Biportal Endoscopic Spine Surgery for Symptomatic Postoperative Discal Pseudocyst Following Percutaneous Endoscopic Interlaminar Discectomy: A Case Report and Literature Review

Article information

J Minim Invasive Spine Surg Tech. 2025;10(1):152-161
Publication date (electronic) : 2025 April 30
doi : https://doi.org/10.21182/jmisst.2024.01753
1Department of Neurosurgery, Xuyen A General Hospital, Ho Chi Minh City, Vietnam
2Department of Neurosurgery, Nguyen Tri Phuong Hospital, Ho Chi Minh City, Vietnam
3Faculty of Medicine, University of Medicine and Pharmacy at HCMC, Ho Chi Minh City, Vietnam
Corresponding Author: Tran Vu Hoang Duong Department of Neurosurgery, Xuyen A General Hospital, 22 Street, Ho Chi Minh City, Vietnam Email: tranvuhoangduong@gmail.com
Received 2024 August 31; Revised 2024 September 27; Accepted 2024 December 23.

Abstract

Postoperative discal pseudocyst (PDP) is a rare complication after surgery for lumbar disc herniation. The literature on this condition is sparse, with most studies being limited to case reports. Various hypotheses regarding the pathogenesis of PDP have been proposed; however, the exact mechanisms remain unclear and are not well described in the current literature. We present a case of PDP following percutaneous endoscopic interlaminar discectomy (PEID), which was revised through biportal endoscopic spinal surgery. Additionally, we conducted a systematic review of the literature, aiming to provide a more detailed description of the proposed mechanisms underlying PDP, particularly after PEID, and to summarize current trends in the treatment of this complication.

INTRODUCTION

Percutaneous endoscopic interlaminar discectomy (PEID) for lumbar disc herniation (LDH) is a minimally invasive technique that has been gaining wider adoption recently [1-4]. Alongside its effectiveness, this procedure offers several advantages, such as preserving the anatomical structures of the spine and maintaining a low complication rate [3,5]. Postoperative discal pseudocyst (PDP) is an uncommon complication following PEID, with its etiology and pathogenesis still not well understood [6-9]. Most patients with PDP are asymptomatic or experience mild symptoms that can be managed conservatively [10,11]. However, some cases do not respond to conservative treatment and exhibit worsening nerve root compression symptoms, necessitating surgical intervention [8,10,12-14]. We report a case of PDP following PEID that was successfully treated with biportal endoscopic spinal surgery (BESS) technique and systematic review of the literature.

CASE REPORT

A 24-year-old male presented to our hospital with left leg pain and numbness persisting for approximately 6 months, which was unresponsive to conservative treatment and physical therapy. His pain had intensified over the past week. On examination, his hip joint range of motion was normal. The straight-leg raising test was positive on the left at 20°. Reflexes in the left knee and ankle were normal. While no abnormalities were detected in other lower extremity muscles, he struggled to walk on his left heel. The bilateral femoral nerve stretch test was negative. Skin sensation in the perineal and sellar regions was normal, and bilateral Babinski signs were negative. The visual analogue scale (VAS) score for his left leg pain was 8. Magnetic resonance imaging (MRI) revealed a left-sided disc herniation at the L4–5 level (Figure 1).

Figure 1.

Preoperative magnetic resonance imaging (MRI): left-side L4–5 disc herniation (red arrowhead). (A) Sagittal T2-weighted MRI, (B) Sagittal T1-weighted MRI, (C) Axial T2-weighted MRI.

PEID was performed, and a drainage catheter was placed over the dura mater, which was removed on the second postoperative day. Immediately after surgery, the left leg pain and numbness significantly improved, with the VAS score reducing to 2. The patient was discharged on the fifth postoperative day after a thorough examination confirmed that the surgical wound was completely dry with no signs of fluid accumulation.

However, 4 weeks postoperation, the patient returned with gradually increasing pain and paresthesia in his left leg, though less severe than before. MRI revealed a cystic lesion on the left side of the intervertebral disc at L4–5, corresponding to the site of the previous endoscopic approach, T1-weighted MRI images showed low signal intensity, while T2-weighted images showed high signal intensity (Figure 2). We diagnosed a PDP following PEID. The patient was managed with pain relief, nonsteroidal anti-inflammatory drugs (NSAIDs), and gabapentin for 4 weeks, but there was no improvement, and the left leg numbness progressively worsened. Consequently, we planned revision surgery using the BESS procedure to remove the PDP.

