Superior cluneal nerves

Last updated
Superior cluneal nerves
Gray826and831.PNG
Cutaneous nerves of the right lower extremity. Front and posterior views. (Posterior division of lumbar visible in yellow at top right.)
Details
From dorsal rami of L1-L3 nerve roots
Innervatesupper buttocks
Identifiers
Latin nervi clunium superiores
TA98 A14.2.05.006
TA2 6493
FMA 75468
Anatomical terms of neuroanatomy

The superior cluneal nerves are pure sensory nerves that innervate the skin of the upper part of the buttocks. They are the terminal ends of the L1-L3 spinal nerve dorsal rami lateral branches. They are one of three different types of cluneal nerves (the middle and inferior cluneal nerves being the other two). They travel inferiorly through multiple layers of muscles, then traverse osteofibrous tunnels between the thoracolumbar fascia and iliac crest. [1]

Contents

Dysfunction of the superior cluneal nerves is often due to entrapment as the nerves cross the iliac crest – this can result in numbness, tingling or pain in the low back and upper buttocks region. Superior cluneal nerve dysfunction is a clinical diagnosis that can be supported by diagnostic nerve blocks. [1]

The superior cluneal nerves were first described by Maigne et al. in 1989 as a source of low back pain. [2]

Anatomy

Origin

These nerves are grouped as the superior cluneal nerves due to their trajectory over the iliac spine, as opposed to the lateral, medial and inferior cluneal nerves. These nerves most commonly originate from the dorsal rami of the L1, L2, and L3 nerve roots. In cadaver studies, a small percentage of patients will also have origins at the L4 and L5 nerve roots. [3] [4]

Course and relations

After they branch off the dorsal rami, they pass through the erector spinae muscle, psoas major, paraspinal muscles, and then inferior latissimus dorsi to reach the iliac crest. [5]

The nerves then pass through an osteofibrous tunnel created by the thoracolumbar fascia and rim of the superior iliac crest. [6] Cadaver studies have noted that some patients have boney grooves along the rim that house the superior cluneal nerves. On average, these grooves are found between 5–7 cm from the midline. [7] [8] These grooves can often be visualized with an ultrasound. [8]

The nerves terminate over the gluteal fascia distal to the iliac crest.[ citation needed ]

Clinical significance

Damage to the cluneal nerves can be from direct injury or from entrapment between the muscles or in the osteofibrous tunnel. Direct injury to the cluneal nerves can happen during posterior iliac crest harvest to obtain bone mineral for other surgeries, such as spinal arthrodesis. [9] [10] Entrapment of the nerve can occur at any point but is most common across the osteofibrous tunnel.[ citation needed ]

Superior cluneal nerve dysfunction

Dysfunction of the superior cluneal nerves lead to many different neuropathic symptoms such as burning pain, numbness, tingling, and dysesthesia around the low back and upper gluteal area. The most common symptoms are localized unilateral low back pain, though up to anywhere between 40 and 82% of patients may complain of leg symptoms – pain or dysethesia. [5] [11] [12] The onset of pain can vary, with some patients report sudden onset of pain with a known inciting incident. [13] These symptoms can be exacerbated by lumbar flexion, extension, and rotation. [1] Manual compression over the posterior superior iliac crest, such as with wearing tight clothing and belts, can also reproduce symptoms. [1] [5] Many patients also have tender points located around the posterior iliac crest, approximately 7 cm from midline which correlates with cadaver studies demonstrating the location at which the nerves cross the iliac crest. [5] [14] On physical exam, the pain can be reproduced by the excessive motions listed above or by tapping along the posterior superior iliac crest, which would be a positive Tinel-like sign. [5] [14] In the setting of nerve entrapment between the muscles, activation of the muscles with lumbar extension can reproduce the pain. [5] Besides pain, patients can also have reduced sensation to light touch over the nerve distribution. [1] [5] [14]

