Adrenal bezden köken alan soliter kistik shwannom
oldukça nadirdir. Retroperitoneal kitlelerin %1-5'ini oluşturmaktadır. Klinik
bulguları non-spesifiktir. Bizim olgumuzda olduğu gibi tesadüfen saptanırlar ve
genel olarak ilk bulguları ağrıdır. Kesin tanı patolojik incelemeyle konur.
Rezeksiyondan sonra prognoz
mükemmeldir. Adrenal bezden köken alan primer adrenal schwannom dünyada nadir
olarak saptanması ve ülkemizde ilk vaka olması nedeniyle yayınlanmaya değer
görülmüştür.
Solitary-cystic Schwannoma arising from adrenal gland
is seen extremely rare. Its frequency in
our country is unknown. Schwannomas are responsible for 1-5% of all
retroperitoneal masses and clinical signs are non-specific. They are diagnosed
incidentally as in our case and generally their first sign is referred pain. CT
and MR are important screening methods. However, the final diagnosis is made by
pathological examination. The prognosis is excellent after total resection. It
is valuable to present the primary adrenal schwannoma arising from adrenal
gland because of its rare incidence in all of the world thus this is the first case in our country.
Primary Language | English |
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Journal Section | Case Report |
Publication Date | December 30, 2016 |
Submission Date | December 28, 2015 |
Acceptance Date | February 1, 2017 |
Published in Issue | Year 2016 Volume: 7 Issue: 28 |