to 2000: mortality rates, morbidity rates, and the effects of hospital and surgeon volumes. Neurosurgery. (2003) 52(6):1251–61. discussion 1261-2. (In eng). doi: 10.1227/01.neu.0000065129.25359.ee

PubMed Abstract | Crossref Full Text | Google Scholar

4. Li N, Zhao W, Pu C, Shen J. Delayed hemorrhage following microvascular decompression. Three case reports. Neurol Med Chir (Tokyo). (2007) 47(4):186–8. (In eng). doi: 10.2176/nmc.47.186

PubMed Abstract | Crossref Full Text | Google Scholar

5. McLaughlin MR, Jannetta PJ, Clyde BL, Subach BR, Comey CH, Resnick DK. Microvascular decompression of cranial nerves: lessons learned after 4400 operations. J Neurosurg. (1999) 90(1):1–8. (In eng). doi: 10.3171/jns.1999.90.1.0001

PubMed Abstract | Crossref Full Text | Google Scholar

6. Nozaki T, Sugiyama K, Sameshima T, Kawaji H, Namba H. Supratentorial subdural hematoma following microvascular decompression: a report of four cases. SpringerPlus. (2016) 5:353. (In eng). doi: 10.1186/s40064-016-2002-2

PubMed Abstract | Crossref Full Text | Google Scholar

7. Barker FG 2nd, Jannetta PJ, Bissonette DJ, Larkins MV, Jho HD. The long-term outcome of microvascular decompression for trigeminal neuralgia. N Engl J Med. (1996) 334(17):1077–83. (In eng). doi: 10.1056/nejm199604253341701

PubMed Abstract | Crossref Full Text | Google Scholar

8. Oh IH, Choi SK, Park BJ, Kim TS, Rhee BA, Lim YJ. The treatment outcome of elderly patients with idiopathic trigeminal neuralgia: micro-vascular decompression versus gamma knife radiosurgery. J Korean Neurosurg Soc. (2008) 44(4):199–204. (In eng). doi: 10.3340/jkns.2008.44.4.199

PubMed Abstract | Crossref Full Text | Google Scholar

9. Amagasaki K, Takusagawa Y, Kanehashi K, Abe S, Watanabe S, Shono N, et al. Supratentorial acute subdural haematoma during microvascular decompression surgery: report of three cases. J Surg Case Rep. (2017) 2017(2):rjx004. (In eng). doi: 10.1093/jscr/rjx004

PubMed Abstract | Crossref Full Text | Google Scholar

10. Wang J, Wang X, Luo T, Wang X, Qu Y. Supratentorial acute subdural hematoma during fully endoscopic microvascular decompression surgery for hemifacial spasm. J Craniofac Surg. (2023) 34(2):e187–90. (In eng). doi: 10.1097/scs.0000000000008987

PubMed Abstract | Crossref Full Text | Google Scholar

11. Liu J, Shen Y, Xiayizhati K, Yuik Y. Postoperative hemorrhage after biomedical glue sling technique in microvascular decompression for vertebrobasilar artery-associated cranial nerve diseases: a retrospective study of 14 cases. Front Surg. (2022) 9:943848. (In eng). doi: 10.3389/fsurg.2022.943848

PubMed Abstract | Crossref Full Text | Google Scholar

12. Friedman JA, Piepgras DG, Duke DA, McClelland RL, Bechtle PS, Maher CO, et al. Remote cerebellar hemorrhage after supratentorial surgery. Neurosurgery. (2001) 49(6):1327–40. (In eng). doi: 10.1097/00006123-200112000-00008

PubMed Abstract | Crossref Full Text | Google Scholar

13. Dubey A, Sung WS, Shaya M, Patwardhan R, Willis B, Smith D, et al. Complications of posterior cranial fossa surgery–an institutional experience of 500 patients. Surg Neurol. (2009) 72(4):369–75. (In eng). doi: 10.1016/j.surneu.2009.04.001