Diagnosis of superior cluneal nerve dysfunction requires the help of a skilled clinician as it requires a good history and physical examination. Imaging, such as magnetic resonance imaging, can be used to rule out other pathologies. In many cases, this diagnosis is made after treatment of more common pathologies with similar symptoms. The most common overlapping pathologies include facet joint pain, sacroiliac joint dysfunction, and lumbosacral radiculopathy. Electrodiagnostic studies, including electromyography and nerve conduction studies, can also help rule out other pathologies. [1] Currently, there is no consistent protocol for testing the superior cluneal nerves with a nerve conduction study. Diagnosis of superior cluneal nerve entrapment can be aided by diagnostic blocks of the nerve across the iliac crest. [1] [5]

Treatment

The treatment for superior cluneal nerve dysfunction can vary based on the clinician and severity of symptoms. There is currently limited evidence for treatment at this time. Physical therapy can be initiated to improve strength and flexibility. The addition of non-steroidal anti-inflammatory medications can help with overall discomfort but has not been shown to have direct effects of the nerve. Specifically, the use of COX-2 inhibitors is a reasonable first step. [1] Other treatments of superior cluneal nerve dysfunction include both minimally invasive interventions and surgical options. Minimally invasive treatments include nerve blocks, neuroablation, and neuromodulation. [5] Efficacy of these interventions are still being studied and no clear evidence to show long term benefits in larger studies. Minimally invasive treatments can be performed with ultrasound or fluoroscopy to improve safety and accuracy.

Nerve blocks are injections that target specific nerves to serve as both therapeutic and diagnostic purposes. They have been used for a variety of neuropathic conditions including facet joint pain. Nerve block injections specifically targeted at the superior cluneal nerves are limited. [5] However, these blocks are minimally invasive and involve injecting medications at the nerves as they cross the iliac crest. [11] These blocks can be done with local anesthetics with or without corticosteroids. [1] [5] [11] Improvement in pain after these blocks suggest that these nerves are the source of the patient's symptoms, however these blocks are often temporary and studies regarding corticosteroid reported 68% of patients had improved back pain after 1-3 repetitive blocks. [11] These injections can be performed with or without image modalities, though the use of ultrasound guidance may help optimize medication delivery [11] [8] [15] These procedures can also be done under fluoroscopy.

Neuroablation can be performed with chemical neurolysis or radiofrequency ablation. These techniques are often used on the medial branch nerves to treat low back pain and have been applied to the superior cluneal nerves. The use of phenol has been noted to relieve pain for up to 9 months but may not completely resolve symptoms. [5]

Neuromodulation of the cluneal nerve with peripheral nerve stimulation has not been widely established as an effective treatment, though there are some studies that show significant benefits. [5] [16]

Surgical intervention typically involves decompression of the nerves from the osteofibrous tunnels. Few studies have shown long term benefits of surgical intervention. [17] [18]

Additional images

Related Research Articles

Pudendal nerve entrapment (PNE), also known as Alcock canal syndrome, is an uncommon source of chronic pain in which the pudendal nerve is entrapped or compressed in Alcock's canal. There are several different types of PNE based on the site of entrapment anatomically. Pain is positional and is worsened by sitting. Other symptoms include genital numbness, fecal incontinence and urinary incontinence.

<span class="mw-page-title-main">Sacroiliac joint</span> Joint of the pelvis and spine

The sacroiliac joint or SI joint (SIJ) is the joint between the sacrum and the ilium bones of the pelvis, which are connected by strong ligaments. In humans, the sacrum supports the spine and is supported in turn by an ilium on each side. The joint is strong, supporting the entire weight of the upper body. It is a synovial plane joint with irregular elevations and depressions that produce interlocking of the two bones. The human body has two sacroiliac joints, one on the left and one on the right, that often match each other but are highly variable from person to person.

<span class="mw-page-title-main">Piriformis syndrome</span> Medical condition

Piriformis syndrome is a condition which is believed to result from compression of the sciatic nerve by the piriformis muscle. The largest and most bulky nerve in the human body is the sciatic nerve. Starting at its origin it is 2 cm wide and 0.5 cm thick. The sciatic nerve forms the roots of L4-S3 segments of the lumbosacral plexus. The nerve will pass inferiorly to the piriformis muscle, in the direction of the lower limb where it divides into common tibial and fibular nerves. Symptoms may include pain and numbness in the buttocks and down the leg. Often symptoms are worsened with sitting or running.