Figure 2.

Four-week postoperative magnetic resonance imaging (MRI): cystic lesion on the left side of the L4–5 intervertebral disc, corresponding to the site of the previous endoscopic approach (red arrowhead). (A) Sagittal T2-weighted MRI, (B) Sagittal T1-weighted MRI, (C) Axial T2-weighted MRI, (D) Sagittal STIR (Short Tau Inversion Recovery) T2-weighted MRI.

During the operation, we encountered a structure resembling a chronic hematoma with a thickened capsule, containing a mixture of fluid and blood in a degenerative stage. This structure was located at the site of the previously removed disc herniation and was compressing the left L5 nerve root (Figure 3). After removing the PDP and excising the entire capsule, we used a radiofrequency coagulator for meticulous bleeding control and inserted a drain before closing the incision in the usual manner (Figure 4). The patient experienced complete improvement in left leg paresthesia immediately after surgery. MRI on the fifth postoperative day, before discharge, confirmed that the pseudocyst had been fully removed (Figure 5). Follow-up MRI 3-month postoperation showed no signs of PDP recurrence, and the patient’s symptoms had improved, with a VAS score of 1 (Figure 6).

Figure 3.

Dissection and removal of postoperative discal pseudocyst (PDP) via biportal endoscopic spinal surgery. (A) Exposure and identification of the boundary between the PDP and the dura mater (dotted black curve). (B) Retraction of the traversing nerve root (TNR) using a nerve root retractor. (C) Opening the capsule of the PDP. (D) Inspection inside the PDP and preparation for capsule removal. White star indicates nerve root retractor, black star indicates PDP, and red arrowhead indicates a structure resembling a chronic hematoma with a thickened capsule. RF, radiofrequency.

Figure 4.

After removal of the postoperative discal pseudocyst (PDP) and excision of the entire capsule. (A) Use of a radiofrequency (RF) coagulator for meticulous bleeding control. (B) RF to ablate the capsule of the PDP, specifically the portion adhering to the posterior of the intervertebral disc. (C) Confirmation that the entire PDP, including the capsule, has been completely removed before placing the drainage and insertion of a drain before closing the incision in the usual manner. Red arrowhead indicates capsule of the PDP after perforation with a Penfield dissector, black oval indicates the area after PDP removed and white star indicates nerve root retractor. TNR, traversing nerve root.

Figure 5.

Magnetic resonance imaging (MRI) on the fifth postoperative day, before discharge, confirming that the pseudocyst had been fully removed. (A) Sagittal T2-weighted MRI, (B) Sagittal T1-weighted MRI, (C) Axial T2-weighted MRI.

Figure 6.

Follow-up magnetic resonance imaging (MRI) 3-month postoperation showed no signs of postoperative discal pseudocyst recurrence. (A) Sagittal T2-weighted MRI, (B) Sagittal T1-weighted MRI, (C) Axial T2-weighted MRI (the red arrowhead indicates the complete removal of the PDP with no recurrence observed), (D) Sagittal STIR (Short Tau Inversion Recovery) T2-weighted MRI.

The patient provided written informed consent for the publication of this case report and accompanying images. In addition, this study was reviewed and approved by the Ethics Committee of Xuyen A Hospital (Approval number: 52/QD-BVXA2024).

DISCUSSION

1. Pathogenesis

PDP is an extremely rare complication following lumbar discectomy. The pathogenesis of this condition is not well understood and has not been thoroughly described. PDP was first reported by Young et al. [6] in 2009, who described 2 cases of PDP following microdiscectomy for LDH. The author originated the term “postoperative annular pseudocyst” to describe this condition, suggesting that the pseudocyst formation might result from the continued migration of miniscule disc fragments after surgery. These fragments may trigger a localized inflammatory response, leading to the development of a “pseudo-capsule” that encapsulates these disc fragments. Kono et al. [15] supported this hypothesis, reporting 2 cases of operatively confirmed discal cysts (DCs) and proposing that the pathogenesis of these cysts is similar to that of meniscal cysts in the knees and synovial cysts in the facet joints. They hypothesized that DC result from degeneration of the intervertebral disc, leading to herniation and the subsequent leakage of fluid from the herniated disc material. This extruded fluid triggers an inflammatory response, which leads to the formation of a reactive “pseudo-membrane” and the development of a DC. Similarly, Chiba's earlier understanding of the formation of spontaneous intraspinal cysts in the lumbar spine involves 3 factors: the resorption of a preexisting herniation, hematoma associated with disc prolapse, and mucoid degeneration, which is believed to be the cause of ganglion cysts in the peri-discal tissues [16].

