Skip to main content
Frontiers in Surgery logoLink to Frontiers in Surgery
. 2026 Oct 19;13:1882255. doi: 10.3389/fsurg.2026.1882255

Recurrent postoperative symptomatic epidural hematoma after thoracic decompression surgery: a case report and literature review

Xuyu Liao 1,*, Liujun Zhao 1, Yong Hu 1, Liang Yu 1, Yunlin Chen 1, Xudong Hu 1, Weihu Zhang 1
PMCID: PMC13724321  PMID: 42973451

Abstract

Background

Postoperative symptomatic epidural hematoma (PSEH) is a rare but potentially devastating complication following thoracic decompression surgery, with an incidence of less than 1%. While isolated PSEH has been well documented, recurrent PSEH,particularly in the thoracic spine which represents an exceptionally rare phenomenon with limited literature available to guide clinical management.

Case presentation

This is a case of a 64-year-old male patient who underwent thoracic decompression surgery for ossification of the ligamentum flavum and developed recurrent PSEH requiring two hematoma evacuations. Due to the timely removing the collagenase covering the dural surface and meticulous intraoperative hemostasis, excellent clinical outcomes were achieved in the end.

Conclusion

Recurrent symptomatic epidural hematoma after thoracic decompression is an exceedingly rare but serious complication. Early recognition, prompt surgical intervention, meticulous management of intraspinal venous hemorrhage and identification of underlying risk factors are essential for optimizing neurological outcomes. This case adds to the limited literature on recurrent PSEH and highlights considerations for intraoperative management.

Keywords: decompression, surgical, hematoma, epidural, spinal, postoperative complications, recurrence, thoracic vertebrae

Background

Thoracic spine decompression surgery is a common procedure for addressing conditions such as thoracic spinal stenosis caused by ossification of the ligamentum flavum (OLF), ossification of the posterior longitudinal ligament (OPLL), disc protrusion, and traumatic spinal cord compression (1, 2). While generally considered safe, the procedure carries inherent risks, including cerebrospinal fluid leakage, neurological deterioration, and postoperative symptomatic epidural hematoma (PSEH). Although rare, PSEH can be a devastating complication, potentially leading to bowel and bladder dysfunction, saddle anesthesia, motor weakness in the lower extremities, and sexual dysfunction (3). The incidence of PSEH in the thoracic spine is reported to be approximately 1.49% (4), which is notably higher than that following posterior cervical surgery (0.68%), anterior cervical discectomy and fusion (0.44%), and posterior lumbar decompression and fusion (0.10%–0.86%) (5–14).

Conventionally, during thoracic decompression surgery, careful dural handling is required to prevent dural laceration and minimise extensive disruption of the epidural venous plexus. Should bleeding occur, meticulous haemostasis is performed with bipolar electrocoagulation of the fragile, rich epidural venous plexus, combined with packing of the lateral wall of the thoracic canal using gelatin sponge. Bone bleeding is controlled with bone wax. Two negative pressure drainage tubes are routinely placed after the operation to drain the accumulated blood in the wound and prevent postoperative hematoma.

Recurrent PSEH defined as hematoma reformation at the same surgical site after initial evacuation,remains an exceptionally rare event in the literature (15, 16).Given the paucity of published data, guidance for managing such cases is limited. In this report, we describe a case of recurrent symptomatic epidural hematoma following thoracic decompression surgery in a patient with no history of hemorrhagic disease or antiplatelet medication use.

Case presentation

A 64-year-old male presented on February 1, 2025, with a two-year history of progressive numbness and weakness in both lower extremities. His symptoms had worsened over the past month, rendering him unable to walk and wheelchair-dependent. His medical history was significant for hypertension and hyperlipidemia, managed with valsartan hydrochlorothiazide and atorvastatin. Notably, he had undergone an L4/5 laminectomy at a local hospital 25 years prior. His BMI was 28.4 kg/m².

Physical examination revealed atrophy of the right calf muscle, accompanied by foot drop and clubfoot. Deep tendon reflexes were active in the left patella and hyperactive in the right. The left Babinski sign was positive, while the Hoffmann sign was negative bilaterally. A detailed summary of lower extremity muscle strength is provided in Table 1.

Table 1.

Muscle strength of lower extremity at admission.

