COMPLEX REGIONAL PAIN SYNDROME FOLLOWING SPINAL DISEASES AND SURGERIES
PDF
Cite
Share
Request
Review Article
P: 257-264
October 2020

COMPLEX REGIONAL PAIN SYNDROME FOLLOWING SPINAL DISEASES AND SURGERIES

J Turk Spinal Surg 2020;31(4):257-264
1. Near East University School of Medicine, Department of Anaesthesiology and Reanimation, Pain Clinic, Nicosia, Northern Cyprus, Turkey
No information available.
No information available
Received Date: 05.10.2020
Accepted Date: 29.10.2020
Publish Date: 18.11.2020
PDF
Cite
Share
Request

ABSTRACT

Complex regional pain syndrome (CRPS) impairs the patient’s active life and his/her psychological state due to reductions in functional movements, severe pain, and muscle atrophy. Fractures and surgical operations are important risk factors for CRPS, and several studies reported incidences of CRPS following surgical procedures to the upper or lower limb. CRPS can also be seen after spinal diseases and surgeries, yet the literature includes only limited number of studies in this area and there are not enough works considering incidence of CRPS following spinal problems. While early diagnosis and appropriate treatment of CRPS in acute period are very important for prevention of chronic symptoms (including allodynia, swelling, muscular atrophy, osteoporosis and contracture), clinicians need to be aware that the spinal problems may cause CRPS. The aim of this review is to emphasize the possibility of CRPS development after spinal diseases or surgeries and strongly argue that the diagnosis of CRPS following spinal problems must be considered by clinicians.

Keywords:
Complex regional pain syndrome, spinal disease, spinal surgery, spinal cord injury, spinal tumor

INTRODUCTION

Complex regional pain syndrome (CRPS) impairs the patient’s active life and his/her psychological state due to reductions in functional movements, severe pain and muscle atrophy. CRPS is characterised by a severe, generally not well-tolerated, pain that usually involves the extremities. The most significant complaints are severe pain with edema and other vasomotor and motor symptoms, such as temperature and/or skin colour asymmetry, dystonia and tremor. Although current medical treatments often target acute symptoms, CRPS can also become chronic, lasting for months or years, accompanied with other symptoms due to irregularities in the sympathetic nervous system. Even though CPRS can be characterised as a chronic neurological disease, it is generally caused by a triggering trauma, such as fractures, surgeries or even minor injuries.

Acute and Chronic CRPS

CRPS may be categorised into two: CRPS type 1 may occur without nerve lesions and CRPS type 2 is associated with nerve lesions caused by a triggering trauma(1,2). Even in the absence of nerve damage, a triggering trauma and subsequent flared posttraumatic inflammation may be observed. The progression of this syndrome is variable, but the clinical presentation is often similar in both groups: in the acute period, common features include the five main signs of inflammation, namely, pain, edema, erythema, changes in skin temperature/colour and dysfunction(2). In fact, the transient features of CRPS may be observed more commonly than most clinicians realise and CRPS may even occur after minor limb injuries. As CRPS becomes chronic, symptoms can evolve, and allodynia, sweating, dystonia and muscle atrophy may occur during the disease course. During this period, symptoms may appear exaggerated and disproportionate in degree and duration with respect to the triggering event, and chronic symptoms of CPRS can no longer be explained by the initial trauma.

Vasomotor dysfunction is common in patients with CRPS. While the affected limb is generally warmer than the healthy limb at earlier stages, it becomes colder in the later phases of the syndrome(2). While red and hot lesions are observed in the acute phase, if the patient is not treated appropriately, the drop in the skin temperature of the affected area can result in cold lesions in the chronic phase.

Importance of Early Treatment of CRPS

In patients with CRPS, symptoms tend to begin during the first month following trauma and/or immobilisation of the extremity(3); physical problems may begin approximately 2 years after disease onset(4,5). Since CRPS has no known evidence-based effective treatment, approximately 15% of the patients experience unbearable pain. If CRPS is not properly treated in the acute period (3–6 months from onset), tendons may shorten and fibrosis may develop(6);  thus, contractures may occur very quickly.

In chronic CRPS, symptoms can lead to complete disruption of normal daily activities due to severe pain and atrophy in the affected limb. This may lead to excessive use and abuse of drugs for CRPS treatment(3,7), and drug side effects may be observed. In particular, long-term and high-dose usage of opioids may cause severe problems due to tolerance, dependence, immune suppression and dysfunction in the endocrine system. Long-term usage of opioids may also cause hyperalgesia(8). Respiratory suppression due to opioid overdose may result in death.

