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DOI 10.1097/mao.0b013e31814b2285

Медицинская библиотека · Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology · 2007

Cyclin D1 expression and histopathologic features in vestibular schwannomas.

Lassaletta Luis, Patrón Mercedes, Del Río Laura, Alfonso Carolina, Roda Jose Maria, Rey Juan A, Gavilan Javier

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

To evaluate cyclin D1 expression in vestibular schwannoma and its relationship with histologic, clinical, and radiologic features.

PATIENTS: Twenty-one patients with histologically confirmed vestibular schwannoma.

INTERVENTION: Immunohistochemistry analysis was performed with anticyclin D1. Histopathologic features studied included Antoni pattern and nuclear and stromal degenerative changes. Clinical charts, audiometric data, and magnetic resonance imaging characteristics were reviewed.

MAIN OUTCOME MEASURES: Cyclin D1 expression and its association with histologic, clinical, and radiologic findings.

RESULTS

Cyclin D1 expression was found in 52% of cases. Cyclin D1 expression was more frequent in right-sided tumors (p = 0.02) and in tumors with nuclear degenerative changes (p < 0.0001). Patients with negative cyclin D1 expression had longer duration of deafness (p = 0.02) and higher 2,000-Hz hearing thresholds (p = 0.04) than cyclin D1+ patients.

CONCLUSION

Cyclin D1 expression, present in nearly half of the cases, may play a role in the development of these tumors. Further studies are needed to fully understand the contributions of histopathologic and immunohistochemical factors to vestibular schwannoma biological activity.

Для цитирования: Lassaletta Luis, Patrón Mercedes, Del Río Laura, Alfonso Carolina, Roda Jose Maria, Rey Juan A, Gavilan Javier. Cyclin D1 expression and histopathologic features in vestibular schwannomas.. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 2007. DOI: 10.1097/mao.0b013e31814b2285.

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