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Brachioradial Pruritus

Editor: George J. Schmieder Updated: 9/12/2022 9:11:54 PM

Introduction

Brachioradial pruritus (BRP) is a localized neuropathic dysesthesia of the dorsolateral upper extremities (see Image. Brachoradialis Pruritus). This condition is commonly seen in middle-aged White women, with a seasonal predilection for warmer summer months. Cervical radiculopathy or neuropathy in the upper extremities, in conjunction with ultraviolet radiation (UVR), is thought to be causative.[1][2][3] Despite the wide variety of etiologies for pruritus, identification of brachioradial pruritus by dermatologists through the history and physical exam has been straightforward. Further workups, such as imaging, labs, and referral to specialists, are rarely required. Therapeutic options are numerous and well-tolerated. Because of the benign transient nature of brachioradial pruritus, the number of reported cases and current studies are relatively low.

Etiology

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Etiology

While not completely elucidated, current theories suggest brachioradial pruritus is a bifactorial process involving cervical nerve irritation and ultraviolet radiation (UVR) of the affected area.[4][5][6]  Most patients diagnosed with brachioradial pruritus have a positive imaging study with evidence of 1 or more cervical spine abnormalities. Imaging with x-ray, computed tomography (CT), or magnetic resonance imaging (MRI) of patients with suspected or diagnosed brachioradial pruritus revealed cervical spine abnormalities such as degenerative joint disease (DJD), cervical nerve impingement due to disk herniation, osteoarthritis, foraminal stenosis, and others. DJD has been reported as the most common cervical spine abnormality in patients with brachioradial pruritus.

Many authors suggest that cervical spine disease between C5 to C8 is causative. The dermatomes of the dorsolateral arms are C5 to C6, and a cervical spine abnormality with evidence of radiculopathy at these levels would be especially suggestive as a cause for brachioradial pruritus. Despite the high frequency of cervical spine abnormalities on imaging, nearly all patients with brachioradial pruritus imaged did not meet the criteria for cervical radiculopathy. Additionally, only a minority of patients diagnosed with brachioradial pruritus are imaged. This suggests that cervical radiculopathy not inclusive of radiologic criteria may be responsible for the high frequency of cervical spinal abnormalities in patients with brachioradial pruritus may simply be a confounding finding.

UVR is thought to be a contributing factor to brachioradial pruritus, and many patients report increased symptoms of brachioradial pruritus with sun exposure. The term brachioradial summer pruritus is also used in reference to the increased incidence of brachioradial pruritus during the warm summer months. A subset of histamine-sensitive C-fibers is responsible for the transmission of pruritus. Excessive UVR causes damage and a reduction of these C-fibers. Despite the reduction in cutaneous C-fiber number, increased pruritus is reported with UVR in patients with brachioradial pruritus. This pruritic response to a stimulus that does not normally cause pruritus is known as alloknesis. Many patients report relief of symptoms during the winter months and with sun protection, which supports the role of UVR as a trigger in brachioradial pruritus. The absence of either radiographically evident cervical nerve irritation or UVR does not preclude the diagnosis of brachioradial pruritus.

Epidemiology

Early isolated case reports suggested that brachioradial pruritus was more common in men. Results from later larger studies revealed that brachioradial pruritus is seen more commonly in women than men in a ratio of 3:1. The mean age at diagnosis is 59, but wide variations in age have been reported. Brachioradial pruritus is more common in lighter skin types, especially those with Fitzpatrick type I and type II skin, than in darker skin types. This factor further supports the role of UVR in the pathogenesis of brachioradial pruritus.

Histopathology

Brachioradial pruritus lacks characteristic histopathological features. Microscopic findings include actinic elastosis and decreased density of epidermal and dermal nerve fibers. Actinic elastosis correlates with a history of extensive UVR exposure. A decrease in the density of nerve fibers is seen with phototherapy treatments and would be consistent with UVR-induced brachioradial pruritus exacerbations during the sunny summer months.

History and Physical

Because pruritus has many etiologies, a thorough history is essential to avoid unnecessary testing and treatment delays. Brachioradial pruritus has a wide presentation area but is most commonly reported on the dorsolateral arms. Adjacent areas that may be affected are in the C5 to C6 dermatome and include the upper arms, shoulders, and neck. In addition to pruritus, patients may report pain, stinging, or tingling in the affected area.