Delayed and insufficient treatment may increase the risks of complete deterioration in daily activities, major depression and suicide(7). If treatment options are ineffective, amputation may be required; physical and psychological problems in CRPS may become so severe that clinical teams encountered patients who requested limb amputation(1). However, even after such a drastic intervention, phantom pain (77% of the cases)(9) and CRPS recurrence in the remaining extremity (24% of the cases)(10) remain as potential risks.

As presented above, early treatment of CRPS is very important in preventing long-term symptoms (allodynia, muscular atrophy, etc.); thus, clinicians must start appropriate treatment protocols without any delay when early diagnosis of CRPS is possible(11). Unfortunately, CRPS is not easy to diagnose.

Early Diagnosis of CRPS

Early diagnosis of CRPS may prevent long-term complications and sequelae, including muscle atrophy, osteoporosis, joint stiffness, tendon shortening and contracture, which weaken the patient’s active life by reducing his/her functional movements. A major problem with the diagnosis of CPRS is that symptoms can mimic other diseases. Diagnosis relies on clinical findings; unfortunately, a gold standard and objective diagnostic test for CRPS is not yet established. CRPS is diagnosed clinically using the diagnostic criteria of the International Association for the Study of Pain (Budapest Diagnostic Criteria for CRPS)(7,12).

Table 1 lists some of the diagnostic signals that should be considered(3). During differential diagnosis, especially for complex cases, imaging tests (including magnetic resonance imaging and computed tomography) may be performed to exclude other possible diseases. Plain film may also be used, except in extreme cases (Sudeck’s atrophy).

Table 1

Electromyography and nerve conduction studies may help assess the presence of nerve injury and muscle fibre loss. Three-phase bone scintigraphy may detect trophic changes of the bone. Local anaesthetic sympathetic blocks are commonly used for diagnostic purposes. If a patient has a good response to a diagnostic sympathetic block with local anaesthetic, sympathetic denervation through radiofrequency ablation can be offered for therapeutic purposes.

Since CRPS symptoms are similar to that of other diseases, patients often undergo evaluation by multiple specialists before the final diagnosis is confirmed, and this may lead to significant delays in treatment. These delays may also increase the risk of the disease becoming chronic and may lead to serious economic losses for the patient.

Risk Factors for CRPS and Incidence of CRPS after Fractures/Surgeries

Common risk factors for CPRS are listed in Table 2(13-17). According to de Mos et al.(14), women are three times more affected by CPRS than men. Individuals aged 61–70 years are most commonly affected, and the risk is highest in postmenopausal women. According to the same study, the upper limb is affected more frequently than the lower limb, and the most common trigger events are fractures, accounting for 44% of the cases. As shown in Table 3(18-23) and Table 4(23-34), several studies reported a high incidence of CRPS, especially after distal radius fracture (32.2%), Colles’ fracture (36.7%), tibial fracture (30%) and shoulder (11.1%) and tibial (31%) surgeries(1). Unfortunately, CPRS-related complications following orthopaedic surgeries may negatively affect the postoperative healing process, and the syndrome may lead to serious long-term problems, including unbearable pain and immobilisation.

Table 2
Table 3
Table 4

While there is a strong evidence of CRPS incidence following fractures and surgical operations, there is little prior work on the incidence of CRPS following spinal surgeries. Most studies indicating potential presence of CRPS following spinal diseases and surgeries are based on case studies.

METHODS

This study aimed to present a review of the literature on CRPS occurrence following spinal problems and surgeries to improve physicians’ awareness of this. For this review, we combed the published literature for studies of patients who developed CPRS after three main spinal problems, including degenerated/herniated disc surgeries, spinal cord injury (SCI) and spinal cord tumor. Published studies were grouped under these three categories and further investigated according to the type of CRPS (1 or 2), disease origin and grade, type of surgeries prior to CRPS onset, disease course, therapies following diagnosis of CRPS and age (ranged from 22 to 69 years) and sex of the patients. We also focused on the reported progress of the disease after therapy.

DISCUSSION

CRPS following Degenerated and Herniated Disc Surgeries

Table 5 lists several studies that report CRPS cases following spinal diseases/procedures. These studies highlight the possibility of CRPS associated with spinal procedures and the importance of early treatment for effective results.

