0
Observation | ONLINE FIRST

Scalp Dysesthesia Related to Cervical Spine Disease FREE

Laura A. Thornsberry, MD; Joseph C. English III, MD
[+] Author Affiliations

Author Affiliations: Department of Dermatology, University of Pittsburgh, Pittsburgh, Pennsylvania.


JAMA Dermatol. 2013;149(2):200-203. doi:10.1001/jamadermatol.2013.914.
Text Size: A A A
Published online

Background Scalp dysesthesia is characterized by abnormal sensations of the scalp in the absence of any other unusual physical examination findings. The pathogenesis of this condition is unknown but has been reported in the setting of underlying psychiatric disorders. Other localized pruritic syndromes, including brachioradial pruritus and notalgia paresthetica, have been associated with pathologic conditions of the spine and have been successfully treated with gabapentin.

Observations Among 15 women identified in a retrospective review of medical records as having been seen with scalp dysesthesia, 14 patients had cervical spine disease confirmed by imaging. The most common finding on imaging was degenerative disk disease, with 10 of 14 patients having these changes at C5-C6. Other abnormal imaging findings included anterolisthesis, osteophytic spurring, lordosis, kyphosis, and nerve root impingement. A gabapentin regimen (topical or oral) had been recommended to 14 patients; of 7 patients who were followed up, 4 patients noted improvement in symptoms when taking gabapentin.

Conclusions Patients with scalp dysesthesia also had abnormal cervical spine images. Chronic muscle tension placed on the pericranial muscles and scalp aponeurosis secondary to the underlying cervical spine disease may lead to the symptoms of scalp dysesthesia.

Scalp dysesthesia was first described by Hoss and Segal1 in 1998 as a cutaneous dysesthesia syndrome characterized by pruritus, burning, stinging, or pain of the scalp in the absence of any other unusual physical examination findings. In their case series of 11 patients, 5 patients had at least 1 known psychiatric disorder (dysthymic disorder, somatization disorder, or generalized anxiety disorder), 7 patients had symptoms worsened by stress, and 9 patients had symptom improvement with low-dose antidepressant treatment.1 Their study did not examine underlying cervical spine disease among the patients. The pathogenesis of scalp dysesthesia is poorly understood and has not been determined.

Other localized pruritic syndromes, including brachioradial pruritus and notalgia paresthetica, have been associated with pathologic conditions of the spine confirmed by cervical and thoracic spine imaging studies.25 In a study2 of 41 patients with brachioradial pruritus, 29 patients had abnormal magnetic resonance (MR) images showing nerve compression correlating with the dermatomal distribution of the pruritus. A case series3 of 10 patients with notalgia paresthetica showed a relationship between the location of the symptoms and the abnormal images in 7 patients. The radiologic findings in brachioradial pruritus and notalgia paresthetica prompted our study of cervical spine imaging in patients seen with scalp dysesthesia.

In our patients (Table), the most common symptoms of scalp dysesthesia were burning (7 patients), pruritus (6 patients), or both burning and pruritus (2 patients). Two patients described a sensation of “bugs crawling” on the scalp. Two patients had concurrent chronic telogen effluvium, and 2 other patients reported subjective hair loss that was not further described in the medical records. Two patients reported chronic neck pain, and 1 patient had a history of a C6-C7 fusion surgical procedure. None of the patients had worsening or improvement of the symptoms with certain head positions or exercises. The symptoms were diffuse in 10 patients and were localized to various regions of the scalp in 5 patients, including the frontal, vertex, occipital, parietal, and temporal scalp. One patient with diffuse scalp burning also reported burning in the right arm. The duration of symptoms before presentation ranged from several months to 8 years. All 15 patients were women of white race/ethnicity, with an age range of 38 to 83 years. Two patients had a diagnosis of depression, and 1 patient had a history of anxiety. None of the patients indicated that stress had any influence on their symptoms. The physical examinations were unremarkable for primary lesions, although 3 patients had secondary excoriations in the symptomatic areas of their scalps. The differential diagnosis for scalp pruritus includes many common dermatologic conditions, including seborrheic dermatitis, psoriasis, scarring alopecia, tinea capitis, pediculosis, contact dermatitis, allergic dermatitis, acne, and folliculitis. The physical examination has a crucial role in the diagnosis of many of these conditions, and a key component to diagnosing scalp dysesthesia is the lack of objective primary skin findings.