Brachioradial pruritus is bilateral approximately 75% of the time.[7][8][9] Symptoms are usually present for 2 to 3 years before diagnosis. Patients are typically outdoor enthusiasts such as bikers, hikers, and tanners and may have an extensive history of sunburn. Despite the high frequency of cervical spine abnormalities seen on imaging in patients with brachioradial pruritus, retrospective studies report that very few patients had complaints of neck pain, cervical spine narrowing, or neck trauma.

The physical exam of the affected areas is not impressive and lacks primary cutaneous lesions. Secondary cutaneous lesions such as excoriations, prurigo nodules, or lichenification may be present due to excessive scratching. Confounding factors include coexistent chronic pruritic conditions, skin diseases, topical or systemic medications, and unusual presentations.

Evaluation

The ice-pack sign is considered pathognomonic for brachioradial pruritus. The test is simple and involves placing an ice pack on the affected area; the patient should report immediate improvement of pruritus that returns shortly after removing the ice pack. Evaluations beyond a thorough history and physical and the ice-pack test are typically unnecessary. Imaging, blood tests, and referrals to appropriate specialists may be required in recalcitrant cases. Imaging modalities such as x-rays, CTs, and MRIs usually are not required. If imaging of the cervical spine is desired, MRI is the preferred modality. Screening blood work for causes of chronic pruritus can be performed. Referral to neurology for further examinations may be appropriate if a neurological cause is suspected. Neurological examinations include cervical spine imaging and electromyography.

Treatment / Management

Treatment includes avoidance of UVR, topical medications, systemic medications, and, in select cases, surgery. Methods of UVR avoidance include reducing sun exposure, judicious use of sunscreen, and use of long-sleeved UV-protective clothing. This may be difficult for some patients with brachioradial pruritus, as many enjoy outdoor activities during the warm summer. Topical medications include capsaicin, mild steroids, anesthetics, antihistamines, and amitriptyline/ketamine. Earlier reports stated topical capsaicin was the most commonly prescribed initial therapy. A newer study reported the oral tricyclic antidepressant amitriptyline was the most commonly prescribed medication for brachioradial pruritus, although gabapentin may be more efficacious.

Other oral medications include risperidone, fluoxetine, chlorpromazine, and hydroxyzine. For unknown reasons, systemic antihistamine therapies are ineffective in brachioradial pruritus. Response to treatment was greatest in patients who rated their pruritus as severe and those who continued with longer treatments.[10][11][12] The sample size of most studies is small, and differences in the most prescribed and efficacious therapy vary. Surgery was reserved for patients with a correctable cervical spinal abnormality seen on imaging; very few patients fall into this category.(B3)

Differential Diagnosis

The differential diagnoses for brachioradial pruritus include the following:

  • Neurotic excoriations
  • Notalgia paresthetica
  • Zoster sine herpete
  • Atopic dermatitis

Enhancing Healthcare Team Outcomes

The diagnosis and management of BRP are very difficult, and thus, it is managed by an interprofessional team. Communication between the healthcare team improves the coordination of care. Specialty-trained clinicians in dermatology, pain management, and psychiatry may be involved. The condition is more common in middle-aged White women with a seasonal predilection for warmer summer months. Cervical radiculopathy or neuropathy in the upper extremities, in conjunction with ultraviolet radiation, is thought to be causative.

There are hundreds of treatments for the disorder, but none works reliably or is better than other treatments. Patients go through exhaustive workups to determine the cause, which is never found in most cases. Many patients develop severe anxiety and depression and become isolated. In these cases, a mental health clinician and specialty-trained clinicians should be included in the team. The clinicians should educate the patient in the management of pain and pruritus. In addition, the patient should be told to avoid exposure to the sun, wear long-sleeved garments, and keep the skin moisturized. Finally, referral to a pain specialist may be in order if the pain is constant and can vary from moderate to severe. The condition is benign, but it can seriously affect the quality of life because of the constant itching.[3][13]

Media


(Click Image to Enlarge)
<p>Brachoradialis Pruritus

Brachoradialis Pruritus. Brachioradial pruritus is a localized neuropathic dysesthesia of the dorsolateral upper extremities.