Table 5

Plancarte and Calvillo(35) reported a patient with CRPS type 2, following automated laser discectomy, who presented sympathetically maintained pain and serious disability. The author suggested that CRPS can be associated with spinal procedures, including automated laser percutaneous discectomy. In another case study, Fish presented a patient with CRPS type 2 in a distal extremity associated with an anterior sacroiliac fusion with local bone graft(36). Fish argued that CRPS can be associated with spinal procedures and sacroiliac arthrodesis. Both Plancarte and Fish concluded that early intervention is important in long-term resolution of CRPS symptoms.

Knoeller at al.(37) reported a case of CRPS 1 of the left leg following lumbar spine surgery (implantation of an artificial disc type in the L4-5 segment) using a midline left-sided retroperitoneal approach via a ventral access (this surgery requires mobilisation of the sympathetic trunk). The report emphasised that diagnosis of CRPS following lumbar spine surgery via a ventral access must be considered a differential diagnosis, and Knoeller at al.(37) highlighted the importance of early diagnosis, as early initiation of therapy in CRPS type 1 may improve the progress of a disabling severe disease.

Chae et al.(38) reported about CRPS type 2 following a postoperative lumbar spine surgery and pointed out the importance of distinguishing CRPS symptoms from postoperative symptoms. Despite the difficulty in differentiating postoperative syndrome in the lumbar spine from CRPS, they recommended that physicians should consider CRPS as the primary cause of postoperative syndrome in the lumbar spine after orthopaedic surgery, as this may prevent significant losses in time before the start of an effective treatment.

Similarly, Jung et al.(39) noted that CRPS-like symptoms can appear after lumbar spinal surgery due to adhesion and inflammation in the epidural space. They reported the case of a 31-year-old patient diagnosed with CRPS type 2 following L5-S1 discectomy. Unfortunately, the patient did not respond to conventional therapies or to spinal cord stimulation for the treatment of CRPS. Consequently, for diagnostic and therapeutic purposes, sacral epiduroscopic laser decompression (SELD) was performed twice 1 month apart. During these procedures, severe adhesion and inflammation at the L4-S1 epidural space were detected. The catheter was placed to perform mechanical adhesiolysis and laser decompression at the herniated intervertebral disc. Three days after the second intervention, the visual analogue scale (VAS) score had improved, and 8 months later, the patient reported complete absence of pain. The authors suggested that if CRPS-like symptoms originating from the lumbar spine cannot be treated by conventional therapy, SELD may be considered an appropriate diagnostic and therapeutic option.

More recently, Wolter et al.(40)carried out a study to determine the frequency of CRPS following spinal surgery and to investigate the disease course and prognostic factors. 35 patients (18 women and 17 men) who were treated for CRPS (1 or 2) were included in the study. The authors considered the CRPS type, disease origin and grade and type of surgeries prior to CRPS onset. Table 6 reports data regarding six patients (one patient had cervical and five patients had lumbar spine surgery) who had undergone spinal operations just before the onset of CRPS symptoms (median, 5 days; range: 1–14) and had no other trauma preceding the development of CRPS symptoms. As shown, CRPS symptoms following spinal surgery can start very quickly. Consequently, the authors concluded that even if CRPS may occur relatively rarely following spinal surgeries, physicians must be aware of the possibility of CRPS, as early diagnosis and treatment are important to prevent complications.

Table 6

Most studies about CRPS following spinal problems focus on lumbar disc protrusion and lumbar spinal surgery. In Wolter et al.(40), only one patient had cervical surgery before CRPS. Weisz et al.(41) reported the case of a 39-year-old patient who had shown CRPS symptoms following cervical spine surgery (posterior foraminotomy at C5–6 and C6–7). Following the surgery, the patient experienced pain, paraesthesia, swelling of the left hand and forearm and increasing inability to use the left hand; as a result, the patient was diagnosed with CRPS. The treatment included opioids, tricyclics and hypnotics on a daily basis, which improved physical features and associated psychological and social problems. 34 months after surgery, symptoms remained less intense; however, several features of CRPS (swelling, paleness and cold and wet skin) were still evident.