Chung et al. [10] proposed that PDP formation is linked to axial loading on a mildly degenerated nucleus pulposus. This theory aligns with Aydin’s findings [17], which indicate that spontaneous DC occurs at a mean age of 33.5 years, significantly younger than typical cases of degenerative LDH, and is more common in physically active males. The authors suggest that, similar to spontaneous DC formation, in PDP, physical activity pumps fluid through an annular cleft in the degenerated nucleus, combine with a "pseudo-membrane" contributing to pseudocyst development.

In summary, there are 3 main hypotheses presented in the literature regarding the formation of PDP: a response to an epidural hematoma; pseudo-membrane formation following a local annulus fibrosus tear and disc degeneration; and an inflammatory response to the protrusion of tiny nucleus pulposus [7,10,15-17]. During revision surgery, we observed characteristics of PDP in our case that are consistent with these hypotheses. First, upon gross examination, the cyst appeared dark red, resembling the color of chronic hematoma, and was enclosed in a thick membranous structure. When we used a penfield to rupture the cyst and observed under endoscopic magnification, we noted that the cyst contained a mixture of materials, not merely fluid. This PDP was observed around the fourth week postoperatively, and MRI images showed that the cyst’s location was closely related to the disc space. Moreover, we believe that the PEID procedure, performed in a continuous water environment with pressure maintained around 30 mmHg, may have allowed water from the endoscopic system to infiltrate and remain within the already degenerated nucleus pulposus. Fibrin fibers formed from blood at the surgical site likely contributed to the formation of a membranous structure, preventing the escape and absorption of this fluid. These factors, combined with the mechanisms mentioned above, contribute to the formation of a thick-walled cystic structure (Figure 7). These hypotheses were reinforced when we performed a pathological examination of the removed cyst. The results revealed that the cyst wall had a heterogeneous structure, consisting of various components such as fibrous tissue, blood degradation products, and chronic inflammatory cells (Figure 8). This was similarly described in the report of Kang and Park [7].

Figure 7.

Illustration of the hypothesis for postoperative discal pseudocyst (PDP) formation after percutaneous endoscopic interlaminar discectomy. (A) Water enters the surgical field through the endoscope with medium pressure along the vertical axis, a small amount of this fluid may infiltrate the already degenerated disc nucleus. (B) A fibrin sheath formed by the inflammatory response and hematoma contributes to preventing the escape of this small amount of fluid. (C) Axial loading forces drive the retained fluid out of the disc nucleus, but it is blocked by the fibrin sheath, resulting in the formation of PDP.

Figure 8.

Pathological findings. The tissue exhibits a cystic structure with a fibrous wall accompanied by cholesterol crystals, old hemorrhage, and calcification. (A) Gross examination (original magnification ×40) shows three tissue samples, each measuring approximately 0.3–0.5 cm in diameter. (B) Microscopic examination (hematoxylin and eosin staining, original magnification ×100) demonstrates a cystic structure with a fibrous wall containing cholesterol crystals, old hemorrhage, and calcification. The cyst wall is infiltrated by chronic inflammatory cells and hemosiderin-laden giant cells.

2. Clinical Features

We summarized the literature of PDP in Table 1. Data were sourced from PubMed and Cochrane using keywords in the title and abstract, including "postoperative discal pseudocyst," "postoperative annular pseudocyst," "post discectomy pseudocyst," "postoperative pseudocyst," "pseudocyst," and "lumbar." The diagram showing the screening and selection of papers analyzed in the systematic literature review is presented as Figure 9. After screening, we identified 16 studies published in English up to 2023. The data show that regardless of the initial surgical technique—whether traditional open discectomy, microscopic, PEID, or percutaneous endoscopic transforaminal discectomy (PETD)—PDP formation is closely related to the location of the previous disc herniation. PDP may be asymptomatic and only detected through postoperative MRI, or it may cause symptoms ranging from mild to severe nerve root compression. Symptoms typically reappear within a few weeks postoperation. PDP occurs predominantly in males (84.7%) with an average age of 34.2 years.

Summary of the studies of postoperative discal pseudocyst found in a PubMed search

Figure 9.

Diagram showing the screening and selection of papers in the systematic literature review.

