A rare Case of Rhabdomyosarcoma presenting as Gradenigo syndrome in a child

Aakriti Chandra, H. Marfatia, Monankita Sharma, Mruganayani Jadhav, Anav Rattan, Sanket Katkar
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Abstract

Objective: To study a rare case of Rhabdomyosarcoma. Methods: Observational descriptive study of a case, a 3-year-old female child, presenting to our OPD. She was thoroughly examined and radiological investigations (HRCT Temporal bone and MRI Brain) were done. The Neurosurgery department proceeded with a biopsy of the lesion by left temporal bone craniotomy through subtemporal approach. Results: Histopathology suggested a Rhabdomyosarcoma of anaplastic type. The patient then underwent 6 cycles of Chemoradiation. Conclusion: The awareness that Rhabdomyosarcoma of petrous apex can present as Gradenigo syndrome along with 7th nerve palsy is important for the early diagnosis and its treatment.
一例罕见的横纹肌肉瘤的表现为格雷迪尼戈综合征的儿童
目的:研究一例罕见的横纹肌肉瘤。方法:观察性描述性研究的情况下,一个3岁的女童,提出了我们的门诊医生。对患者进行了全面检查和影像学检查(HRCT颞骨和MRI脑)。神经外科通过颞下入路左颞骨开颅对病变进行活检。结果:组织病理学提示为间变性横纹肌肉瘤。患者随后接受了6个周期的放化疗。结论:认识岩尖横纹肌肉瘤伴第七神经麻痹可表现为渐行性麻痹综合征,对其早期诊断和治疗具有重要意义。
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