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Year : 2020  |  Volume : 12  |  Issue : 1  |  Page : 74-75

Syndromes with involvement of multiple cranial nerves: An overview

Department of Medicine, Federal University of Santa Maria, Santa Maria, Rio Grande Do Sul, Brazil

Date of Submission30-Dec-2019
Date of Acceptance31-Dec-2019
Date of Web Publication26-Mar-2020

Correspondence Address:
Jamir Pitton Rissardo
Rua Roraima, Santa Maria, Rio Grande Do Sul
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/ijmbs.ijmbs_87_19

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How to cite this article:
Rissardo JP, Fornari Caprara AL. Syndromes with involvement of multiple cranial nerves: An overview. Ibnosina J Med Biomed Sci 2020;12:74-5

How to cite this URL:
Rissardo JP, Fornari Caprara AL. Syndromes with involvement of multiple cranial nerves: An overview. Ibnosina J Med Biomed Sci [serial online] 2020 [cited 2021 Sep 17];12:74-5. Available from: http://www.ijmbs.org/text.asp?2020/12/1/74/280205

Dear Editor,

We read the article entitled “Retropharyngeal soft-tissue mass with multiple cranial neuropathies” on the esteemed “Ibnosina Journal of Medicine and Biomedical Sciences” with great interest. Bennour et al. reported a case of a middle-aged male who presented with hemifacial pain. Later, the patient developed lesions from the third to the twelfth cranial nerves. A diagnosis of inflammatory pseudotumor of the retropharynx infiltrating the base of the skull and extending to the cavernous sinus was made.[1]

Herein, we would like to provide a table [Table 1] and a figure [Figure 1] to better comprehend the syndromes with the involvement of multiple cranial nerves.[2],[3],[4],[5] Any process that affects the intracranial region may lead to lesions in more than one cranial nerve. In some conditions, a group of nerves can be affected in a specific anatomical region or following some anatomical pattern.[2] Throughout the years, many studies showed patterns of lesions and the discoverers entitled these patterns with their own names; some of these eponyms are present in [Table 1]. These syndromes usually develop gradually and their clinical presentation may be complex, which explains their late diagnosis not being infrequent.[4]
Table 1: Syndromes with involvement of multiple cranial nerves

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{Figure 1}

We included the Avellis', Jackson's, and Schmidt's syndromes to the table and figure. Some authors believe that these syndromes belong to the brainstem syndrome because they can also appear due to the vascular lesions to the medulla. However, it is worthy of mentioning that epidemiological studies showed that they more commonly occur due to extramedullary lesions.[2] With this background, we can assume that the syndrome presented by Bennour et al. is Garcin's.[1] Therefore, we believe that the knowledge of these eponyms can help in the clinical practice to prompt localize the lesion, give a probabilistic etiological diagnosis, and avoid unnecessary examinations.

Author contributions

JPR and ALFC contributed equally. The figure was drawn by JPR.

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Conflicts of interest

There are no conflicts of interest.

Compliance with ethical principles

Not applicable.

  References Top

Bennour AM, Dughman AA, Elkhashmee A. Retropharyngeal soft-tissue mass with multiple cranial neuropathies. Ibnosina J Med Biomed Sci 2019;11:185-7.  Back to cited text no. 1
  [Full text]  
Campbell WW. Brainstem and multiple cranial nerve syndromes. Dejong's the Neurologic Examination. 7th ed. Philadelphia: Lippincott Williams and Wilkins; 2013. p. 335-56.  Back to cited text no. 2
Barker RA, Scolding N, Rowe D, Larner AJ. The AZ of Neurological Practice: A Guide to Clinical Neurology. United Kingdom: Cambridge University Press; 2005. p. 367.  Back to cited text no. 3
Gutiérrez Ríos R, Castrillo Sanz A, Gil Polo C, Zamora García MI, Morollón Sánchez-Mateos N, Mendoza Rodríguez A. Collet-Sicard syndrome. Neurologia 2015;30:130-2.  Back to cited text no. 4
Keane JR. Combined VI and XII cranial nerve palsies: A clival syndrome. Neurology 2000;54:1540-1.  Back to cited text no. 5


  [Figure 7]

  [Table 1]


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