Saddik M, Oldring D J, Mourad W A
Department of Pathology, University of Alberta Hospitals, Edmonton, Canada.
Arch Pathol Lab Med. 1996 Mar;120(3):292-5.
Liposarcomas of the head and neck are exceedingly rare, and fewer than 90 cases have been reported in the literature. Liposarcoma of the oral cavity is an even less common entity, and to our knowledge only nine cases have been reported to date. We report the clinical and pathologic findings of a case of well-differentiated liposarcoma of the base of tongue and tonsillar fossa. The patient is a 76-year-old white man with a long-standing history of a mass in the oral cavity and hypopharynx. The mass had been resected several times over the span of 23 years, and diagnoses of lipoma, neurofibroma, mesenchymoma, and angiofibrolipoma have been rendered on different occasions. At the last admission, a polypoid mass of the left tonsillar fossa and base of tongue was resected. The tumor was multinodular and measured 2.5 cm in greatest diameter. Histologically the tumor was ill-defined with infiltrating borders and was composed predominantly of mature adipose tissue with occasional lipoblasts. A small proportion of the tumor consisted of clusters of spindle cells and pleomorphic lipoblasts. Mitotic activity was not seen. The pleomorphic cells were positive for S100 protein and negative for muscle-specific markers. Ultrastructural analysis confirmed the nature of the lipoblasts. Our case depicts the typical natural history and histologic features of liposarcoma of the oral cavity. This tumor is usually well differentiated and has a high recurrence rate and almost no tendency for metastasis. Based on our case and review of the literature, it appears that well-differentiated liposarcoma of the oral cavity can occasionally be underdiagnosed because of the low mitotic activity and long latent period between the original diagnosis and first recurrence.
头颈部脂肪肉瘤极为罕见,文献报道不足90例。口腔脂肪肉瘤更是少见,据我们所知,迄今为止仅有9例报道。我们报告1例舌根部和扁桃体窝高分化脂肪肉瘤的临床及病理表现。患者为76岁白人男性,口腔和下咽肿物病史已久。在23年期间该肿物曾多次切除,不同时期诊断为脂肪瘤、神经纤维瘤、间叶瘤和血管纤维脂肪瘤。最后一次入院时,切除了左侧扁桃体窝和舌根部的息肉样肿物。肿瘤呈多结节状,最大直径2.5 cm。组织学上,肿瘤边界不清,呈浸润性生长,主要由成熟脂肪组织构成,偶见脂肪母细胞。肿瘤的一小部分由梭形细胞簇和多形性脂肪母细胞组成。未见核分裂象。多形性细胞S100蛋白阳性,肌肉特异性标志物阴性。超微结构分析证实了脂肪母细胞的性质。我们的病例描述了口腔脂肪肉瘤的典型自然病程和组织学特征。该肿瘤通常分化良好,复发率高,几乎无转移倾向。基于我们的病例并复习文献,似乎口腔高分化脂肪肉瘤偶尔会因核分裂活性低以及初次诊断与首次复发之间的潜伏期长而被漏诊。