Table Graphic Jump LocationTable. Patients With Scalp Dysesthesia and Cervical Spine Imaging

In this retrospective study, 14 of 15 patients had abnormal findings visualized on cervical spine radiographs, MR imaging, or computed tomography. The most common radiographic abnormality was degenerative disk disease (DDD), which was present in 11 patients and occurred at C5-C6 in 10 patients. Five patients had DDD only at level C5-C6, while 6 patients had multilevel disease. Two patients had DDD at C4-C7, 2 patients had DDD at C5-C7, 1 patient had DDD at C4-C6, and 1 patient had DDD at C6-C7. Other pertinent radiographic findings included grade 1 anterolisthesis, osteophytic spurring, lordosis, kyphosis, and nerve root impingement. One patient had both a normal cervical spine radiograph and normal MR images.

Gabapentin, as a topical or an oral medication, had been recommended as a treatment option to 14 patients. Only 7 of these patients returned for follow-up appointments after using gabapentin, with 4 patients reporting an improvement in symptoms. Two patients improved when taking oral gabapentin (100 mg 3 times daily), while 2 patients had improvement with topical gabapentin, 10%, cream (3 applications daily). The topical cream was compounded using gabapentin powder and a lipophilic liposomic base, with propylene glycol as the wetting agent. Three patients reported no improvement with gabapentin. One patient had to discontinue oral gabapentin secondary to palpitations. Three patients reported some improvement with topical corticosteroids (clobetasol propionate and hydrocortisone). Three patients received low-dose antidepressants. One patient tried venlafaxine hydrochloride (18.75 mg/d) plus gabapentin (100 mg twice daily), with no improvement in symptoms. A second patient had a partial response with venlafaxine hydrochloride (50 mg/d) and topical gabapentin, 10% (3 times daily). The third patient tried amitriptyline hydrochloride (25 mg/d) without any other medications, with a partial response. Nonpharmacologic treatments had also been recommended. Two patients completed neck physical therapy, with no mention of any improvement in symptoms. One patient was referred to a chiropractor but did not follow up after the recommendation. Seven patients were referred to a neurologist, but only 1 patient had the medical records available for review, which included a normal electromyogram and unremarkable findings in a nerve conduction study of the right upper arm; she had also reported right arm burning.

In this study of 15 women identified in a retrospective review of medical records as having been seen with scalp dysesthesia, 14 patients had cervical spine disease confirmed by imaging. We suggest an association between scalp dysesthesia and cervical spine disease, most commonly DDD. Scalp dysesthesia does not seem to follow a dermatomal distribution given that the most common location of DDD in our study was C5-C6. We hypothesize that the symptoms of scalp dysesthesia may be related to chronic tension placed on the occipitofrontalis muscle and scalp aponeurosis (galea aponeurotica) secondary to underlying cervical spine disease, rather than psychiatric causes. This parallels the pathogenesis of a tension-type headache, which is thought to have a musculoskeletal component related to chronic tension of the pericranial muscles and myofascial pain.6 The pain of a tension headache can be diffuse or localized; similarly, the location of the symptoms of scalp dysesthesia was variable in this study, with 10 patients having diffuse symptoms and 5 patients reporting specific areas of concern on the scalp. The cause of this variability is unknown.

Degenerative changes of the cervical spine are known to linearly increase with age.7 In a study7 of 497 asymptomatic patients, MR imaging of the cervical spine showed degenerative changes in 12% of women in their 20s and in 89% of women older than 60 years. In our study, the percentage of women with abnormal images was 93% (14 of 15 patients), which is higher than that among the asymptomatic population, and covered a wide age range of 38 to 83 years.

Scalp dysesthesia can be a challenging and frustrating condition for the patient and the physician because it does not have well-established or evidence-based treatments, with low-dose antidepressants as the only reported treatment to date.1 Gabapentin has been approved by the Food and Drug Administration for partial seizures and postherpetic neuralgia; however, it has been reported as an effective treatment of neuropathic pain and refractory pruritus of unknown origin.8,9 Several case reports8,1012document the successful use of gabapentin at varying dosages (range, 100 mg 3 times daily to 300 mg every 4 hours) for brachioradial pruritus. Although the mechanism of action of gabapentin is unknown, it affects neurotransmitters; specifically, it inhibits glutamate synthesis and increases the transmission of γ-aminobutyric acid.8 Gabapentin is generally well tolerated, with common adverse effects of dizziness, drowsiness, and lower extremity edema.