Key Muscles Muscle Strength
Left Right
iliopsoas III III
quadriceps femoris III III
hamstring muscles III III
tibialis anterior muscle III 0
extensor digitorum longus III 0
fibular longus and brevis muscles III 0
triceps surae IV IV

Preoperative CT and MRI demonstrated spinal canal stenosis in the thoracic and lumbar regions, with the most severe compression at the T10-T11 level due to OLF (Figure 1). The patient underwent en-bloc technique for complete resection of the posterior wall of the spinal canal from T10 to L1 that includes the ossified ligamentum flavum by ultrasonic bone scalpel (Figure 2). A medical collagen membrane (GTR Fujian) was placed over the spinal dura mater to prevent adhesions.

Figure 1.

CT scan showing two views of the thoracic spine with ossification of the ligamentum flavum (OLF) indicated by arrows; axial view on the left (A) and sagittal view on the right (B).

CT revealed that the most severe OLF (ossification of the ligamentum flavum) was located in the T10∼T11 level. (A): Axial CT image demonstrates spinal canal stenosis secondary to OLF (white arrow). (B): Sagittal reformatted-CT image illustrates spinal canal compression by OLF (white arrow).

Figure 2.

Surgical specimen of a human vertebral segment is placed on a blue surgical drape. White labels and arrows indicate anatomical levels: T10-T11, T11-T12, and T12-L1.

The posterior wall of the spinal canal from T10 to L1 that includes the ossified ligamentum flavum was en bloc resected.

Six hours postoperatively, the patient’s iliopsoas and quadriceps muscle strength had recovered to grade IV. However, 13 h after the initial surgery, he reported new-onset numbness in both lower extremities. Muscle strength in the bilateral iliopsoas and quadriceps had deteriorated to grade I, and the left tibialis anterior, fibularis longus, and extensor hallucis longus muscles were also grade I. A diagnosis of PSEH was made. After obtaining informed consent, an emergent hematoma evacuation was performed. Intraoperatively, the collagen membrane was removed, revealing a small amount of clotted blood on the dural surface. Despite irrigation with iced saline, persistent oozing was noted from the venous plexus on the lateral wall of the spinal canal. Four negative-pressure drains were subsequently placed. Six hours after this second surgery, the strength in his bilateral iliopsoas and quadriceps had again improved to grade IV. Tragically, 10 h later, his condition worsened once more, with the same muscles weakening to grade I. An emergent MRI confirmed a recurrent epidural hematoma at the surgical site (Figure 3), necessitating a third operation for evacuation.

Figure 3.

MRI showing two spinal views labeled as A and B; both highlight a hematoma indicated by white arrows, with A showing a sagittal view and B showing an axial view of the spine.

MRI shows an epidural hematoma at the surgical site with compression of the dural sac (white arrow). (A): The sagittal MRI image shows that the dural sac is compressed and flattened. (B): The axial MRI image shows that the dural sac is compressed and flattened.

During this third procedure, the incision was found to be filled with blood clots (Figure 4). Following clot removal, meticulous hemostasis was achieved using bipolar electrocoagulation. A fluid gelatin was applied to fill the lateral wall of the spinal canal, and four large-diameter drainage tubes were placed to prevent further accumulation. Twenty-four hours after this final surgery, the patient’s bilateral iliopsoas and quadriceps strength had recovered to grade III.

Figure 4.

Surgical site exposing deep tissue and muscle layers with visible blood and retracted skin, showing an open wound held apart by metal retractors on either side.

The surgical incision was filled with blood clots.

He was discharged on February 21, 2025, at which point his right foot drop had partially improved, and he was able to walk for 10 min with a walking aid (see Table 2 for a full muscle strength assessment). At a one-month follow-up, his strength had improved further, allowing him to walk 30 steps without crutches. Fourteen months post-discharge, he was able to walk freely and independently for 20 min.

Table 2.

Muscle strength of lower extrimity at discharge.

Key Muscles Muscle Strength
Left Right
iliopsoas IV IV
quadriceps femoris IV IV
hamstring muscles IV IV
tibialis anterior muscle IV III
extensor digitorum longus IV II
fibular longus and brevis muscles IV 0
triceps surae IV IV

Discussion

The present case demonstrates that PSEH can occur repeatedly, presenting as a serious complication that causes neurologic impairment, including lower extremity paralysis, and saddle anesthesia. Bowel and bladder dysfunction may also result, though this is less commonly observed in the thoracic spine (17).

