Araştırma Çıktıları

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Subject: search.filters.subject.Schwannoma

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    Ultrasound-Guided Microsurgical Excision for Brachial Plexus Schwannomas: Short-Term Clinical Study
    (TURKISH NEUROSURGICAL SOC, 2019-01-01) Yuce, Ismail; Kahyaoglu, Okan; Mertan, Pelin; Cavusoglu, Halit; Aydin, Yunus
    AIM: To describe the ultrasound-guided microsurgical excision technique and to evaluate the surgical outcomes of brachial plexus schwannomas. MATERIAL and METHODS: Eleven patients who underwent ultrasound-guided microsurgery for small (<3 cm) brachial plexus schwannomas between 2013 and 2017 were included in our study. RESULTS: The mean age of the patients was 45 years (range: 30-68 years), with six tumors localized on the right and five on the left side. There were no perioperative or postoperative complications. No postoperative deficits were observed in the patients. CONCLUSION: Surgeons can safely and completely excise most of the benign (<3 cm and non-palpable) brachial plexus tumors by the ultrasound-guided microsurgical excision technique.
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    Schwannoma of the clitoris: a case report
    (IMR PRESS, 2021-01-01) Kocak, Alper; Selam, Belgin; Akar, Eylem; Erkanli, Serkan
    Schwannoma (neurilemoma or neurinoma) is a tumor that develops from the Schwann cells in the myelin sheath of the peripheral nerves. It is most commonly observed on the head, neck, upper and lower extremities, posterior mediastinum and retroperitoneum. Schwannomas are rarely found in the external female genitalia. To the best of our knowledge, only 6 cases of clitoral schwannoma have been reported in medical literature. We currently report the case of a 46-year-old woman who was presenting with a 3 X 2 cm, painless mass in her clitoris for the past two years. She has no history of neurofibromatosis. Surgical excision of the mass was undertaken. Histopathology and immunohistochemistry revealed schwannoma of the clitoris. No evidence of local recurrence was noted after 6 months of follow-up. We are reporting the current patient because of the rare location of schwannoma. In the present case report, clinical features, treatment guidelines, diagnostic features and the immunohistochemical characteristics of this tumor are reviewed.