- Case report
- Open Access
- Open Peer Review
Episodic itch in a case of spinal glioma
© Wolking et al.; licensee BioMed Central Ltd. 2013
- Received: 2 April 2013
- Accepted: 18 September 2013
- Published: 23 September 2013
Itch is a frequent complaint reported by patients and is usually ascribed to dermatological or metabolic causes. In neurological disorders, however, it is a very unusual symptom and thus its neurological aetiology is likely to be overlooked. There are only very few reports about permanent itch related to lesions of the central nervous system. To our knowledge we report the first case of episodic itch associated with a central nervous lesion.
A 74-year-old female suffered from long-standing episodes of itch of the dermatomes C2 to C6 on the right side that was refractory to any treatment. On occurrence it propagated in a proximal to distal fashion. Between the episodes the patient was asymptomatic. MRI of the cervical spine uncovered a spinal glioma that matched the location of the symptoms. Treatment with gabapentin led to a prompt reduction of the symptoms.
Patients with intractable pruritus and dermatomal presentation ought to undergo neurological examination and spinal cord imaging. Thus, ongoing frustrating and sometimes even harmful treatment trials could be avoided.
Chronic itch is a common symptom and often proves to be a diagnostic and therapeutic challenge. It is often related to dermatologic aetiologies. In the absence of skin alteration, metabolic or endocrinologic diseases are frequently diagnosed.
In neurological disorders, however, itch is a rather unusual symptom within which peripheral neural affections such as postherpetic itch after shingles  or radiculopathy due to osteoarthritis  account for the major part. In contrast, central itch is even far less frequent and, predominantly caused by cerebral lesions. It is often caused by cerebral lesions such as brain stem infarction , multiple sclerosis , brainstem glioma  or supratentorial cerebral abscess .
Only few cases are reported on pruritus associated with spine tumours, such as intramedullary astrocytoma in children  and intramedullary cervical ependymoma in adults . Other spinal lesions may be associated with pruritus as well, such as cervical cavernoma , cavernous hemangioma  and vascular malformation .
In all the reported cases, permanent and not episodic itching – as observed in our patient – has been reported. It is also unusual that no other sensory symptoms occurred between the episodes.
A 74-year-old female was admitted to our department with intractable pruritus of the right arm, ear lobe and the right occiput. For 5 to 6 years the pruritus had appeared episodically about every two days lasting for several hours. It usually emerged from the right shoulder and then propagated along the radial side of the arm down to the wrist within few minutes and persist for several hours. Occasionally, the itch emanated from further above, originating from the right side of the back of the head including the right ear lobe with propagation down to the right arm as described before. Apart from scratch marks no rash or skin alterations had been observed in the affected region. Between the episodes, the patient was asymptomatic.
The patient had a history of multiple dermatologic treatment approaches. Amongst others, allergic contact dermatitis and food intolerance syndrome as well as mastocytosis had been suspected, but could not be confirmed. Treatment with topic and oral steroids had shown no positive effect. She reported that intake of the histamine antagonist desloratadine at the onset of symptoms would lead to a relief after two to three hours. Nonetheless, without drug intake, the symptoms would be self-limiting as well. Thus, there was no evidence of any benefit deriving from antihistaminic treatment.
Examination revealed slightly elevated tendon reflexes and Hoffmann’s reflex of the right upper limb and a minor clumsiness of the right hand. Sensibility was intact. In the arm extension test, a heaviness of the right arm was reported, however there was no objectifiable motor deficit. Lower Limb examination showed no reflex abnormalities, no motor deficit and negative pyramid signs. Skin examination revealed no abnormalities.
Somatosensory evoked potentials (SSEP) of the right median nerve showed an increased latency for C7 and C2 whereas cortical recordings were normal. Tibial nerve SSEP showed a symmetrical increase of latency on cortical recordings. Motor evoked potentials (MEP) revealed a borderline decrease of amplitude to the right arm. In order to rule out an inflammatory etiology CSF analysis was perfornerd. It showed no signs of inflammation, atypical cells or prior bleeding.
The patient refused any surgical treatment or biopsy. The long persistence of the symptoms suggested a low growth-rate of the tumour. A control MRI was performed after four months without any change of the tumour mass.
We started the patient on gabapentin (1200 mg/d) which provoked initially a rapid reduction of the pruritus. After 3 months, however, episodic pruritus recurred and gabapentin was discontinued due to fatigue. Afterwards, pregabalin was introduced but withdrawn shortly due to side effects. Oxcarbazepine is now intended as the next drug.
We report a case of longstanding episodic pruritus in association with a cervical intramedullary glioma. To our knowledge it is the first case to report of episodic – not permanent – itch due to a lesion of the central nervous system.
The propagation of the itch within a few minutes in a proximal-distal direction is reminiscent of focal seizures (somato-sensory auras) with spreading paraesthesias, as a sensory Jacksonian march.