Current research suggests that the physiological kyphosis of the thoracic spine narrows the space between the paravertebral muscles and the spinal cord when a small hematoma is present. This anatomical compression is believed to explain why PSEH occurs more frequently in the thoracic region than in the cervical or lumbar spine (18, 19). Another contributing factor may be regional differences in spinal cord blood flow. Marcus et al. reported that average blood flow in the cervical and lumbosacral segments is approximately 40% higher than in the thoracic spinal cord (20), potentially making the thoracic segment more vulnerable to ischemic injury following compression.

Anatomically, the epidural venous plexus is an unvalved vascular network with thin and fragile walls that can easily dilate under compression (21, 22). A high occupancy ratio due to thoracic spinal stenosis reduces the elasticity of the epidural venous plexus and impedes blood flow, predisposing it to bleeding. Once hemorrhage occurs, spontaneous hemostasis is difficult to achieve. Consequently, dilatation of the epidural venous plexus contributes to the development of epidural hematoma (23, 24). Therefore, for patients with a high occupancy rate, meticulous surgical technique and rigorous control of venous plexus bleeding are of paramount importance.

Recurrent PSEH defined as hematoma reformation at the same surgical site following initial evacuation that is exceptionally rare. A PubMed review of the English-language literature using the terms “spinal epidural hematoma” and “recurrent” or “relapsed” yielded only seven reported articles documenting recurrent PSEH (Table 3). Given its rarity and potential to cause severe neurological sequelae, recurrent PSEH warrants aggressive treatment (31).

Table 3.

Patients with recurrence spinal epidural hematoma.

Reference N Author/year Age(y)/sex Procedure Location IT to the 1st OP/procedure IT to the 2st OP/procedure IT to the 3rd OP/procedure IT to the 4th OP/procedure IT to the 5th OP/procedure Symptom Primary cause Outcome
1 Liao/2009 (25) 8/F evacuation of SSEH C3–T8 6 years/evacuation of C2-C4 incomplete tetraplegia (ASIA Grade C) vascular malformation ICR
41/M evacuation of SSEH L1-5 48 h/ESD bach pain and weakness in both legs Child Class C cirrhosis and preoperative coagulopathy ICR
53/M evacuation of SSEH  T4–L3 15 h/ESD complete paraplegia ESRD ICR
2 Lim/2011 (26) 57/M hemilaminectomy and hematoma evacuation T11-L3 1 day/total laminectomy(T11-L4) and ESD low back pain and weakness of the left lower limb clopidogrel and aspirin ICR
3 Hernandez D/1982 (27) 67/M anterior corpectomy and fusion C6-7 20 days/posterior decompressive laminectomy 17 days/conservative acute motor deficit Dual antiplatelet therapy ICR
4 Anno/2015 (28) 71/M posterior decompression C4-5 6 h/ ESD 2 h/ ESD tetraplegia Protein S Deficiency CR
5 Luo/2016 (16) 34/M posterior laminectomy and hematoma evacuation L3-4 8 days/NPWT leg numbness and weakness hemophilia A CR
6 Kenneth C/2017 (29) 72/F posterior decompression L2-4 2 days/ ESD 1 h/NPDT back pain and leg pain and leg paraplegia Dual antiplatelet therapy ICR
72/F posterior fusion C2-T1 8 days/ ESD 2 days/NPDT weakness and sensory deficit in the bilateral upper extremities a baseline coagulopathy secondary to cirrhosis ICR
81/M posterior fusion C3-4 17 days/ ESD anesthesia recovery/NPDT  severe neck pain and tetraplegia pulmonary embolism and deep venous thrombosis ICR
7 Mohammed M/2019 (30) 24/M posterior decompression L3-4 3 days/ evacuation 2 days/ evacuation 28 days/ evacuation 1 day/ evacuation 1day/ evacuation  weakness in both legs and incontinence Glanzmann thrombasthenia CR

M, male; F, female; OP, operation; IT, interval time; ESD, evacuation and suction drain; NPDT, negative-pressure dressing therapy; NPWT, negative-pressure wound therapy; CR, complete recovery; ICR, incomplete recovery; ESRD, end-stage renal disease; SSEH, spontaneous spinal epidural hematoma.

Based on our experience with the present case, we believe the following points merit attention when managing PSEH:

Dural Covering Materials as High Risk Factors: Covering substances placed on the dura mater, such as gelatin sponges or collagen membranes, may increase the risk of epidural hematoma formation. These materials can become saturated with blood and surrounded by clot, potentially exerting a mass effect for up to three days postoperatively (32).

