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Bilateral complex regional pain syndrome associated with lumbar disc herniation / lomber disk hernisi ile iliskili iki tarafli kompleks bolgesel agri sendromu.

Causalgia or complex regional pain syndrome (CRPS)-type II is a syndrome formed by a combination of pain, trophic changes and vasomotor disturbances. This syndrome is characterized by pain on active or passive movement, abnormal regulation of blood flow and sweating, and edema of skin and subcutaneous tissues. (1) It is self-limiting in some individuals which results in long-lasting impairment for some and disability in others. (2)

Although cases describing CRPS secondary to lumbar disc herniation (LDH) are abundant in the literature, (3 -9) CRPS in these reports developed in association with LDH or after disc surgery in one extremity. To our knowledge, based on our review of the literature, we have not found any case of bilateral CRPS in the lower extremities associated with LDH and hereby present the first such case which was successfully treated conservatively.

CASE REPORT

A 49-year-old man complained of pain and swelling of the feet and ankles, particularly on the left side. Two months previously, he had experienced an episode of low back pain radiating down the left leg which developed after an episode of bending and lifting. At that time, he was diagnosed with LDH which was confirmed by magnetic resonance (MR) imaging. The lumbar spine MR images showed L5-S1 disc protrusion in the posterocentral region and in bilateral paramedian regions which was more apparent on the right side (Figure 1). His pain decreased after several days of bed rest and analgesic treatment. One month later low back pain, aching and stiffness developed in the joints of both ankles and feet and was accompanied by dorsal hyperalgesia and allodynia of the left foot. The aching was exacerbated by local pressure or attempted foot movement. Over the next month the symptoms steadily worsened to the point of an inability to bear any weight on the right foot. Mild swelling of the feet, edema, and hyperhydrosis of the left foot were also noted. Ankle motion was restricted near the end of range. There was a complaint of low back discomfort. Straight leg raising on the left side was only 45 degrees. There was a suggestion of mild plantar flexor weakness (4/5, 0 to 5 scale) on the left, but extreme pain on palpation of the left lower extremity prevented reliable motor strength and sensorial evaluation. The remainder of the neuromuscular examination was unremarkable. Rectal tone was intact, and pulses were normal. The patient had no history of trauma. Past medical history, family history and a review of systems were unremarkable revealing no indication of endocrine, rheumatologic or other systemic diseases.

[FIGURE 1 OMITTED]

Routine laboratory investigations disclosed no abnormalities. Electromyography disclosed involvement of the left S1 root (gastrocnemius muscle had 2+ waves with mild decreased motor unit numbers) and corresponding paraspinal muscles suggestive of preganglionic damage; sensory and motor conduction was normal. Foot radiographs showed a pattern of osteopenia consistent with left CRPS (Figure 2). Technetium-99m methylene diphosphonate (Tc-99m MDP) three-phase bone scintigraphy (TPBS) confirmed the clinical diagnosis of bilateral CRPS by detecting the mild or intense increased activity uptake in a dynamic, early blood pool, especially in delayed static images (Figure 3).

[FIGURE 2 OMITTED]

[FIGURE 3 OMITTED]

Comprehensive conservative therapy was commenced consisting of drug treatment (non steroidal anti-inflammatory drug [NSAID], gabapentin and calcitonin nasal spray), an outpatient rehabilitation program involving active and passive range of motion to both ankles with gentle stretching, desensitization activities (including contrast baths), gait training, and a physical therapy program involving hot packs, ultrasound and TENS to the lumbar region. Three weeks later, the back pain was totally relieved and lower extremity symptoms were mainly relieved in six weeks. There was no residual foot stiffness, swelling, edema or any atrophic changes. Electromyography six months after therapy showed a decrease in denervation. No recurrence occurred after a follow-up of 12 months.

