Parosteal lipoma of the supra-auricular region.

Surgical neurology international Pub Date : 2025-06-20 eCollection Date: 2025-01-01 DOI:10.25259/SNI_289_2025
Made Ratna Dewi, Christopher Lauren, I Nyoman Gde Wahyudana, Analysa Analysa, Ida Bagus Gede Adiguna Wibawa, I Gusti Ketut Agung Surya Kencana, Tjokorda Gde Bagus Mahadewa
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Abstract

Background: Parosteal lipomas are rare benign soft-tissue tumors that develop in close association with the periosteum. Skull involvement is exceptionally uncommon, with only a few cases reported in the literature.

Case description: A 14-year-old female presented with a slowly enlarging, painless lump above her right ear, first noticed at the age of five. Physical examination revealed a firm, well-defined, immobile mass measuring 2.5 × 1.5 cm in the supra-auricular region. A non-contrast computed tomography scan demonstrated a hypodense mass with thickening of the underlying squamous and mastoid bones, along with mastoid air cell enlargement. Surgical excision was performed for cosmetic reasons and histopathological diagnosis. Intraoperatively, the mass was found to be adherent to the periosteum and underlying bone. Histopathological examination confirmed the diagnosis of parosteal lipoma, showing mature adipose tissue, fibrous tissue, and focal lymphocytic aggregates without signs of malignancy. The patient recovered well postoperatively, with no recurrence or complications over 6 months of follow-up.

Conclusion: Parosteal lipomas of the skull are exceedingly rare and require clinical suspicion for diagnosis. Imaging aids in preoperative planning, while histopathological assessment confirms the diagnosis. Complete surgical excision is curative, with a favorable prognosis. This case adds to the limited literature on skull-based parosteal lipomas.

耳上区域的腺旁脂肪瘤。
背景:腮腺脂肪瘤是一种罕见的良性软组织肿瘤,其发展与骨膜密切相关。颅骨受累是非常罕见的,文献中只有少数病例报道。病例描述:一名14岁女性,5岁时首次发现右耳上方有一个缓慢增大的无痛性肿块。体格检查发现在耳上区有一个坚固、界限分明、固定的肿块,大小为2.5 × 1.5 cm。非对比计算机断层扫描显示低密度肿块,其下鳞状骨和乳突骨增厚,同时乳突空气细胞增大。手术切除的原因是美容和组织病理学诊断。术中发现肿块附着于骨膜和下骨。组织病理学检查证实了腮腺脂肪瘤的诊断,显示成熟的脂肪组织、纤维组织和局灶性淋巴细胞聚集,没有恶性肿瘤的迹象。患者术后恢复良好,随访6个月无复发及并发症发生。结论:颅骨旁腺脂肪瘤极为罕见,需要临床怀疑诊断。影像学有助于术前计划,而组织病理学评估证实了诊断。完全手术切除可治愈,预后良好。本病例增加了关于颅骨为基础的腮腺脂肪瘤的有限文献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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