Hemostasis of the Intraspinal Venous Plexus: Hemorrhage from the intraspinal venous plexus in the thoracic canal must be actively controlled using bipolar electrocoagulation. If necessary, lateral extension of the decompression may improve exposure of the venous plexus on the ventral aspect of the dura. When bipolar electrocoagulation alone is insufficient, application of liquid gelatin hemostatic agent can be beneficial. In our case, during the second hematoma evacuation, hemostasis was achieved through bipolar electrocoagulation followed by uniform application of liquid gelatin to the expanded lateral wall of the thoracic spinal canal, which yielded excellent hemostatic effect.

Hemostasis Versus Drainage: Effective hemostasis is far more critical than multiple drains. During the first evacuation in this case, failure to achieve adequate hemostasis resulted in hematoma recurrence despite placement of four negative-pressure drains—when the rate of bleeding exceeds the rate of drainage, hematoma re-accumulation is inevitable.

Role of Coagulation Support: Postoperative administration of small, repeated doses of fresh frozen plasma may improve coagulation function and facilitate hemostasis at the surgical site, particularly in patients who have undergone multiple procedures.

In the present case, the collagen membrane contributed to the initial PSEH, whereas hemorrhage from the intraspinal venous plexus was the primary driver of recurrence. Surgeons should remain vigilant to the possibility of PSEH recurrence, particularly in patients undergoing posterior thoracic surgery, and should recognize that dural covering materials, high BMI, hypertension, and hyperlipidemia are potential risk factors for this complication.

Conclusion

Recurrent symptomatic epidural hematoma is an extremely rare yet severe complication following thoracic decompression. Optimized clinical outcomes rely on early recognition, prompt surgical intervention, meticulous hemostasis of intraspinal venous bleeding, aggressive postoperative supportive care, and identification of underlying risk factors.

Funding Statement

The author(s) declared that financial support was received for this work and/or its publication. Funded by Ningbo Clinical Research Center for Orthopedics, Sports Medicine & Rehabilitation (2024L004).

Footnotes

Edited by: Philipp Taussky, Beth Israel Deaconess Medical Center and Harvard Medical School, United States

Reviewed by: Riyadh Firdaus, University of Indonesia, Indonesia

Luis Garcia Rairan, National University of Colombia, Colombia

Abbreviations CT, computed tomography; MRI, magnetic resonance imaging; PSEH, postoperative symptomatic epidural hematoma; OLF, ossification of the ligamentum flavum; OPLL, ossification of the posterior longitudinal ligament.

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 Ethics Committee of the Ningbo NO.6 hospital [2026(L)011]. 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

XL: Writing – original draft, Writing – review & editing, Supervision, Funding acquisition, Data curation. LZ: Software, Writing – review & editing, Validation, Data curation. YH: Project administration, Software, Supervision, Resources, Formal analysis, Writing – review & editing. LY: Supervision, Data curation, Methodology, Writing – review & editing, Validation. YC: Software, Data curation, Formal analysis, Writing – review & editing. XH: Resources, Writing – review & editing, Data curation, Supervision. WZ: Formal analysis, Methodology, Investigation, Software, Writing – review & editing.

Conflict of interest

The author(s) declared that this work 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) declared that generative AI was not 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.