Kim et al.(42) reported a case of CRPS that was caused by L4–5 herniated intervertebral disc without a history of trauma or surgery. Percutaneous nucleoplasty was considered as a treatment option for CRPS, after which the symptoms were relieved and the VAS score had improved. While CRPS from a mild herniated intervertebral disc without surgical intervention is even rarer than CRPS after surgery for disc diseases, this possibility should be kept in mind during differential diagnosis.

CRPS in Spinal Cord Injury

Pain is a frequent complication of SCI, and identifying the possible causes of the pain is very important for effective treatment. While neurological problems like stroke and peripheral nerve injuries are known etiological causes of CRPS, several studies reported CRPS also in patients with SCI(43-47). Table 7 summarises the key findings of some of these case studies.

Table 7

Gellman et al.(44) studied 60 patients with cervical SCI and identified an overall incidence rate of 10% of CRPS. Lefkoe and Cardenas(45) presented the case of a 25-year-old tetraplegic male patient with complete traumatic injury of the cervical cord (C6) who presented CRPS. In addition, Lefkoe and Cardenas(45) pointed out that in patients with SCI, diagnosis of CRPS might be challenging due to the presence of severe pain and other common CRPS complications, such as heterotopic ossification or deep venous thrombosis in SCI patients without CRPS.

Gallien et al.(46) reported eight CRPS cases in a study of patients with SCI. The study included one female and seven male patients, with a median age of 35. The causes of SCI included gunshot wounds (n=5), car accidents (n=2) and fall (n=1). Five patients had complete SCI, and three patients had incomplete SCI. Four patients were tetraplegic, while four patients were paraplegic. The authors discussed the diagnosis, risk factors and treatment and concluded that, even if this syndrome may be more common in other forms of neurological diseases, such as stroke, CRPS might also be observed as the main source of pain in patients with SCI.

Sutbeyaz et al.(47) reported the case of a 49-year-old man with C7 incomplete tetraplegia who presented CRPS type 1 in both upper and lower extremities. The authors emphasised that CRPS type I might be more common in SCI than usually suspected and that tetraplegic patients should be carefully evaluated for the presence of CRPS type I.

CRPS in Spinal Cord Tumor

We have found only one published case of a patient with cervical spinal cord tumor (schwannoma) and CRPS type 2(48). This 63-year-old patient underwent urgent neurosurgery, and the spinal lesion was excised. At 6 weeks after the procedure, the symptoms had completely disappeared. After 1 year, the patient was still completely asymptomatic.

CONCLUSION

Early diagnosis and proper treatment of acute CRPS are very important in preventing the development of chronic symptoms (including allodynia, swelling, muscular atrophy, osteoporosis and contracture). Clinicians must be aware of the potential scenarios in which patients may develop CRPS. Fractures and surgical operations are critical risk factors for CRPS. In this review, we emphasised the possibility of CRPS development after spinal diseases and/or surgeries. While the literature on CRPS following spinal problems consists primarily of small case studies and there are limited data on the incidence of CRPS following spinal problems, there is growing evidence that CRPS may also occur after spinal diseases or surgeries and that the diagnosis of CRPS following spinal problems must be considered by clinicians.

