Literature DB >> 23054921

Transient idiopathic isolated unilateral hypoglossal nerve palsy.

Kiyoshi Shikino1, Kazutaka Noda, Masatomi Ikusaka.   

Abstract

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Year:  2012        PMID: 23054921      PMCID: PMC3599034          DOI: 10.1007/s11606-012-2228-9

Source DB:  PubMed          Journal:  J Gen Intern Med        ISSN: 0884-8734            Impact factor:   5.128


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A 33-year-old woman presented with five days of dysarthria and dysphagia. Her past medical history included Graves’ disease treated with a partial thyroidectomy five years earlier. On examination, she had tongue mounding and deviation to the right (Figs. 1 and 2). Other neurological and otorhinolaryngological findings were normal. Titers of herpes simplex virus and varicella-zoster virus antibodies were positive, but did not differ between the acute and convalescent phase sera. Brain magnetic resonance imaging (MRI) and magnetic resonance angiogram (MRA) findings were normal, and laboratory tests showed no evidence of inflammation. Idiopathic isolated unilateral hypoglossal nerve palsy was diagnosed.
Figure 1.

Right tongue mounding at rest.

Figure 2.

Tongue deviation to the right.

Right tongue mounding at rest. Tongue deviation to the right. While cranial nerves III, IV, VI and VII are more prone to idiopathic palsy, idiopathic unilateral hypoglossal nerve palsy is rare. With the limited number of cases reported, the male-to-female ratio appears even, the age of onset is widely distributed (20–69 years) and the majority of cases self-resolve.1 In acute isolated hypoglossal nerve palsy, malignancy, vascular pathology, herpes infection, systemic lupus erythematosus, multiple sclerosis and diabetic mononeuropathy have been reported as causes.1–3 Although the paired sera failed to show acute herpes infection in this case, reactivation of the disease could still be possible. Eight weeks after symptom onset, this patient fully recovered without intervention.
  2 in total

1.  Isolated unilateral hypoglossal nerve palsy: nine cases.

Authors:  O Combarros; A Alvarez de Arcaya; J Berciano
Journal:  J Neurol       Date:  1998-02       Impact factor: 4.849

2.  An unusual case of systemic lupus erythematosus with isolated hypoglossal nerve palsy, fulminant acute pneumonitis, and pulmonary amyloidosis.

Authors:  C N Chan; E Li; F M Lai; J A Pang
Journal:  Ann Rheum Dis       Date:  1989-03       Impact factor: 19.103

  2 in total

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