PubMed Abstract | Crossref Full Text | Google Scholar

14. Delawan M, Sharma M, Ismail M, Algabri MH, Abdalridha RH, Alawadi MN, et al. Methods of hemostasis in cranial neurosurgery: an anatomy-based stepwise review. World Neurosurg. (2023) 178:241–259.e3. (In eng). doi: 10.1016/j.wneu.2023.08.030

PubMed Abstract | Crossref Full Text | Google Scholar

15. Graziano F, Certo F, Basile L, Maugeri R, Grasso G, Meccio F, et al. Autologous fibrin sealant (vivostat(®)) in the neurosurgical practice: part I: intracranial surgical procedure. Surg Neurol Int. (2015) 6:77. (In eng). doi: 10.4103/2152-7806.156871

PubMed Abstract | Crossref Full Text | Google Scholar

16. Verbraeken B, Plazier M, Put E, Meeuws S, Roosen G, Ughratdar I, et al. Self-Assembling peptide IEIK13 for intraoperative hemostasis in cranial neurosurgery: clinical trial on efficacy and safety. World Neurosurg. (2025) 197:123856. (In eng). doi: 10.1016/j.wneu.2025.123856

PubMed Abstract | Crossref Full Text | Google Scholar

17. Scibilia A, Gallinaro P, Todeschi J, Chibbaro S, Dannhoff G, Ollivier I, et al. Surgical management of persistent post-traumatic trans-tentorial brain hernia. Neurochirurgie. (2022) 68(1):44–51. (In eng). doi: 10.1016/j.neuchi.2021.06.012

PubMed Abstract | Crossref Full Text | Google Scholar

18. Adamson DC, Dimitrov DF, Bronec PR. Upward transtentorial herniation, hydrocephalus, and cerebellar edema in hypertensive encephalopathy. Neurologist. (2005) 11(3):171–5. (In eng). doi: 10.1097/01.nrl.0000159982.63592.9f

PubMed Abstract | Crossref Full Text | Google Scholar

19. Ganau M, Ligarotti GK, Apostolopoulos V. Real-time intraoperative ultrasound in brain surgery: neuronavigation and use of contrast-enhanced image fusion. Quant Imaging Med Surg. (2019) 9(3):350–8. (In eng). doi: 10.21037/qims.2019.03.06

PubMed Abstract | Crossref Full Text | Google Scholar

20. Dilmen OK, Akcil EF, Vehid H, Tunali Y. Cerebral oxygenation assessed by near-infrared spectroscopy in the sitting and prone positions during posterior fossa surgery: a prospective, randomized clinical study. Braz J Anesthesiol. (2023) 73(5):589–94. (In eng). doi: 10.1016/j.bjane.2021.09.016

PubMed Abstract | Crossref Full Text | Google Scholar

21. Chen M, Liu Y, Dang Y, Wang H, Wang N, Chen B, et al. Application research of visible near-infrared spectroscopy technology for detecting intracerebral hematoma. World Neurosurg. (2023) 180:e422–8. (In eng). doi: 10.1016/j.wneu.2023.09.082

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: microvascular decompression, trigeminal neuralgia, subdural hematoma, encephalocele - complications, complication

Citation: Shi J, Cao J and Zhou Q (2025) Acute brain swelling due to intraoperative supratentorial subdural hematoma during microvascular decompression: a case report. Front. Surg. 12:1643743. doi: 10.3389/fsurg.2025.1643743

Received: 9 June 2025; Accepted: 6 October 2025;
Published: 24 October 2025.

Edited by:

Sunil Manjila, Insight Institute of Neurosurgery and Neuroscience (IINN), United States

Reviewed by:

Luis Rafael Moscote-Salazar, Colombian Clinical Research Group in Neurocritical Care, Colombia
Zhiqin Lin, Fujian Medical University, China
Darpanarayan Hazra, Sultan Qaboos University, Oman

Copyright: © 2025 Shi, Cao and Zhou. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Qiang Zhou, emhvdXFpYW5nNTA3QDEyNi5jb20=

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.