Occipital neuralgia (ON) is a painful condition affecting the posterior head in the distributions of the greater occipital nerve (GON), lesser occipital nerve (LON), third occipital nerve (TON), or a combination of the three. It is paroxysmal, lasting from seconds to minutes, and often consists of lancinating pain that directly results from the pathology of one of these nerves. It is paramount that physicians understand the differential diagnosis for this condition and specific diagnostic criteria. There are multiple treatment modalities, several of which have well-established efficacy in treating this condition.

<span class="mw-page-title-main">Pterygopalatine ganglion</span> Parasympathetic ganglion in the pterygopalatine fossa

The pterygopalatine ganglion is a parasympathetic ganglion in the pterygopalatine fossa. It is one of four parasympathetic ganglia of the head and neck,.

<span class="mw-page-title-main">Tarsal tunnel syndrome</span> Medical condition

Tarsal tunnel syndrome (TTS) is a nerve entrapment syndrome causing a painful foot condition in which the tibial nerve is compressed as it travels through the tarsal tunnel. This tunnel is found along the inner leg behind the medial malleolus. The posterior tibial artery, tibial nerve, and tendons of the tibialis posterior, flexor digitorum longus, and flexor hallucis longus muscles travel in a bundle through the tarsal tunnel. Inside the tunnel, the nerve splits into three segments. One nerve (calcaneal) continues to the heel, the other two continue on to the bottom of the foot. The tarsal tunnel is delineated by bone on the inside and the flexor retinaculum on the outside.

<span class="mw-page-title-main">Nerve block</span> Deliberate inhibition of nerve impulses

Nerve block or regional nerve blockade is any deliberate interruption of signals traveling along a nerve, often for the purpose of pain relief. Local anesthetic nerve block is a short-term block, usually lasting hours or days, involving the injection of an anesthetic, a corticosteroid, and other agents onto or near a nerve. Neurolytic block, the deliberate temporary degeneration of nerve fibers through the application of chemicals, heat, or freezing, produces a block that may persist for weeks, months, or indefinitely. Neurectomy, the cutting through or removal of a nerve or a section of a nerve, usually produces a permanent block. Because neurectomy of a sensory nerve is often followed, months later, by the emergence of new, more intense pain, sensory nerve neurectomy is rarely performed.

<span class="mw-page-title-main">Morton's neuroma</span> Benign neuroma of an intermetatarsal plantar nerve

Morton's neuroma is a benign neuroma of an intermetatarsal plantar nerve, most commonly of the second and third intermetatarsal spaces, which results in the entrapment of the affected nerve. The main symptoms are pain and/or numbness, sometimes relieved by ceasing to wear footwear with tight toe boxes and high heels. The condition is named after Thomas George Morton, though it was first correctly described by a chiropodist named Durlacher.

<span class="mw-page-title-main">Lateral cutaneous nerve of thigh</span> Nerve of the thigh

The lateral cutaneous nerve of the thigh is a cutaneous nerve of the thigh. It originates from the dorsal divisions of the second and third lumbar nerves from of lumbar plexus. It passes under the inguinal ligament to reach the thigh. It supplies sensation to the skin on the lateral part of the thigh by an anterior branch and a posterior branch.

Percutaneous tibial nerve stimulation (PTNS), also referred to as posterior tibial nerve stimulation, is the least invasive form of neuromodulation used to treat overactive bladder (OAB) and the associated symptoms of urinary urgency, urinary frequency and urge incontinence. These urinary symptoms may also occur with interstitial cystitis and following a radical prostatectomy. Outside the United States, PTNS is also used to treat fecal incontinence.

Sacral nerve stimulation, also termed sacral neuromodulation, is a type of medical electrical stimulation therapy.