DISCUSSION

Causalgia or complex regional pain syndrome is a painful syndrome affecting one or more extremities of the body and is marked by a wide variety of symptoms. (10) Jinkins et al. (11) proposed an anatomic basis for a link between CRPS and disc herniation. The complex neural interconnections between somatic and autonomic nervous systems account for the nonspecific pain and referred autonomic dysfunction that may be represented in the form of abnormal vasomotor, pilomotor and sudomotor activity occasionally associated with LDH. (9), (11)

The pathogenesis of CRPS evolves from disturbances in both the peripheral and central nervous systems. Interest has recently increased in the role of inflammatory responses in the initial phase of the disorder. Inflammatory signs such as swelling, redness, warmth and pain are common features in the early stage of CRPS. In addition to classic inflammation, neurogenic inflammation has been demonstrated in CRPS. Neurogenic inflammation resembles classic inflammation but is initiated by neuropeptides instead of lymphocytes and cytokines. (10), (12)

Causalgia or complex regional pain syndrome is usually described after a specific initiating event (in most cases trauma or an operation), but it is sporadically observed after a stroke, myocardial infarction and infection. (13) The CRPS-type II which develops after a nerve lesion is by definition a neuropathic pain syndrome. (1) Although the actual incidence of CRPS-type II is unknown, it is estimated to occur in at least 1% to 5% of patients who have incurred a peripheral nerve injury. (2)

This entity is common in the limbs and is characterized by pain (spontaneous pain, hyperalgesia, allodynia), active and passive movement disorders, abnormal regulation of blood flow and sweating, edema of skin and subcutaneous tissues, and trophic changes of skin, organs of skin and subcutaneous tissues. (1) Upper extremity CRPS-type II is most frequently caused by injury to the brachial plexus or median nerve. Lower extremity CRPS-type II is typically caused by injury to the sciatic or tibial nerve. (2) In the literature, CRPS secondary to LDH is common and occurred in only one extremity. (3-9) Some of the reported cases are secondary to LDH, (3), (4), (7-9) and others are secondary to operated LDH. (3), (4), (6) Except for a single case of CRPS treated with sympathetic block, (8) all other reported CRPS cases regressed symptomatically after surgical treatment of herniation. (3), (4), (7), (9) We report the only case of bilateral CRPS in the lower extremities due to LDH that was treated conservatively. One explanation for CRPS being bilateral in our case could be the presence of bilateral lumbar disc protrusion with right-sided predominance which clinically presented itself with pain radiating to the left leg. The other explanation could be immobilization of both legs during the bed rest period.

The characteristicappearanceoftheroentgenogram in CRPS is that of extensive mottled demineralization. The TPBS is valuable, particularly in mild or early cases of CRPS where roentgenograms of the extremities may be negative. (3) In our case, direct radiography showed the characteristic appearance only on the left foot, but the right foot appeared normal. In the early period when the right foot appeared normal on radiographs, the bilateral occurrence of CRPS was detected by the TPBS showing the mild or intense increased activity uptake in a dynamic, early blood pool, especially in delayed static images. (3), (14) While symptoms of CRPS associated with LDH in the literature either begin or subside with a disc operation, (3-7), (9) conservative measures relieved both the LDH and the CRPS in our case. The symptoms in our case resolved with medical therapy consisting of NSAIDs, calcitonin and gabapentin in addition to a rehabilitation program including exercise and physical therapy.

The treatment of CRPS-type II is most successful when performed early in the course of the syndrome, preferably within three months after onset. Early diagnosis is therefore crucial. (2) A delay in diagnosis and/or treatment for this syndrome can result in severe physical and psychological problems. (15) We propose that early diagnosis (aided by TPBS) of CRPS in our case (one month after the onset of symptoms) added to the success of conservative treatment.

Causalgia or complex regional pain syndrome is a challenging pain syndrome which can be severe and functionally debilitating. It should be considered as a cause of bilateral, persistently painful and swollen extremities in a patient with LDH. Early, accurate diagnosis permits initiation of appropriate therapeutic interventions and enhances the potential for successful treatment.

Declaration of conflicting interests

The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.

Funding

The authors received no financial support for the research and/or authorship of this article.

REFERENCES

(1.) Janig W, Baron R. Complex regional pain syndrome: mystery explained? Lancet Neurol 2003;2:687-97.

(2.) Bryant PR, Kim CT, Millan R. The rehabilitation of causalgia (complex regional pain syndrome-type II). Phys Med Rehabil Clin N Am 2002;13:137-57.