Chung's report on 12 PDP cases shows that after discectomy using microscopic or endoscopic, the mean time to relapsing radiculopathy was 23.3 days (range, 9–38 days) with an average VAS score of 6.8±1.3. PDP were detected on MRI at an average of 31.2 days (range, 14–60 days) after the initial surgery [10].

Manabe et al. [18] reported a case of a 21-year-old male requiring revision surgery for a PDP that developed 6 weeks after an endoscopic transforaminal L4–5 discectomy. Kang and Park [7] noted that PDP after endoscopic discectomy were reported at a 1% incidence in a study of 1,503 cases, with a mean postoperative interval of 53.7 days. The interlaminar approach showed a higher risk compared to the transforaminal approach, with 6 PDP occurring at L4–5 via transforaminal and 9 at L5–S1 via interlaminar out of 15 cases. The author did not establish whether differences between irrigation fluid and cystic fluid in these approaches contribute to this variation.

Among the 59 cases reported in the literature (Table 1), the highest incidence of PDP occurred after uniportal endoscopic lumbar discectomy (UELD), including both PETD and PEID, with 41 cases (69.5%) (Table 2). We did not find any report of PDP following biportal endoscopic lumbar discectomy (BELD). We believe that, although BELD is performed in a similar medium-pressure water environment as UELD, the distinct inflow and outflow pathways might contribute to a reduced residual water in the disc space during surgery. This could potentially explain the lower incidence of PDP observed. Figure 7 illustrates a hypothesis regarding the water flow during PEID surgery, which results in water retention in the degenerated nucleus pulposus and may be a contributing factor to the development of PDP.

Initial technique for lumbar discectomy

We categorized "initial technique using for lumbar discectomy" into 2 groups: endoscopic-related (group A) and nonendoscopic-related (group B). The rationale for this division is that spinal endoscopic surgeries are generally performed in a water environment with specific water pressure, which is different from traditional open and microscopic surgeries. The presence of a water environment in general and the maintained water pressure during the surgical process, in particular, may lead to the infiltration of water into the previously degenerated disc space, thereby increasing the risk of PDP formation. We observed a significant difference in the incidence of PDP between the 2 groups of initial techniques used for lumbar discectomy (p<0.001, chi-square test).

3. Management Strategies

Some cases have been reported to respond well to conservative treatment with NSAIDs, pain relief, and physical therapy [10,11,19-21]. Others may require simpler interventions, such as steroid injections and/or percutaneous cyst aspiration under fluoroscopic or CT guidance [6,10,22,23]. For cases with large cysts causing severe nerve root compression and not responding to conservative, surgical intervention to remove the pseudocyst may be necessary (Table 3). In most cases requiring revision surgery, authors prefer to use the same technique as was initially performed [9,12-14,24].

Management options for postoperative discal pseudocyst

Kang and Park [7] reported that 10 out of 15 cases improved with conservative treatment. The results showed no significant clinical differences between the groups requiring reoperation and those treated conservatively, with an average follow-up period of over 2 years. Jadhav et al.[11] also managed 4 cases—2 spontaneous DC and 2 PDP—conservatively using analgesia, neuropathic agents, and physiotherapy when needed, without strict bed rest. After 12 months of follow-up, all 4 patients showed clinical improvement, and the cysts spontaneously regressed on MRI. The author suggests that for patients with mild to moderate symptoms, conservative treatment should be the first option, as it can lead to significant improvement, even inducing spontaneous regression.

None of the cases requiring revision surgery in the literature reviewed reported subsequent recurrence of the PDP. In the study of Zhu et al. [12], reoperation was necessary in 13 out of 14 cases of PDP. Most of these PDP were larger than the previously excised herniated disc fragments. The author also noted a case that required PETD after an unsuccessful with percutaneous aspiration (PA). The author suggests that PA could be an alternative treatment with less trauma. However, C-arm or CT-guided aspiration and/or injection cannot remove the cyst wall, thereby risking recurrence of the pseudocyst. Additionally, complete aspiration may be difficult if the pseudocyst has a multi-cystic cavity.

