Mohanna Farah, Slaibi Anas, Al-Shehabi Zuheir, Mahfoud Moufid
Department of Pathology, Cancer Research Center at Tishreen University Hospital, Lattakia, Syria.
J Surg Case Rep. 2020 Jul 14;2020(7):rjaa138. doi: 10.1093/jscr/rjaa138. eCollection 2020 Jul.
Head and neck osteosarcomas are infrequent and usually present in the third-fourth decades of life. However, they are extremely rare in the pediatric population. Primary involvement of the cranial vault, excluding the mandible and maxilla, is an exceedingly rare phenomenon; thus, the number of clinical studies published in the literature is limited. Because of the anatomy of the head, complete resection may be difficult to achieve. Furthermore, an aggressive surgical approach can cause a significant functional impairment or cosmetic defect. We report the case of a 17-year-old patient with an aggressive recurrence of multiple tumors in the left side of the skull accompanied with a severe headache and complete left-sided vision loss with no metastases at presentation. The recurrence of the tumor was preceded by pregnancy and delivery, which raised the question of whether pregnancy hormones were a provoking factor in the recurrence of the tumor or not.
头颈部骨肉瘤较为罕见,通常出现在人生的第三至第四个十年。然而,它们在儿科人群中极为罕见。颅骨穹窿(不包括下颌骨和上颌骨)的原发性受累是一种极其罕见的现象;因此,文献中发表的临床研究数量有限。由于头部的解剖结构,可能难以实现完全切除。此外,积极的手术方法可能会导致严重的功能障碍或美容缺陷。我们报告了一例17岁患者的病例,该患者左侧颅骨出现多个肿瘤的侵袭性复发,伴有严重头痛和左侧完全失明,就诊时无转移。肿瘤复发之前有过怀孕和分娩,这就引发了一个问题,即妊娠激素是否是肿瘤复发的诱发因素。