TYPE II SINGLETON NEUROFIBROMATOSIS WITH CERVICAL SPINAL SCHWANNOMA: A CASE REPORT

Q: How can I download an article?

To download an article from SID, first log in to the site, search for the article title, and click on the 'Download Article' option.

Q: How can I download an ISI article?

To download an ISI article on SID, enter the keyword or article title in the search bar, view the relevant results, click on the desired article, and select the 'Download Article' option.

Q: How can I access the SID database?

To access the SID database, visit SID.ir, create an account, and log in to access scientific resources.

Q: Is downloading articles from SID free?

Some articles on SID are available for free, while others require payment. Details are specified on the article's page.

AZARPAZHOUH M.R.; SHAHAMI S.R.

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: Journal of Sabzevar University of Medical Sciences Year:2007 | Volume:14 | Issue:2 (44) Page(s): 135-140

Download Full-Text

Persian Verion

View:

1,128

Download:

Cites:

Information Journal Paper

Title

TYPE II SINGLETON NEUROFIBROMATOSIS WITH CERVICAL SPINAL SCHWANNOMA: A CASE REPORT

Author(s)

AZARPAZHOUH M.R. | SHAHAMI S.R. | Issue Writer Certificate

Keywords

NEUROFIBROMATOSISQ3

SCHWANNOMAQ4

HEARING LOSSQ3

Abstract

Background and Purpose: Type II NEUROFIBROMATOSIS is a dominant autosomal genetically transferred disease characterized with multiple SCHWANNOMA and classically with bilateral vestibular SCHWANNOMA. SCHWANNOMA is considered as the main symptom and usually originates from cranial nerves (particularly the 8th pair), nerve roots and distal nerves. In this article, one such case is reported.The Patient: A 20-year-old patient with a history of progressive HEARING LOSS from one year earlier was admitted. The history of the patient indicated a spinal SCHWANNOMA surgery one year before the first visit. No familial history was recorded. On the systemic examination, only a few milk brown spots were observed. On the nervous system examination, low facial sensation along the ophthalmic and maxillary branches of the 5th pair, low OS retina reflex and left ear HEARING LOSS were observed. MR imaging indicated hyper-intense damages in T2 phase from the cerebellar-pons angle, highlighting the mass on the right with the radio-opaque agent. Upon left occipital craniotomy, the calcified rather bleeding tumor underwent resection in the cerebellar-pons area. Pathology results confirmed SCHWANNOMA.Conclusion: The singleton type II NEUROFIBROMATOSIS is rare and consideration of the disorder seems to be essential in the diagnosis of multiple simultaneous tumors in the central nervous system.

Cites

No record.

References

No record.

Cite

APA: Copy

AZARPAZHOUH, M.R., & SHAHAMI, S.R.. (2007). TYPE II SINGLETON NEUROFIBROMATOSIS WITH CERVICAL SPINAL SCHWANNOMA: A CASE REPORT. JOURNAL OF SABZEVAR UNIVERSITY OF MEDICAL SCIENCES, 14(2 (44)), 135-140. SID. https://sid.ir/paper/82608/en

Vancouver: Copy

AZARPAZHOUH M.R., SHAHAMI S.R.. TYPE II SINGLETON NEUROFIBROMATOSIS WITH CERVICAL SPINAL SCHWANNOMA: A CASE REPORT. JOURNAL OF SABZEVAR UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2007;14(2 (44)):135-140. Available from: https://sid.ir/paper/82608/en

IEEE: Copy

M.R. AZARPAZHOUH, and S.R. SHAHAMI, “TYPE II SINGLETON NEUROFIBROMATOSIS WITH CERVICAL SPINAL SCHWANNOMA: A CASE REPORT,” JOURNAL OF SABZEVAR UNIVERSITY OF MEDICAL SCIENCES, vol. 14, no. 2 (44), pp. 135–140, 2007, [Online]. Available: https://sid.ir/paper/82608/en

Related Journal Papers