Since the cervical lesion between the vertebrae C2 to C5 coincides with the clinical presentation of sensory symptoms restricted to dermatomes C2 to C6, although C6 dermatome was not completely affected leaving out the right thumb, we hypothesize that electrical phenomena similar to epileptic seizures or spreading depression in the cortex might cause the episodic symptoms. The excellent initial response to gabapentin supports this hypothesis. However, gabapentin is used to treat peripheral neuropathy as well and thus its efficacy in this particular case does not prove a central origin of the itch.
Alternatively, variations of the local intraspinal pressure might cause the observed fluctuation.
The existence of spinal cord seizures in humans has been postulated by several authors in association with multiple sclerosis , spinal ischemia  and traumatic injury . In most cases the seizures were focal-motor or myoclonic and were often associated with dysaesthesia in the affected limb . In several cases a response to antiepileptic drugs such as carbamazepine and benzodiazepines was reported [12, 14].
Chronic itch is a very trying and cumbersome burden for the affected patients and a diagnostic and therapeutic challenge for the practitioners. If dermatological and metabolic tests yield no explanation diagnostics should be extended. Especially, patients with episodic occurrence of itch, a dermatomal localization and progression should be referred to neurological examination and eventually spinal cord imaging. These patients may profit from antiepileptic treatment.
Written informed consent was obtained from the patient for publication of this Case report and the accompanying images. A copy of the written consent is available for review by the Editor of this journal.
- Oaklander AL: Common neuropathic itch syndromes. Acta Derm Venereol. 2012, 92 (2): 118-125. 10.2340/00015555-1318.View ArticlePubMedGoogle Scholar
- Eisenberg E, Barmeir E, Bergman R: Notalgia paresthetica associated with nerve root impingement. J Am Acad Dermatol. 1997, 37 (6): 998-1000. 10.1016/S0190-9622(97)70083-5.View ArticlePubMedGoogle Scholar
- Fitzek S, Baumgartner U, Marx J, Joachimski F, Axer H, Witte OW, et al: Pain and itch in Wallenberg’s syndrome: anatomical-functional correlations. Suppl Clin Neurophysiol. 2006, 58: 187-194.View ArticlePubMedGoogle Scholar
- Yamamoto M, Yabuki S, Hayabara T, Otsuki S: Paroxysmal itching in multiple sclerosis: a report of three cases. J Neurol Neurosurg Psychiatry. 1981, 44 (1): 19-22. 10.1136/jnnp.44.1.19.View ArticlePubMedPubMed CentralGoogle Scholar
- Summers CG, MacDonald JT: Paroxysmal facial itch: a presenting sign of childhood brainstem glioma. J Child Neurol. 1988, 3 (3): 189-192. 10.1177/088307388800300308.View ArticlePubMedGoogle Scholar
- Sullivan MJ, Drake ME: Unilateral pruritus and Nocardia brain abscess. Neurology. 1984, 34 (6): 828-829. 10.1212/WNL.34.6.828.View ArticlePubMedGoogle Scholar
- Magilner D: Localized cervical pruritus as the presenting symptom of a spinal cord tumor. Pediatr Emerg Care. 2006, 22 (10): 746-747. 10.1097/01.pec.0000238735.14532.2e.View ArticlePubMedGoogle Scholar
- Fleuret C, Dupre-Goetghebeur D, Person H, Pillette-Delarue M, Conan-Charlet V, Meriot P, et al: Brachioradial pruritus revealing an ependymoma. Ann Dermatol Venereol. 2009, 136 (5): 435-437. 10.1016/j.annder.2008.11.020.View ArticlePubMedGoogle Scholar
- Dey DD, Landrum O, Oaklander AL: Central neuropathic itch from spinal-cord cavernous hemangioma: a human case, a possible animal model, and hypotheses about pathogenesis. Pain. 2005, 113 (1–2): 233-237.View ArticlePubMedGoogle Scholar
- Lanotte M, Panciani PP, Magistrello M, Naldi A, Fontanella M, Ducati A, Giordana MT: Central neuropathic itch as the presenting symptom of an intramedullary cavernous hemangioma: case report and review of literature. Clin Neurol Neurosurg. 2013, 115 (4): 454-456. 10.1016/j.clineuro.2012.05.028.View ArticlePubMedGoogle Scholar
- Vuadens P, Regli F, Dolivo M, Uske A: Segmental pruritus and intramedullary vascular malformation. Schweiz Arch Neurol Psychiatr. 1994, 145 (3): 13-16.PubMedGoogle Scholar
- Cherrick AA, Ellenberg M: Spinal cord seizures in transverse myelopathy: report of two cases. Arch Phys Med Rehabil. 1986, 67 (2): 129-131. 10.1016/0003-9993(86)90125-5.View ArticlePubMedGoogle Scholar
- Ekbom KA, Westerberg CE, Osterman PO: Focal sensory-motor seizures of spinal origin. Lancet. 1968, 1 (7533): 67-View ArticlePubMedGoogle Scholar
- Meythaler JM, Tuel SM, Cross LL: Spinal cord seizures: a possible cause of isolated myoclonic activity in traumatic spinal cord injury: case report. Paraplegia. 1991, 29 (8): 557-560. 10.1038/sc.1991.81.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2377/13/124/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.