References

  • 1.Maruyama J, Furuya T, Maki S, Inoue T, Yunde A, Miura M, et al. Posterior decompression and fixation for thoracic spine ossification: a 10-year follow-up study. J Clin Med. (2023) 12(17):5701. 10.3390/jcm12175701 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Ito S, Nakashima H, Segi N, Ouchida J, Oishi R, Yamauchi I, et al. Ten-year follow-up of posterior decompression and fusion surgery for thoracic ossification of the posterior longitudinal ligament. J Bone Joint Surg Am. (2024) 106(17):1600–9. 10.2106/JBJS.23.01475 [DOI] [PubMed] [Google Scholar]
  • 3.Knusel K, Du JY, Ren B, Kim CY, Ahn UM, Ahn NU. Symptomatic epidural hematoma after elective posterior lumbar decompression: incidence, timing, risk factors, and associated complications. HSS J. (2020) 16(Suppl 2):230–7. 10.1007/s11420-019-09690-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Wang L, Wang H, Sun Z, Chen Z, Sun C, Li W. Incidence and risk factors for symptomatic spinal epidural hematoma following posterior thoracic spinal surgery in a single institute. Global Spine J. (2022) 12(6):1175–83. 10.1177/2192568220979141 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Pivazyan G, Kim AJ, Aguilera CJ, Khan Z, Bryant JP, Stewart JJ, et al. Incidence, risk factors, and functional outcomes of symptomatic postoperative spinal epidural hematoma: a case-control study. World Neurosurg. (2025) 193:851–60. 10.1016/j.wneu.2024.10.070 [DOI] [PubMed] [Google Scholar]
  • 6.Aikeremu A, Liu G. Risk factors of postoperative spinal epidural hematoma after transforaminal lumbar interbody fusion surgery. Neurochirurgie. (2021) 67(5):439–44. 10.1016/j.neuchi.2021.04.012 [DOI] [PubMed] [Google Scholar]
  • 7.Butler AJ, Donnally CJ, 3rd, Goz V, Basques BA, Vaccaro AR, Schroeder GD. Symptomatic postoperative epidural hematoma in the lumbar spine. Clin Spine Surg. (2022) 35(9):354–62. 10.1097/BSD.0000000000001278 [DOI] [PubMed] [Google Scholar]
  • 8.Goldstein CL, Bains I, Hurlbert RJ. Symptomatic spinal epidural hematoma after posterior cervical surgery: incidence and risk factors. Spine J. (2015) 15:1179–87. 10.1016/j.spinee.2013.11.043 [DOI] [PubMed] [Google Scholar]
  • 9.Djurasovic M, Campion C, Dimar JR, 2nd, Glassman SD, Gum JL. Postoperative epidural hematoma. Orthop Clin North Am. (2022) 53(1):113–21. 10.1016/j.ocl.2021.08.006 [DOI] [PubMed] [Google Scholar]
  • 10.Tian Y, Han Y, Li J, Wang M, Qu Y, Fang J, et al. Incidence and risk factors of postoperative epidural hematoma following anterior cervical spine surgery. Beijing Da Xue Xue Bao Yi Xue Ban. (2024) 56(6):1058–64. 10.19723/j.issn.1671-167X.2024.06.018 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Hohenberger C, Zeman F, Höhne J, Ullrich O-W, Brawanski A, Schebesch K-M. Symptomatic postoperative spinal epidural hematoma after spinal decompression surgery: prevalence, risk factors, and functional outcome. J NeurolSurg A Cent Eur Neurosurg. (2020) 81:290–6. 10.1055/s-0039-1697024 [DOI] [PubMed] [Google Scholar]
  • 12.Kao F-C, Tsai T-T, Chen L-H, Lai P-L, Fu T-S, Niu C-C, et al. Symptomatic epidural hematoma after lumbar decompression surgery. Eur Spine J. (2015) 24:348–57. 10.1007/s00586-014-3297-8 [DOI] [PubMed] [Google Scholar]
  • 13.Yin G, Ni B. Acute postoperative cervical spinal epidural hematoma. Acta Orthop Traumatol Turc. (2014) 48:437–42. 10.3944/AOTT.2014.13.0133 [DOI] [PubMed] [Google Scholar]
  • 14.Liao Y, Tian Y, Ye R, Tang C, Tang Q, Ma F, et al. Risk and treatment of symptomatic epidural hematoma after anterior cervical spine surgery. Medicine (Baltimore). (2020) 99:e18711. 10.1097/MD.0000000000018711 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Morimoto D, Kim K, Kubota A, Kokubo R, Iwamoto N, Hattori Y, et al. Recurrent cervical spinal epidural hematoma: case report and literature review. NMC Case Rep J. (2020) 7(4):157–60. 10.2176/nmccrj.cr.2019-0253 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Luo XB, Zhou X, Wang Q, Cai XJ, Luo ZP, Ma YZ. The classification of recurrent spinal epidural hematoma: a review of the literature and a comparison with the cases. Eur Spine J. (2016 May) 25(Suppl 1):224–9. 10.1007/s00586-016-4506-4 [DOI] [PubMed] [Google Scholar]