Contributed by O Chaigasame, MD

References


[1]

Weinberg BD, Amans M, Deviren S, Berger T, Shah V. Brachioradial pruritus treated with computed tomography-guided cervical nerve root block: A case series. JAAD case reports. 2018 Aug:4(7):640-644. doi: 10.1016/j.jdcr.2018.03.025. Epub 2018 Jul 25     [PubMed PMID: 30094306]

Level 2 (mid-level) evidence

[2]

He A, Alhariri JM, Sweren RJ, Kwatra MM, Kwatra SG. Aprepitant for the Treatment of Chronic Refractory Pruritus. BioMed research international. 2017:2017():4790810. doi: 10.1155/2017/4790810. Epub 2017 Sep 19     [PubMed PMID: 29057261]


[3]

Pereira MP, Lüling H, Dieckhöfer A, Steinke S, Zeidler C, Ständer S. Brachioradial Pruritus and Notalgia Paraesthetica: A Comparative Observational Study of Clinical Presentation and Morphological Pathologies. Acta dermato-venereologica. 2018 Jan 12:98(1):82-88. doi: 10.2340/00015555-2789. Epub     [PubMed PMID: 28902951]

Level 2 (mid-level) evidence

[4]

Alai NN, Skinner HB. Concurrent notalgia paresthetica and brachioradial pruritus associated with cervical degenerative disc disease. Cutis. 2018 Sep:102(3):185;186;189;190     [PubMed PMID: 30372709]


[5]

Vestita M, Cerbone L, Calista D. Brachioradial pruritus in a 47-year-old woman treated with pregabalin. Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia. 2016 Dec:151(6):727-728     [PubMed PMID: 27824228]


[6]

Pinto AC, Wachholz PA, Masuda PY, Martelli AC. Clinical, epidemiological and therapeutic profile of patients with brachioradial pruritus in a reference service in dermatology. Anais brasileiros de dermatologia. 2016 Jul-Aug:91(4):549-51. doi: 10.1590/abd1806-4841.201644767. Epub     [PubMed PMID: 27579762]

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[7]

Atış G, Bilir Kaya B. Pregabalin treatment of three cases with brachioradial pruritus. Dermatologic therapy. 2017 Mar:30(2):. doi: 10.1111/dth.12459. Epub 2017 Feb 6     [PubMed PMID: 28168835]

Level 3 (low-level) evidence

[8]

Strowd RE, Strowd LC, Blakeley JO. Cutaneous manifestations in neuro-oncology: clinically relevant tumor and treatment associated dermatologic findings. Seminars in oncology. 2016 Jun:43(3):401-7. doi: 10.1053/j.seminoncol.2016.02.029. Epub 2016 Feb 23     [PubMed PMID: 27178695]


[9]

Salako KB, Anstey AA, Logan RA. Delayed, transient, postsolar truncal pruritus: a report of two cases. Clinical and experimental dermatology. 2014 Aug:39(6):726-7. doi: 10.1111/ced.12375. Epub 2014 Jul 1     [PubMed PMID: 24986101]

Level 3 (low-level) evidence

[10]

Pereira MP, Lüling H, Dieckhöfer A, Steinke S, Zeidler C, Agelopoulos K, Ständer S. Application of an 8% capsaicin patch normalizes epidermal TRPV1 expression but not the decreased intraepidermal nerve fibre density in patients with brachioradial pruritus. Journal of the European Academy of Dermatology and Venereology : JEADV. 2018 Sep:32(9):1535-1541. doi: 10.1111/jdv.14857. Epub 2018 Mar 9     [PubMed PMID: 29427475]


[11]

Wachholz PA, Masuda PY, Pinto ACVD, Martelli ACC. Impact of drug therapy on brachioradial pruritus. Anais brasileiros de dermatologia. 2017 Mar-Apr:92(2):281-282. doi: 10.1590/abd1806-4841.20175321. Epub     [PubMed PMID: 28538902]


[12]

Zeidler C, Lüling H, Dieckhöfer A, Osada N, Schedel F, Steinke S, Augustin M, Ständer S. Capsaicin 8% cutaneous patch: a promising treatment for brachioradial pruritus? The British journal of dermatology. 2015 Jun:172(6):1669-1671. doi: 10.1111/bjd.13501. Epub 2015 Apr 13     [PubMed PMID: 25354282]

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[13]

Dhand A, Aminoff MJ. The neurology of itch. Brain : a journal of neurology. 2014 Feb:137(Pt 2):313-22. doi: 10.1093/brain/awt158. Epub 2013 Jun 22     [PubMed PMID: 23794605]

Level 3 (low-level) evidence