No. 212 Intradiscal Steroid Injection to Treat Patients With Neuropathic Pain Due to Discogenic Low Back Pain. Aydemir Koray; Yavuz Ferdi; Taskaynatan Mehmet Ali (Gulhane Military Medical Academy, Taf Rehabilitation Center Department of PMR, Ankara, Turkey). Disclosure: None. Objectives: An objective of this study was to investigate the effectiveness of intradiscal steroid injection in the treatment of discogenic low back pain (DLBP) with neuropathic pain (NEP). Setting: Tertiary level hospital. Participants: A total of 18 patients with DLBP were enrolled and divided into two groups based on having NEP and not. Group 1 included 11 patients who had DLBP without NEP, and group 2 included 7 patients who had DLBP with NEP. Main Outcome Measures: Duration and intensity of LBP, the Quebec Back Pain Disability Scale [QBPDS], the daily sleep interference scale [DSIS], and a Leeds assessment of neuropathic symptoms and signs [LANSS] pain scale. Level of Evidence: Level 3 evidence. Results: The mean age of the 18 patients was 43.712.7 (range: 24-60) years. Of these patients 9 (50%) were male. In our study 38.8% of the patients had DLBP with NEP, whereas 61.2% had mainly nociceptive pain. As we investigated the mean changes of the QBPDS scores and intensity of LBP in patients with a LANSS score 12 a statistically signicant reduction was found at the second week and third month after the treatment compared to pre-injection values (p<0.05). The mean reduction in the intensity of DLBP the QBPDS scores and the DSIS scores from baseline to second week and third month after the treatment was greater in group 2 than in group 1. However there was no signicant difference in the mean reduction of the outcome parameters between the two groups (p>0.05).
No. 213 Recurrent Complex Regional Pain Syndrome Type 1
With Bilateral Hand Involvement: A Case Report. Koray Aydemir; Volkan Yilmaz, MD; Taner Dandinoglu; Berke Aras (Gulhane Military Medical Academy, Department of Physical Medicine and Rehabilitation, Ankara, Turkey). Disclosure: None. Setting: Tertiary care university hospital. Patient: A 21-year-old male with bilateral upper extremity complex regional pain syndrome (CRPS) type-1. Case Description: The patient was admitted with complaints of swelling, sweating, and pain in both hands which had begun spontaneously. He had similar symptoms three years before and his complaints had healed spontaneously in 3 months. On physical examination the dorsum of both hands were cyanotic and swollen; the palmar sides of both hands were cold and damp. Widespread allodynia and hyperalgesia were noted. Periarticular osteoporosis of the hands were observed on x-ray. Magnetic resonance imaging (MRI) ndings in the carpal bones were compatible with CRPS. An arachnoid cyst in right cerebellar hemisphere and disorganization in the subcortical white matter in the right parietal lobe were detected in brain MRI. Functional brain MRI demonstrated an activity increase at the right parietal lobe. Slow theta waves were observed in electroencephalography. Results: After 8 weeks of physical therapy signicant improvements in hand function tests are noted. Discussion: CRPS is usually provoked by a trauma or surgery but a small proportion of patients develop CRPS without a clear causative event. The underlying mechanisms are not yet clearly understood. In this case report factors that might cause CRPS and cerebrocortical dysfunction in CRPS are discussed. Non-routine methods for brain processing during allodynia are also discussed. Conclusion: Bilateral recurrent CRPS is a very rare clinical condition. Parietal brain dysfunction may explain the central pain and allodynia in this case. Clinicians should consider central
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nerve system pathologies in evaluating idiopathic CRPS. Reprinted with
permission. No. 214 Klippel-Feil Syndrome: A Case Report. Koray Aydemir; Ismail Dede, MD; Ferdi Yavuz (Etimesgut Military Hospital, Department of Physical Medicine and Rehabilitation, Ankara, Turkey). Disclosure: None. Setting: Secondary care hospital. Patient: A 24year-old male with Klippel-Feil syndrome (KFS). Case Description: The patient presented to our clinic with neck and back pain with stiffness. His pain had started one year ago while working. Over time the pain had spread to the shoulders and the dorsal vertebrae. The pain was continuous and aggravating with standing and walking. On physical examination; he had facial asymmetry, torticollis, short neck, low hairline Sprengels deformity, and cervicothoracal scoliosis. Cervical spine range of motion (ROM) was decreased. Neurologic examination was normal. X-ray of the spine revealed fusion of the C5 and C6 vertebrae, interdiscal space narrowing at C2 and C3 levels, bilateral rudimental cervical costae, and cervicothoracal scoliosis. Ultrasound of the abdomen, echocardiogram, and audiometry were normal. Assessments/Results: Exercises for scoliosis, cervical spine strengthening/ROM are started and non-steroidal anti-inammatory medicine is prescribed. Modications in lifestyle are recommended. Improvements in pain and functionality are observed. Discussion: KFS is a rare disease characterized by the congenital fusion of any 2 of the cervical vertebrae. Clinical triad of the disease consists of short neck, low hairline, and decreased ROM of the cervical spine. Also systemic ndings like scoliosis, kyphosis, Sprengels deformity, torticollis, craniofacial asymmetry, renal and cardiac abnormalities, loss of hearing, and synkinesis may exist. Clinical characteristics and the differential diagnosis of the KFS will be discussed. Conclusion: Many of the people with KFS may be asymptomatic; symptoms of the disease may develop during time. These patients should be evaluated in terms of systemic pathologies. A multidisciplinary approach for treatment and management for the accompanying abnormalities is recommended. Reprinted with permission. No. 215 CRPS Type-2 as the Initial Clinical Manifestation of Iatrogenic Sciatic Nerve Injury After Total Hip Arthroplasty: A Case Report. Koray Aydemir; Umut Guzelkucuk Asst. Prof, MD; Serdar Kesikburun; Yasin Demir (Gulhane Military Medical Academy Department of Physical Medicine and Rehabilitation Turkish Armed Forces Rehabilitation Center, Ankara, Turkey). Disclosure: None. Setting: Tertiary care university hospital. Patient: A 59-year-old female with iatrogenic sciatic nerve injury (SNI) after total hip arthroplasty (THA). Case Description: The patient presented to our clinic with complaints of severe pain, swelling, and sweating at her left foot. She had a unilateral THA for congenital hip subluxation 2 weeks before. Severe pain had started on her left foot one week after the surgery. Electromyogram (EMG), feet x-ray, and magnetic resonance imaging were normal. She was inspected by dermatology and cardiovascular surgery clinics but a specic disease could not be found. On physical examination; allodynia, hyperalgesia, hyperemia, swelling and a non-dermatomal hypoesthesia on left foot were observed. Manual muscle testing was unreliable due to the severe pain in left hip and left foot. 3-phase bone scan was consistent with early period CRPS. With these clinical and scintigraphic ndings, the patient was considered as CRPS and physical medicine and rehabilitation programme is started. The EMG which was performed one month after the surgery demonstrated a partial axonal degeneration on the peroneal and total axonal degeneration on the tibial branches of the sciatic nerve. Discussion: Femoral nerve and more commonly sciatic nerve injuries are one of the most serious complications of the THA. CRPS type-2