PELD has been reported for the treatment of spontaneous DC and PDP via both the interlaminar and transforaminal approaches [7,8,12,13,18,24-27]. Wang et al. [13] presented 2 cases of PDP treated with PETD, where drainage was placed before closing the wound. In 1 case, the drain was removed on the seventh postoperative day, and in the other, on the fourth day. The author strongly recommends routine indwelling drainage during surgery to reduce nerve root irritation from local inflammatory factors and relieve radiculopathy. They also offered suggestions to prevent pseudocyst formation: (1) complete hemostasis during surgery and minimize coagulation and cauterization; (2) absolute bed rest on the first postoperative day; (3) wearing a lumbar brace for 2–3 months after surgery, along with moderate physical exercise. In our practice, we routinely place a drain in all cases of ED procedures (uniportal or biportal) and remove it on the second postoperative day. We believe this drainage helps reduce residual fluid at the surgical site, as water used during the endoscopic procedure may infiltrate and remain in the loose connective tissue around the spine. As mentioned earlier, when reoperating to remove the PDP, we prefer the BESS over PEID primarily to maintain a separate channel for water outflow, thereby reducing the risk of residual fluid in the surgical cavity.

CONCLUSION

PDP is an uncommon complication following lumbar discectomy, more frequently observed after the PELD procedure, particularly in younger male patients. Revision surgery is considered when the patient presents with symptoms of nerve root compression that are unresponsive to conservative management. The BESS technique offers an effective and safe option for reoperation to address PDP.

Notes

Conflict of Interest

The authors have nothing to disclose.

Funding/Support

This study received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.

Author Contribution

Conceptualization: TVHD, PAT; Data curation: TVHD, HVV, CVL, LTL; Formal Analysis: TVHD, LTL; Funding acquisition: TVHD, CVL; Methodology: TVHD, LTL; Project administration: TVHD, LTL; Visualization: TVHD; Writing – original draft: TVHD, HVV; Writing – review & editing: TVHD, PAT

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Article information Continued

Figure 1.

Preoperative magnetic resonance imaging (MRI): left-side L4–5 disc herniation (red arrowhead). (A) Sagittal T2-weighted MRI, (B) Sagittal T1-weighted MRI, (C) Axial T2-weighted MRI.

Figure 2.

Four-week postoperative magnetic resonance imaging (MRI): cystic lesion on the left side of the L4–5 intervertebral disc, corresponding to the site of the previous endoscopic approach (red arrowhead). (A) Sagittal T2-weighted MRI, (B) Sagittal T1-weighted MRI, (C) Axial T2-weighted MRI, (D) Sagittal STIR (Short Tau Inversion Recovery) T2-weighted MRI.

Figure 3.

Dissection and removal of postoperative discal pseudocyst (PDP) via biportal endoscopic spinal surgery. (A) Exposure and identification of the boundary between the PDP and the dura mater (dotted black curve). (B) Retraction of the traversing nerve root (TNR) using a nerve root retractor. (C) Opening the capsule of the PDP. (D) Inspection inside the PDP and preparation for capsule removal. White star indicates nerve root retractor, black star indicates PDP, and red arrowhead indicates a structure resembling a chronic hematoma with a thickened capsule. RF, radiofrequency.

Figure 4.

After removal of the postoperative discal pseudocyst (PDP) and excision of the entire capsule. (A) Use of a radiofrequency (RF) coagulator for meticulous bleeding control. (B) RF to ablate the capsule of the PDP, specifically the portion adhering to the posterior of the intervertebral disc. (C) Confirmation that the entire PDP, including the capsule, has been completely removed before placing the drainage and insertion of a drain before closing the incision in the usual manner. Red arrowhead indicates capsule of the PDP after perforation with a Penfield dissector, black oval indicates the area after PDP removed and white star indicates nerve root retractor. TNR, traversing nerve root.

Figure 5.

Magnetic resonance imaging (MRI) on the fifth postoperative day, before discharge, confirming that the pseudocyst had been fully removed. (A) Sagittal T2-weighted MRI, (B) Sagittal T1-weighted MRI, (C) Axial T2-weighted MRI.

Figure 6.

Follow-up magnetic resonance imaging (MRI) 3-month postoperation showed no signs of postoperative discal pseudocyst recurrence. (A) Sagittal T2-weighted MRI, (B) Sagittal T1-weighted MRI, (C) Axial T2-weighted MRI (the red arrowhead indicates the complete removal of the PDP with no recurrence observed), (D) Sagittal STIR (Short Tau Inversion Recovery) T2-weighted MRI.

Figure 7.

Illustration of the hypothesis for postoperative discal pseudocyst (PDP) formation after percutaneous endoscopic interlaminar discectomy. (A) Water enters the surgical field through the endoscope with medium pressure along the vertical axis, a small amount of this fluid may infiltrate the already degenerated disc nucleus. (B) A fibrin sheath formed by the inflammatory response and hematoma contributes to preventing the escape of this small amount of fluid. (C) Axial loading forces drive the retained fluid out of the disc nucleus, but it is blocked by the fibrin sheath, resulting in the formation of PDP.