(3.) Carlson DH, Simon H, Wegner W. Bone scanning and diagnosis of reflex sympathetic dystrophy secondary to herniated lumbar disks. Neurology 1977;27:791-3.

(4.) Ballard EM, Ellenberg M, Chodoroff G. Reflex sympathetic dystrophy syndrome secondary to L5 radiculopathy. Arch Phys Med Rehabil 1991;72:595-7.

(5.) Chodoroff B, Ball RD. Lumbosacral radiculopathy, reflex sympathetic dystrophy and tarsal tunnel syndrome: an unusual presentation. Arch Phys Med Rehabil 1985;66:185-7.

(6.) Sachs BL, Zindrick MR, Beasley RD. Reflex sympathetic dystrophy after operative procedures on the lumbar spine. J Bone Joint Surg [Am] 1993;75:721-5.

(7.) Condon F, Kenny PJ, Griffin JG, O'Rourke K. Reflex sympathetic dystrophy associated with extraforaminal disc herniation at the L5-S1 level. J Spinal Disord 1998; 11:448-51.

(8.) Adachi M, Tamaoka A, Harada K, Mizusawa H, Shoji S. Reflex sympathetic dystrophy secondary to lumbar disk herniation. Rinsho Shinkeigaku 1994;34:61-4. [Abstract]

(9.) Bernini PM, Simeone FA. Reflex sympathetic dystrophy associated with low lumbar disc herniation. Spine (Phila Pa 1976) 1981;6:180-4.

(10.) Hettne KM, de Mos M, de Bruijn AG, Weeber M, Boyer S, van Mulligen EM, et al. Applied information retrieval and multidisciplinary research: new mechanistic hypotheses in complex regional pain syndrome. J Biomed Discov Collab 2007;2:2.

(11.) Jinkins JR, Whittemore AR, Bradley WG. The anatomic basis of vertebrogenic pain and the autonomic syndrome associated with lumbar disk extrusion. AJR Am J Roentgenol 1989;152:1277-89.

(12.) Leis S, Weber M, Schmelz M, Birklein F. Facilitated neurogenic inflammation in unaffected limbs of patients with complex regional pain syndrome. Neurosci Lett 2004; 359:163-6.

(13.) Merritt WH. The challenge to manage reflex sympathetic dystrophy/complex regional pain syndrome. Clin Plast Surg 2005;32:575-604.

(14.) Sintzoff S, Sintzoff S Jr, Stallenberg B, Matos C. Imaging in reflex sympathetic dystrophy. Hand Clin 1997;13:431-42.

(15.) Seale KS. Reflex sympathetic dystrophy of the lower extremity. Clin Orthop Relat Res 1989;243:80-5.

Necmettin YILDIZ, (1) Gonca ODEMIS GUNGEN, (1) Olga YAYLALI, (2) Fusun ARDIC (1)

(1.) Departments of Physical Medicine and Rehabilitation, (2.) Department of Nuclear Medicine Medical Faculty of Pamukkale University, Denizli, Turkey

Received: November 2, 2009 Accepted: December 1, 2009

Correspondence: Necmettin Yildiz, M.D. Pamukkale Universitesi Tip Fakultesi Fizik Tedavi ve Rehabilitasyon Anabilim Dali, 20070 Kinikli, Denizli, Turkey. Tel: +90 258 - 444 07 28 / 4996 e-mail: necmi74tr@hotmail.com

Presented at the 5th World Congress of the International Society of Physical and Rehabilitation Medicine, June 13-17, 2009, Istanbul, Turkey.

[c] 2011 Turkish League Against Rheumatism. All rights reserved.

Turk J Rheumatol 2011;26(1):66-70

doi: 10.5606/tjr.2011.011
COPYRIGHT 2011 Turkish League Against Rheumatism
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Title Annotation:Case Report
Author:Yildiz, Necmettin; Gungen, Gonca Odemis; Yaylali, Olga; Ardic, Fusun
Publication:Turkish Journal of Rheumatology
Article Type:Disease/Disorder overview
Date:Mar 1, 2011
Words:1879
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