  • 17.Liu J-M, Deng H-L, Zhou Y, Chen X-Y, Yang D, Duan M-S, et al. Incidence and risk factors for symptomatic spinal epidural haematoma following lumbar spinal surgery. Int Orthop. (2017) 41:2297–302. 10.1007/s00264-017-3619-7 [DOI] [PubMed] [Google Scholar]
  • 18.Amiri AR, Fouyas IP, Cro S, Casey AT. Postoperative spinal epidural hematoma (SEH): incidence, risk factors, onset, and management. Spine J. (2013) 13(2):134–40. 10.1016/j.spinee.2012.10.028 [DOI] [PubMed] [Google Scholar]
  • 19.Aono H, Ohwada T, Hosono N, Tobimatsu H, Ariga K, Fuji T, et al. Incidence of postoperative symptomatic epidural hematoma in spinal decompression surgery. J Neurosurg Spine. (2011) 15(2):202–5. 10.3171/2011.3.SPINE10716 [DOI] [PubMed] [Google Scholar]
  • 20.Marcus ML, Heistad DD, Ehrhardt JC, Abboud FM. Regulation of total and regional spinal cord blood flow. Circ Res. (1977) 41(1):128–34. 10.1161/01.RES.41.1.128 [DOI] [PubMed] [Google Scholar]
  • 21.Morikawa M, Sato S, Numaguchi Y, Mihara F, Rothman MI. Spinal epidural venous plexus: its MR enhancement patterns and their clinical significance. Radiat Med. (1996) 14(5):221–7. [PubMed] [Google Scholar]
  • 22.Paksoy Y, Gormus N. Epidural venous plexus enlargements presenting with radiculopathy and back pain in patients with inferior vena cava obstruction or occlusion. Spine (Phila Pa 1976). (2004) 29(21):2419–24. 10.1097/01.brs.0000144354.36449.2f [DOI] [PubMed] [Google Scholar]
  • 23.Kou J, Fischgrund J, Biddinger A, Herkowitz H. Risk factors for spinal epidural hematoma after spinal surgery. Spine (Phila Pa 1976). (2002) 27(15):1670–3. 10.1097/00007632-200208010-00016 [DOI] [PubMed] [Google Scholar]
  • 24.Groen RJ, Ponssen H. The spontaneous spinal epidural hematoma A study of the etiology. J Neurol Sci. (1990) 98(2-3):121–38. 10.1016/0022-510X(90)90253-J [DOI] [PubMed] [Google Scholar]
  • 25.Liao C-C, Hsieh P-C, Lin T-K, Lin C-L, Lo Y-L, Lee S-C. Surgical treatment of spontaneous spinal epidural hematoma: a 5-year experience. J Neurosurg Spine. (2009) 11(4):480–6. 10.3171/2009.4.SPINE08904 [DOI] [PubMed] [Google Scholar]
  • 26.Lim SH, Hong BY, Cho YR, Kim HS, Lee JI, Kim HW, et al. Relapsed spontaneous spinal epidural hematoma associated with aspirin and clopidogrel. Neurol Sci. (2011) 32(4):687–9. 10.1007/s10072-011-0508-5 [DOI] [PubMed] [Google Scholar]
  • 27.Hernandez D, Vinuela F, Feasby TE. Recurrent paraplegia with total recovery from spontaneous spinal epidural hematoma. Ann Neurol. (1982) 11(6):623–4. 10.1002/ana.410110611 [DOI] [PubMed] [Google Scholar]
  • 28.Anno M, Yamazaki T, Hara N, Hayakawa K. Recurrent postoperative spinal epidural hematoma in a patient with protein S deficiency. Case Rep Orthop. (2015) 2015:536592–3. 10.1155/2015/536592 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Foxx KC, Mesfin A, Molinari R. Negative-pressure dressing management of recurrent postoperative epidural hematoma and uncontrollable intraoperative hemorrhage in posterior spine surgery: report of 4 cases. J Neurosurg Spine. (2018) 28(2):220–5. 10.3171/2017.5.SPINE17387 [DOI] [PubMed] [Google Scholar]
  • 30.Al Barbarawi MM, Allouh MZ, Audat ZA, Aleshawi AJ, Al-Shari OM. Unique case of successful surgical treatment of recurrent spinal epidural hematoma after lumbar disc surgery in a glanzmann thrombasthenia patient. Br J Neurosurg. (2023) 37(4):853–5. 10.1080/02688697.2019.1678736 [DOI] [PubMed] [Google Scholar]
  • 31.Hans P, Delleuze PP, Born JD, Bonhomme V. Epidural hematoma after cervical spine surgery. J Neurosurg Anesthesiol. (2003) 15:282–5. 10.1097/00008506-200307000-00020 [DOI] [PubMed] [Google Scholar]
  • 32.Gao WS, Ren B, An J, Zhou XZ. Symptomatic epidural hematoma caused by absorbable gelatin sponge implantation: a case report. Asian J Surg. (2023) 46(12):6035–6. 10.1016/j.asjsur.2023.09.032 [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

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.


Articles from Frontiers in Surgery are provided here courtesy of Frontiers Media SA

RESOURCES