Figure 8.

Pathological findings. The tissue exhibits a cystic structure with a fibrous wall accompanied by cholesterol crystals, old hemorrhage, and calcification. (A) Gross examination (original magnification ×40) shows three tissue samples, each measuring approximately 0.3–0.5 cm in diameter. (B) Microscopic examination (hematoxylin and eosin staining, original magnification ×100) demonstrates a cystic structure with a fibrous wall containing cholesterol crystals, old hemorrhage, and calcification. The cyst wall is infiltrated by chronic inflammatory cells and hemosiderin-laden giant cells.

Figure 9.

Diagram showing the screening and selection of papers in the systematic literature review.

Table 1.

Summary of the studies of postoperative discal pseudocyst found in a PubMed search

No. Study No. of patients Age (yr) Sex Initial technique Duration until radiculopathy recurred Management Journal
1 Young et al. [6] (2009) 2 60 M MD 1 Month 1 PA with disc biopsy Spine J
38 M 3 Weeks 1 PA with SJ
2 Kang and Park [7] (2011) 15 22.5±2.1 15 M 6 PETD 53.7±44.1 Days 10 Conservative J Korean Neurosurg Soc
9 PEID 4 PETD
1 PHL
3 Chung et al. [10] (2012) 12 29.3±11.9 11 M 9 MD 23.3 Days 6 Conservative Acta Neurochir
1 F 3 PELD 1 PA with SJ
5 Surgery (N/A)
4 Yu et al. [22] (2016) 1 27 M Open 2 Weeks PA with SJ Korean J Pain
5 Jha et al. [19] (2016) 2 16 M MED 1 Week 2 Conservative Asian J Endosc Surg
18 F 1 Week
6 Shiboi et al. [8] (2017) 2 27 M PETD 20 Days MED J Spine Surg
14 F 30 Days PETD
7 Manabe et al. [18] (2019) 1 21 M PETD 6 Weeks PETD Int J Spine Surg
8 Fu et al. [21] (2021) 1 23 M PELD 40 Days Conservative World J Clin Cases
9 Li et al. [23] (2021) 1 30 M PELD 37 Days Ozone ablation Medicine
10 Xu et al. [9] (2021) 1 27 M PEID 40 Days Cystectomy (N/A) Orthop Surg
11 Zhu et al. [12] (2022) 14 24.4 10 M PETD 43.5 Days 1 PA BMC Musculoskelet Disord
4 F 1 PA+PETD
2 PEID
10 PETD
12 Jadhav et al. [11] (2022) 2 27 1 M Open N/A Conservative J Surg Case Rep
1 F
13 Wang et al. [13] (2022) 2 24 2 M PETD 20 Days PETD with drainage catheter Medicine
34
14 Wang et al. [14] (2022) 1 25 M Open 45 Days Open (fusion) Medicine
15 Patgaonkar et al. [24] (2023) 1 35 F MD 2 Weeks PETD Surg Neurol Int
16 Bai and Sun [20] (2023) 1 25 M PEID 4 Months (asymptomatic) Conservative Quant Imaging Med Surg

MD, microdiscectomy; PA, percutaneous aspiration; SJ, steroid injection; PETD, percutaneous endoscopic transforaminal discectomy; PEID, percutaneous endoscopic interlaminar discectomy; PELD, percutaneous endoscopic lumbar discectomy; PHL, partial hemilaminectomy and discectomy; MED, microendoscopic discectomy; N/A, not available.

Table 2.

Initial technique for lumbar discectomy

Technique No. (%)
Endoscopic-related (group A)
 Uniportal (PETD and PEID) 41 (69.5)
 Microendoscopic discectomy 2 (3.4)
Nonendoscopic-related (group B)
 Microdiscectomy 12 (20.3)
 Traditional open discectomy 4 (6.8)

PETD, percutaneous endoscopic transforaminal discectomy; PEID, percutaneous endoscopic lumbar discectomy.

Table 3.

Management options for postoperative discal pseudocyst

Option No. (%)
Conservative 21 (35.6)
Interventional 6 (10.2)
Surgical 32 (54.2)

Intervention includes: PA, PA with SJ or ozone ablation.

PA, percutaneous aspiration; SJ, steroid injection.