Gabapentin (topical or oral) was the most commonly prescribed medication in this study. Four patients showed improvement with gabapentin treatment, while 3 patients did not, demonstrating that gabapentin may be an effective treatment of scalp dysesthesia but will require larger studies in the future. Other treatments included low-dose antidepressants, including venlafaxine and amitriptyline; however, venlafaxine was used in combination with gabapentin, preventing the evaluation of the individual effect of each drug.

The outcomes of the treatments used in this study were limited by the absence of patient follow-up data for 7 patients who did not return for their appointments. These patients had been initially seen at a tertiary care center, to which patients frequently drive 4 to 6 hours for appointments, which likely contributed to the poor follow-up response because patients may have chosen a location closer to home for their continued care.

In conclusion, scalp dysesthesia is a syndrome characterized primarily by scalp burning or pruritus in the absence of any other unusual physical examination findings and may be associated with cervical spine disease. In this study, 14 of 15 of patients with scalp dysesthesia also had abnormal cervical spine images. The pathogenesis may be related to chronic muscle tension placed on the pericranial muscles and scalp aponeurosis secondary to the underlying cervical spine disease and is likely unrelated to psychiatric disorders. Four patients reported improvement in symptoms with gabapentin, but the optimal dosage and route of administration need to be studied. Larger, prospective studies are needed to further characterize the pathogenesis of scalp dysesthesia and to determine the most efficacious treatments.

Correspondence: Joseph C. English III, MD, Department of Dermatology, University of Pittsburgh, 200 Lothrop St, Ste 3880, Presby South Tower, Pittsburgh, PA 15213 (englishjc@upmc.edu).

Accepted for Publication: August 28, 2012.

Published Online: November 19, 2012. doi:10.1001/jamadermatol.2013.914

Author Contributions: Drs Thornsberry and English had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: English. Acquisition of data: Thornsberry and English. Analysis and interpretation of data: Thornsberry and English. Drafting of the manuscript: Thornsberry. Critical revision of the manuscript for important intellectual content: English. Administrative, technical, and material support: English. Study supervision: English.

Conflict of Interest Disclosures: None reported.

Hoss D, Segal S. Scalp dysesthesia.  Arch Dermatol. 1998;134(3):327-330
PubMed   |  Link to Article
Marziniak M, Phan NQ, Raap U,  et al.  Brachioradial pruritus as a result of cervical spine pathology: the results of a magnetic resonance tomography study.  J Am Acad Dermatol. 2011;65(4):756-762
PubMed   |  Link to Article
Savk E, Savk O, Bolukbasi O,  et al.  Notalgia paresthetica: a study on pathogenesis.  Int J Dermatol. 2000;39(10):754-759
PubMed   |  Link to Article
Raison-Peyron N, Meunier L, Acevedo M, Meynadier J. Notalgia paresthetica: clinical, physiopathological and therapeutic aspects: a study of 12 cases.  J Eur Acad Dermatol Venereol. 1999;12(3):215-221
PubMed   |  Link to Article
Alai NN, Skinner HB, Nabili ST, Jeffes E, Shahrokni S, Saemi AM. Notalgia paresthetica associated with cervical spinal stenosis and cervicothoracic disk disease at C4 through C7.  Cutis. 2010;85(2):77-81
PubMed
Fumal A, Schoenen J. Tension-type headache: current research and clinical management.  Lancet Neurol. 2008;7(1):70-83
PubMed   |  Link to Article
Matsumoto M, Fujimura Y, Suzuki N,  et al.  MRI of cervical intervertebral discs in asymptomatic subjects.  J Bone Joint Surg Br. 1998;80(1):19-24
PubMed   |  Link to Article
Scheinfeld N. The role of gabapentin in treating diseases with cutaneous manifestations and pain.  Int J Dermatol. 2003;42(6):491-495
PubMed   |  Link to Article
Yesudian PD, Wilson NJ. Efficacy of gabapentin in the management of pruritus of unknown origin.  Arch Dermatol. 2005;141(12):1507-1509
PubMed   |  Link to Article
Winhoven SM, Coulson IH, Bottomley WW. Brachioradial pruritus: response to treatment with gabapentin.  Br J Dermatol. 2004;150(4):786-787
PubMed   |  Link to Article
Kanitakis J. Brachioradial pruritus: report of a new case responding to gabapentin.  Eur J Dermatol. 2006;16(3):311-312
PubMed
Yilmaz S, Ceyhan AM, Baysal Akkaya V. Brachioradial pruritus successfully treated with gabapentin.  J Dermatol. 2010;37(7):662-665
PubMed   |  Link to Article