<span class="mw-page-title-main">Denervation</span> Loss of nerve supply

Denervation is any loss of nerve supply regardless of the cause. If the nerves lost to denervation are part of the neuronal communication to a specific function in the body then altered or a loss of physiological functioning can occur. Denervation can be caused by injury or be a symptom of a disorder like ALS, post-polio syndrome, or POTS. Additionally, it can be a useful surgical technique to alleviate major negative symptoms, such as in renal denervation. Denervation can have many harmful side effects such as increased risk of infection and tissue dysfunction.

<span class="mw-page-title-main">Nerve compression syndrome</span> Human disease

Nerve compression syndrome, or compression neuropathy, or nerve entrapment syndrome, is a medical condition caused by chronic, direct pressure on a peripheral nerve. It is known colloquially as a trapped nerve, though this may also refer to nerve root compression. Its symptoms include pain, tingling, numbness and muscle weakness. The symptoms affect just one particular part of the body, depending on which nerve is affected. The diagnosis is largely clinical and can be confirmed with diagnostic nerve blocks. Occasionally imaging and electrophysiology studies aid in the diagnosis. Timely diagnosis is important as untreated chronic nerve compression may cause permanent damage. A surgical nerve decompression can relieve pressure on the nerve but cannot always reverse the physiological changes that occurred before treatment. Nerve injury by a single episode of physical trauma is in one sense an acute compression neuropathy but is not usually included under this heading, as chronic compression takes a unique pathophysiological course.

<span class="mw-page-title-main">Spinal stenosis</span> Disease of the bony spine that results in narrowing of the spinal canal

Spinal stenosis is an abnormal narrowing of the spinal canal or neural foramen that results in pressure on the spinal cord or nerve roots. Symptoms may include pain, numbness, or weakness in the arms or legs. Symptoms are typically gradual in onset and improve with leaning forward. Severe symptoms may include loss of bladder control, loss of bowel control, or sexual dysfunction.

<span class="mw-page-title-main">Sacroiliac joint dysfunction</span> Medical condition

The term sacroiliac joint dysfunction refers to abnormal motion in the sacroiliac joint, either too much motion or too little motion, that causes pain in this region.

<span class="mw-page-title-main">Intercostal nerve block</span> Procedure for pain relief

Intercostal nerve block is a nerve block which temporarily or permanently interrupts the flow of signals along an intercostal nerve, usually performed to relieve pain.

Anterior cutaneous nerve entrapment syndrome (ACNES) is a nerve entrapment condition that causes chronic pain of the abdominal wall. It occurs when nerve endings of the lower thoracic intercostal nerves (7–12) are 'entrapped' in abdominal muscles, causing a severe localized nerve (neuropathic) pain that is usually experienced at the front of the abdomen.

Femoral nerve dysfunction, also known as femoral neuropathy, is a rare type of peripheral nervous system disorder that arises from damage to nerves, specifically the femoral nerve. Given the location of the femoral nerve, indications of dysfunction are centered around the lack of mobility and sensation in lower parts of the legs. The causes of such neuropathy can stem from both direct and indirect injuries, pressures and diseases. Physical examinations are usually first carried out, depending on the high severity of the injury. In the cases of patients with hemorrhage, imaging techniques are used before any physical examination. Another diagnostic method, electrodiagnostic studies, are recognized as the gold standard that is used to confirm the injury of the femoral nerve. After diagnosis, different treatment methods are provided to the patients depending upon their symptoms in order to effectively target the underlying causes. Currently, femoral neuropathy is highly underdiagnosed and its precedent medical history is not well documented worldwide.

<span class="mw-page-title-main">Iliocostal friction syndrome</span> Medical condition

Iliocostal friction syndrome, also known as costoiliac impingement syndrome, is a condition in which the costal margin comes in contact with the iliac crest. The condition presents as low back pain which may radiate to other surrounding areas as a result of irritated nerve, tendon, and muscle structures. It may occur unilaterally due to conditions such as scoliosis, or bilaterally due to conditions such as osteoporosis and hyperkyphosis.