References

1
Goh EL, Chidambaram S, Ma D. Complex regional pain syndrome: a recent update. Burns Trauma. 2017;5:2.
2
Marinus J, Moseley GL, Birklein F, Baron R, Maihöfner c, Kingery WS, et al. Clinical features and pathophysiology of complex regional pain syndrome. Lancet Neurol. 2011;10:637-48.
3
Goebel A, Barker CH, Turner-Stokes L et al. “Complex Regional Pain Syndrome in Adults: UK guidelines for diagnosis, referral and management in primary and secondary care. London: Royal College of Physicians, 2018; https://www.rcplondon.ac.uk/guidelines-policy/complex-regional-pain-syndrome-adults
4
de Mos M, Huygen FJ, van der Hoeven-Borgman M, Dieleman JP, Ch Stricker BH, Sturkenboom MC. Outcome of the complex regional pain syndrome. The Clin J Pain. 2009;25:590-7.
5
Schasfoort FC, Bussmann JB, Stam HJ. Impairments and activity limitations in subjects with chronic upper-limb complex regional pain syndrome type I. Arch Phys Med Rehabil. 2004;85:557-66.
6
Winston P. Early treatment of acute complex regional pain syndrome after fracture or injury with prednisone: why is there a failure to treat? A case series. Pain Res Manag. 2016:1-5.
7
International Association for the Study of Pain, Subcommittee on taxonomy. Description of chronic pain syndromes and definitions of pain terms. Pain. 1986;(Suppl 3):S28-30.
8
Roeckel LA, Le Coz GM, Gavériaux-Ruff C, Simonin F. Opioid-induced hyperalgesia: Cellular and molecular mechanisms. Neuroscience. 2016;338:160-82.
9
Bodde MI, Dijkstra PU, Schrier E, van den Dungen JJ, den Dunnen WF, Geertzen JH. Informed Decision-Making Regarding Amputation for Complex Regional Pain Syndrome Type I. J Bone Joint Surg Am. 2014;96:930-4.
10
Krans-Schreuder HK, Bodde MI, Schrier E, Dijkstra PU, van den Dungen JA, den Dunnen WF, et al. Amputation for long-standing, therapy-resistant type-I complex regional pain syndrome. J Bone Joint Surg Am. 2012;94:2263-8.
11
Bussa M, Guttilla D, Lucia M, Mascaro A, Rinaldi S. Complex regional pain syndrome type I: a comprehensive review. Acta Anaesthesiol Scand. 2015;59:685-97.
12
Birklein F, Dimova V. Complex regional pain syndrome-up-to-date. Pain Rep. 2017;2:e624.
13
An HS, Hawthorne KB, Jackson WT. Reflex sympathetic dystrophy and cigarette smoking. J Hand Surg. 1988;13:458-60.
14
de Mos M, de Bruijn AG, Huygen FJ, Dieleman JP, Stricker BH, Sturkenboom MC. The incidence of complex regional pain syndrome: a population-based study. Pain. 2007;129:12-20.
15
de Mos M, Huygen FJ, Dieleman JP, Koopman JS, Stricker BH, Sturkenboom MC. Medical history and the onset of complex regional pain syndrome (CRPS). Pain. 2008;139:458-66.
16
de Mos M, Huygen FJ, Stricker BH, Dieleman JP, Sturkenboom MC. The association between ACE inhibitors and the complex regional pain syndrome: Suggestions for a neuro-inflammatory pathogenesis of CRPS. Pain. 2009;142:218-24.
17
Sandroni P, Benrud-Larson LM, McClelland RL, Low PA. Complex regional pain syndrome type I: incidence and prevalence in Olmsted county, a population-based study. Pain. 2003;103:199-207.
18
Jellad A, Salah S, Frih ZBS. Complex regional pain syndrome type I: incidence and risk factors in patients with fracture of the distal radius. Arch Phys Med Rehabil. 2014;95:487-92.
19
Dijkstra PU, Groothoff JW, Duis HJ, Geertzen JHB. Incidence of complexregional pain syndrome type I after fractures of the distal radius. Eur J Pain. 2003;7:457-62.
20
Bickerstaff DR, Kanis JA. Algodystrophy: an under-recognized complication of minor trauma. Br J Rheumatol. 1994;33:240-8.
21
Atkins RM, Duckworth T, Kanis JA. Features of algodystrophy after Colles’ fracture. J Bone Joint Surg. 1990;72:105-10.
22
Beerthuizen A, Stronks DL, van’t Spijker A, Yaksh A, Hanraets BM, Klein J, et al. Demographic and medical parameters in the development of complex regional pain syndrome type 1 (CRPS1): prospective study on 596 patients with a fracture. Pain. 2012;153:1187-92.
23
Sarangi PP, Ward AJ, Smith EJ, Staddon GE, Atkins RM. Algodystrophy and osteoporosis after tibial fractures. J Bone Joint Surg. 1993;75:450-2.
24