Figures

Tables

Table Graphic Jump LocationTable. Patients With Scalp Dysesthesia and Cervical Spine Imaging

References

Hoss D, Segal S. Scalp dysesthesia.  Arch Dermatol. 1998;134(3):327-330
PubMed   |  Link to Article
Marziniak M, Phan NQ, Raap U,  et al.  Brachioradial pruritus as a result of cervical spine pathology: the results of a magnetic resonance tomography study.  J Am Acad Dermatol. 2011;65(4):756-762
PubMed   |  Link to Article
Savk E, Savk O, Bolukbasi O,  et al.  Notalgia paresthetica: a study on pathogenesis.  Int J Dermatol. 2000;39(10):754-759
PubMed   |  Link to Article
Raison-Peyron N, Meunier L, Acevedo M, Meynadier J. Notalgia paresthetica: clinical, physiopathological and therapeutic aspects: a study of 12 cases.  J Eur Acad Dermatol Venereol. 1999;12(3):215-221
PubMed   |  Link to Article
Alai NN, Skinner HB, Nabili ST, Jeffes E, Shahrokni S, Saemi AM. Notalgia paresthetica associated with cervical spinal stenosis and cervicothoracic disk disease at C4 through C7.  Cutis. 2010;85(2):77-81
PubMed
Fumal A, Schoenen J. Tension-type headache: current research and clinical management.  Lancet Neurol. 2008;7(1):70-83
PubMed   |  Link to Article
Matsumoto M, Fujimura Y, Suzuki N,  et al.  MRI of cervical intervertebral discs in asymptomatic subjects.  J Bone Joint Surg Br. 1998;80(1):19-24
PubMed   |  Link to Article
Scheinfeld N. The role of gabapentin in treating diseases with cutaneous manifestations and pain.  Int J Dermatol. 2003;42(6):491-495
PubMed   |  Link to Article
Yesudian PD, Wilson NJ. Efficacy of gabapentin in the management of pruritus of unknown origin.  Arch Dermatol. 2005;141(12):1507-1509
PubMed   |  Link to Article
Winhoven SM, Coulson IH, Bottomley WW. Brachioradial pruritus: response to treatment with gabapentin.  Br J Dermatol. 2004;150(4):786-787
PubMed   |  Link to Article
Kanitakis J. Brachioradial pruritus: report of a new case responding to gabapentin.  Eur J Dermatol. 2006;16(3):311-312
PubMed
Yilmaz S, Ceyhan AM, Baysal Akkaya V. Brachioradial pruritus successfully treated with gabapentin.  J Dermatol. 2010;37(7):662-665
PubMed   |  Link to Article

Correspondence

CME
Meets CME requirements for:
Browse CME for all U.S. States
Accreditation Information
The American Medical Association is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. The AMA designates this journal-based CME activity for a maximum of 1 AMA PRA Category 1 CreditTM per course. Physicians should claim only the credit commensurate with the extent of their participation in the activity. Physicians who complete the CME course and score at least 80% correct on the quiz are eligible for AMA PRA Category 1 CreditTM.
Note: You must get at least of the answers correct to pass this quiz.
You have not filled in all the answers to complete this quiz
The following questions were not answered:
Sorry, you have unsuccessfully completed this CME quiz with a score of
The following questions were not answered correctly:
Commitment to Change (optional):
Indicate what change(s) you will implement in your practice, if any, based on this CME course.
Your quiz results:
The filled radio buttons indicate your responses. The preferred responses are highlighted
For CME Course: A Proposed Model for Initial Assessment and Management of Acute Heart Failure Syndromes
Indicate what changes(s) you will implement in your practice, if any, based on this CME course.
NOTE:
Citing articles are presented as examples only. In non-demo SCM6 implementation, integration with CrossRef’s "Cited By" API will populate this tab (http://www.crossref.org/citedby.html).
Submit a Comment

Multimedia

Some tools below are only available to our subscribers or users with an online account.

Related Content

Customize your page view by dragging & repositioning the boxes below.

Related Topics
PubMed Articles
Scalp dysesthesia related to cervical spine disease. JAMA Dermatol 2013;149(2):200-3.