Nerve glide, also known as nerve flossing or nerve stretching, is an exercise that stretches nerves. It facilitates the smooth and regular movement of peripheral nerves in the body. It allows the nerve to glide freely along with the movement of the joint and relax the nerve from compression. Nerve gliding cannot proceed with injuries or inflammations as the nerve is trapped by the tissue surrounding the nerve near the joint. Thus, nerve gliding exercise is widely used in rehabilitation programs and during the post-surgical period. In addition to rehabilitating purposes, nerve gliding exercise is also used alongside other treatments to relieve the symptoms and faster recovery.

References

  1. 1 2 3 4 5 6 7 8 9 Waldman SD. Atlas of Uncommon Pain Syndromes. 3rd ed. Philadelphia, PA: Saunders/Elsevier; 2014.
  2. Maigne, J. Y.; Lazareth, J. P.; Surville, H. Guérin; Maigne, R. (1989). "The lateral cutaneous branches of the dorsal rami of the thoraco-lumbar junction". Surgical and Radiologic Anatomy. 11 (4): 289–293. doi:10.1007/BF02098698. PMID   2533408. S2CID   39158958.
  3. Iwanaga, Joe; Simonds, Emily; Schumacher, Maia; Oskouian, Rod J.; Tubbs, R. Shane (2019). "Anatomic Study of Superior Cluneal Nerves: Revisiting the Contribution of Lumbar Spinal Nerves". World Neurosurgery. 128: e12–e15. doi:10.1016/j.wneu.2019.02.159. PMID   30862587. S2CID   76663848.
  4. Konno, Tomoyuki; Aota, Yoichi; Kuniya, Hiroshi; Saito, Tomoyuki; Qu, Ning; Hayashi, Shogo; Kawata, Shinichi; Itoh, Masahiro (2017). "Anatomical etiology of "pseudo-sciatica" from superior cluneal nerve entrapment: A laboratory investigation". Journal of Pain Research. 10: 2539–2545. doi: 10.2147/jpr.s142115 . PMC   5677392 . PMID   29138591.
  5. 1 2 3 4 5 6 7 8 9 10 11 12 13 Karri, Jay; Singh, Mani; Orhurhu, Vwaire; Joshi, Mihir; Abd-Elsayed, Alaa (2020). "Pain Syndromes Secondary to Cluneal Nerve Entrapment". Current Pain and Headache Reports. 24 (10): 61. doi:10.1007/s11916-020-00891-7. PMID   32821979. S2CID   221199448.
  6. Lu, J.; Ebraheim, N. A.; Huntoon, M.; Heck, B. E.; Yeasting, R. A. (1998). "Anatomic considerations of superior cluneal nerve at posterior iliac crest region". Clinical Orthopaedics and Related Research (347): 224–228. PMID   9520894.
  7. Iwanaga, Joe; Simonds, Emily; Schumacher, Maia; Yilmaz, Emre; Altafulla, Juan; Tubbs, R. Shane (2019). "Anatomic Study of the Superior Cluneal Nerve and Its Related Groove on the Iliac Crest". World Neurosurgery. 125: e925–e928. doi:10.1016/j.wneu.2019.01.210. PMID   30763748. S2CID   73430020.
  8. 1 2 3 Fan, Kun; Cheng, Chen; Gong, Wen-Yi (2021). "A simple and novel ultrasound-guided approach for superior cluneal nerves block". Anaesthesia Critical Care & Pain Medicine. 40 (2): 100838. doi:10.1016/j.accpm.2021.100838. PMID   33757913. S2CID   232337450.
  9. Ebraheim, Nabil A.; Elgafy, Hossein; Xu, Rongming (2001). "Bone-Graft Harvesting from Iliac and Fibular Donor Sites: Techniques and Complications". Journal of the American Academy of Orthopaedic Surgeons. 9 (3): 210–218. doi:10.5435/00124635-200105000-00007. PMID   11421578. S2CID   24103745.
