Infratemporal Fossa Synovial Sarcoma In A 3-Month-Old Infant: An Extremely Rare Tumour In Infancy.

Q3 Medicine The gulf journal of oncology Pub Date : 2021-09-01 DOI:10.15557/pimr.2021.0057
Nur Adillah Lamry, K. Misron, T. M. I. Tengku Kamalden, S. Mohamad
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Abstract

Soft tissue sarcoma, especially synovial sarcoma is extremely rare in infancy. Only few cases were reported, and challenges lies in disease eradication and subsequent adjuvant therapy. Due to particularly small size of head and neck region with important structures are in intimate location with each other, surgical resection is very challenging, in order to ensure total disease resection as well as maintaining function and cosmetic outcome post-operatively. We present an uncommon case of synovial sarcoma of infratemporal fossa diagnosed in a 3-month-old infant. Due to extreme age, it poses difficulty to the managing team with regards to surgical intervention and oncological regimes. Keywords : Synovial sarcoma; infratemporal fossa; infant.
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3个月婴儿颞下窝滑膜肉瘤:一种极为罕见的婴儿肿瘤。
软组织肉瘤,尤其是滑膜肉瘤在婴儿期极为罕见。只有少数病例报告,挑战在于疾病的根除和随后的辅助治疗。由于头颈部区域体积特别小,重要结构相互靠近,手术切除是非常具有挑战性的,既要保证疾病的完全切除,又要保证术后功能和美观。我们报告一例罕见的颞下窝滑膜肉瘤的诊断在一个3个月大的婴儿。由于极端年龄,它给管理团队在手术干预和肿瘤治疗方面带来了困难。关键词:滑膜肉瘤;颞颥骨下的窝;婴儿。
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来源期刊
The gulf journal of oncology
The gulf journal of oncology Medicine-Medicine (all)
CiteScore
0.90
自引率
0.00%
发文量
37
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