Chalmers PN, Slikker Iii W, Mall NA, Gupta AK, Rahman Z, Enriquez D, et al. Reverse total shoulder arthroplasty for acute proximal humeral fracture: comparison to open reduction–internal fixation and hemiarthroplasty. J Shoulder Elb Surg. 2014;23:197-204.
25
Arndt J, Clavert P, Mielcarek P, Bouchaib J, Meyer N, Kempf JF. Immediate passive motion versus immobilization after endoscopic supraspinatus tendon repair: a prospective randomized study. Affiliate Societies. 2012;98(6 Suppl):S131–8.
26
Gonzalez J-F, Alami GB, Baque F, Walch G, Boileau P. Complications of unconstrained shoulder prostheses. J Shoulder Elb Surg. 2011;20:666–82.
27
Bishop JY, Sprague M, Gelber J, Krol M, Rosenblatt MA, Gladstone J, Flatow EL. Interscalene regional anesthesia for shoulder surgery. J Bone Joint Surg Am. 2005;87:974–9.
28
Borgeat A, Ilfeld BM, Ekatodramis G, Singelyn FJ, Seguy S, Gouverneur JM, et al. Acute and non-acute complications associated with interscalene block. Anesthesiology. 2001;95:875–80.
29
Shinya K, Lanzetta M, Conolly WB. Risk and complications in endoscopic carpal tunnel release. J Hand Surg. 1995;20:222–7
30
Lichtman DM, Florio RL, Mack GR. Carpal tunnel release under local anesthesia: evaluation of the outpatient procedure. J Hand Surg.1979;4:544–6.
31
MacDonald RI, Lichtman DM, Hanlon JJ, Wilson JN. Complications of surgical release for carpal tunnel syndrome. J Hand Surg. 1978;3:70–6.
32
Lilly SI, Stern PJ. Simultaneous carpal tunnel release and Dupuytren’sf asciectomy. J Hand Surg. 2010;35:754–9.
33
Bulstrode NW, Jemec B, Smith PJ. The complications of Dupuytren’s contracture surgery. J Hand Surg. 2005;30:1021–5.
34
Rewhorn MJ, Leung AH, Gillespie A, Moir JS, Miller R. Incidence of complex regional pain syndrome after foot and ankle surgery. J Foot Ankle Surg. 2014;53:256–8.
35
Plancarte R, Calvillo O. Complex regional pain syndrome type 2 (causalgia) after automated laser discectomy: A case report. Spine (Phila Pa 1976). 1997;22:459-62.
36
Fish DE. Post-lumbar surgery complex regional pain syndrome. Pain Physician. 2005;8:319-22.
37
Knoeller SM, Ehmer M, Kleinmann B, Wolter T. CRPS I following artificial disc surgery: case report and review of the literature. Eur Spine J. 2011;20 Suppl 2(Suppl 2): S278-83.
38
Chae SU, Kim TK, Shim DM, Kim YJ, Choi DH. Is complex regional pain syndrome a cause of post-operative syndrome in the lumbar spine? - a case report -. Asian Spine J. 2009;3:101-5.
39
Jung JW, Kim YH, Kim H, Kang E, Jo H, Ko MJ. Sacral epiduroscopic laser decompression for complex regional pain syndrome after lumbar spinal surgery: A case report. Medicine (Baltimore). 2018;97:e0694.
40
Wolter T, Knöller SM, Rommel O. Complex regional pain syndrome following spine surgery: clinical and prognostic implications. Eur Neurol. 2012;68:52-8.
41
Weisz GM, Houang M, Bogduk N. Complex regional pain syndrome associated with cervical disc protrusion and foraminotomy. Pain Med. 2010;11:1348-51.
42
Kim SH, Choi SS, Lee MK, Kin JE. Complex regional pain syndrome caused by lumbar herniated intervertebral disc disease. Pain Physician. 2016;19:E901-4.
43
Akkoc Y, Uyar M, Oncu J, Ozcan Z, Durmaz B. Complex regional pain syndrome in a patient with spinal cord injury: management with pulsed radiofrequency lumbar sympatholysis. Spinal Cord. 2008;46:82-4.
44
Gellman H, Eckert RR, Botte MJ, Sakimura I, Waters RL. Reflex sympathetic dystrophy in cervical spinal cord injury patients. Clin Orthop Relat Res. 1988:126-31.
45
Lefkoe TP, Cardenas DD. Reflex sympathetic dystrophy of the lower extremity in tetraplegia: case report. Spinal Cord. 1996;34:239-42.
46
Gallien P, Nicolas B, Robineau S, Lebot MP, Brissot R. The reflex sympathetic dystrophy syndrome in patients who have had a spinal cord injury. Paraplegia. 1995;33:715-20.
47
Sutbeyaz ST, Koseoglu BF, Yeşiltepe E. Simultaneous upper and lower extremity complex regional pain syndrome type I in tetraplegia. Spinal Cord. 2005;43:568-72.
48
Regan MJ, Rathi J. Cervical spinal cord tumor causing complex regional pain syndrome. Mayo Clin Proc. 2011;86:713.