  10. Tubbs, R. Shane; Levin, Matthew R.; Loukas, Marios; Potts, Eric A.; Cohen-Gadol, Aaron A. (2010). "Anatomy and landmarks for the superior and middle cluneal nerves: Application to posterior iliac crest harvest and entrapment syndromes". Journal of Neurosurgery: Spine. 13 (3): 356–359. doi: 10.3171/2010.3.spine09747 . PMID   20809730.
  11. 1 2 3 4 5 Kuniya, Hiroshi; Aota, Yoichi; Kawai, Takuya; Kaneko, Kan-Ichiro; Konno, Tomoyuki; Saito, Tomoyuki (2014). "Prospective study of superior cluneal nerve disorder as a potential cause of low back pain and leg symptoms". Journal of Orthopaedic Surgery and Research. 9: 139. doi: 10.1186/s13018-014-0139-7 . PMC   4299373 . PMID   25551470.
  12. Miki, Koichi; Kim, Kyongsong; Isu, Toyohiko; Matsumoto, Juntaro; Kokubo, Rinko; Isobe, Masanori; Inoue, Tooru (2019). "Characteristics of Low Back Pain due to Superior Cluneal Nerve Entrapment Neuropathy". Asian Spine Journal. 13 (5): 772–778. doi:10.31616/asj.2018.0324. PMC   6773996 . PMID   31079427.
  13. Kim, Kyongsong; Isu, Toyohiko; Chiba, Yasuhiro; Iwamoto, Naotaka; Yamazaki, Kazuyoshi; Morimoto, Daijiro; Isobe, Masanori; Inoue, Kiyoharu (2015). "Treatment of low back pain in patients with vertebral compression fractures and superior cluneal nerve entrapment neuropathies". Surgical Neurology International. 6 (25): S619-21. doi: 10.4103/2152-7806.170455 . PMC   4671138 . PMID   26693392.
  14. 1 2 3 Isu, Toyohiko; Kim, Kyongsong; Morimoto, Daijiro; Iwamoto, Naotaka (2018). "Superior and Middle Cluneal Nerve Entrapment as a Cause of Low Back Pain". Neurospine. 15 (1): 25–32. doi: 10.14245/ns.1836024.012 . PMC   5944640 . PMID   29656623. S2CID   4899042.
  15. Nielsen, Thomas Dahl; Moriggl, Bernhard; Barckman, Jeppe; Jensen, Jan Mick; Kolsen-Petersen, Jens Aage; Søballe, Kjeld; Børglum, Jens; Bendtsen, Thomas Fichtner (2019). "Randomized trial of ultrasound-guided superior cluneal nerve block". Regional Anesthesia & Pain Medicine. 44 (8): 772–780. doi:10.1136/rapm-2018-100174. PMID   31061111. S2CID   146810542.
  16. Deer, Timothy; Pope, Jason; Benyamin, Ramsin; Vallejo, Ricardo; Friedman, Andrew; Caraway, David; Staats, Peter; Grigsby, Eric; Porter Mcroberts, W.; McJunkin, Tory; Shubin, Richard; Vahedifar, Payam; Tavanaiepour, Daryoush; Levy, Robert; Kapural, Leonardo; Mekhail, Nagy (2016). "Prospective, Multicenter, Randomized, Double-Blinded, Partial Crossover Study to Assess the Safety and Efficacy of the Novel Neuromodulation System in the Treatment of Patients with Chronic Pain of Peripheral Nerve Origin". Neuromodulation: Technology at the Neural Interface. 19 (1): 91–100. doi:10.1111/ner.12381. PMID   26799373. S2CID   23413856.
  17. Maigne, Jean-Yves; Doursounian, Levon (1997). "Entrapment Neuropathy of the Medial Superior Cluneal Nerve". Spine. 22 (10): 1156–1159. doi:10.1097/00007632-199705150-00017. PMID   9160476. S2CID   40323409.
  18. Morimoto, Daijiro; Isu, Toyohiko; Kim, Kyongsong; Chiba, Yasuhiro; Iwamoto, Naotaka; Isobe, Masanori; Morita, Akio (2017). "Long-term Outcome of Surgical Treatment for Superior Cluneal Nerve Entrapment Neuropathy". Spine. 42 (10): 783–788. doi:10.1097/brs.0000000000001913. PMID   27669049. S2CID   4383288.