Solitary fibrous tumor of the middle ear: Immunoexpression of NAB2-STAT6 fusion gene
Solitary fibrous tumor of the middle ear: Immunoexpression of NAB2-STAT6 fusion gene
复制标题
中耳孤立性纤维瘤:NAB2-STAT6融合基因的免疫表达
DOI:
10.1016/j.xocr.2021.100345
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发表时间:
2021
影响因子:
--
通讯作者:
Suzuki Masashi
中科院分区:
文献类型:
--
作者:
Tateyama Kaori;Hamada Masashi;Kawano Toshiaki;Kusaba Takahiro;Daa Tsutomu;Suzuki Masashi
ObjectiveTo describe the clinical and pathological findings of a rare case of a solitary fibrous tumor (SFT) arising in the left middle ear, treated with middle ear surgery.PatientA 51-year-old woman presented with a 5-month history of left hearing loss and otalgia. Preoperative otoscopic findings revealed a pulsating blue mass, leading us to the diagnosis of a glomus tympanicum tumor. The tumor was completely resected with mastoidectomy using the facial recess approach. Histopathology showed cells with a low nuclear-to-cytoplasm ratio, having a uniform short spindle-shaped and circular, densely stained nucleus. By immunostaining, the cells werebcl-2andSTAT6-positive. Using a chimeric gene search of the surgically resected specimen, theNAB2-STAT6fusion gene was detected. The patient was finally diagnosed with SFT. No recurrence was found in the 36-month computed tomography follow-up.ConclusionsExtrapleural SFTs have often been reported but no SFT arising in the middle ear have ever been reported in the literature. The SFT of the middle ear had similar clinical manifestations as the glomus tumor in that they are hypervascular neoplastic lesions. Immunoexpression of theNAB2-STAT6fusion gene were useful for the diagonosis of SFT.
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影响因子:
--
作者:
Yoon CM;Cho JM;Lim KR;Kim SK;Kim SJ;Lee KC
通讯作者:
Lee KC
影响因子:
1.7
作者:
Sanna, Mario;Fois, Paolo;Bacciu, Andrea
通讯作者:
Bacciu, Andrea
DOI:
10.1016/j.anl.2016.07.010
发表时间:
2017
期刊:
Auris, nasus, larynx
影响因子:
--
作者:
Munehito Moriyama;S. Kodama;T. Hirano;Masashi Suzuki
通讯作者:
Masashi Suzuki
影响因子:
1.6
作者:
K. Yammine;H. Nasser;U. Hadi;M. Natout;V. Najjar;C. Tayar
通讯作者:
C. Tayar
影响因子:
1.7
作者:
Izumaru, S;Yoshida, Y;Nakashima, T
通讯作者:
Nakashima, T