首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Pathology >Deep-seated huge hibernoma of soft tissue: a rare differential diagnosis of atypical lipomatous tumor/well differentiated liposarcoma
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Deep-seated huge hibernoma of soft tissue: a rare differential diagnosis of atypical lipomatous tumor/well differentiated liposarcoma

机译:软组织深层巨大纤维瘤:非典型脂肪瘤/高分化脂肪肉瘤的罕见鉴别诊断

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摘要

Background: Hibernoma is a rare benign fat-forming soft tissue tumor that differentiates similar to brown fat, hence an origin from remnants of fetal brown adipose tissue has been proposed. Mainly young adults are affected, usually without significant clinical symptoms. Material and methods: We report on four patients with hibernomas, who were treated at our hospital during the last 10 years. The clinicopathologic and immunohistochemical features are presented and treatment and follow-up data discussed. Results: Patients were 2 women and 2 men aged 21-67 years (mean: 45 yrs) who presented with a slowly growing, painless mass. The anatomic location was the thigh, upper arm, lateral thoracic wall and paravertebral soft tissue. Two of them were diagnosed preoperatively through a percutaneous core needle biopsy and the other two underwent surgery because of high clinical and radiological suspicion of liposarcoma. The tumor’s size ranged from 7 cm to 15.5 cm (mean: 11 cm). All were deep-seated subfascial intramuscular masses. Histologically, all four tumors were of the typical variant. All patients underwent a R0-surgical resection of the tumor and they were recurrence-free at last follow-up (mean: 47 months; range: 25-87). Conclusion: Hibernoma may present as huge deep intramuscular soft tissue mass in adults, closely mimicking well differentiated liposarcoma and should be considered in the differential diagnosis of fatty soft tissue tumors in any location. Surgical excision is the treatment of choice. The tumor has no malignant or recurrence potential.
机译:背景:子宫肌瘤是一种罕见的良性脂肪形成性软组织肿瘤,其分化类似于棕色脂肪,因此有人提出了胎儿棕色脂肪组织残留的起源。主要是年轻人受到影响,通常没有明显的临床症状。材料和方法:我们报告了最近十年来在我们医院接受治疗的4例冬眠瘤患者。介绍了临床病理和免疫组织化学特征,并讨论了治疗和随访数据。结果:患者为2名女性和2名年龄在21-67岁(平均45岁)的男性,表现为缓慢增长的无痛肿块。解剖位置是大腿,上臂,胸侧壁和椎旁软组织。其中两个是在术前通过经皮穿刺芯活检诊断出来的,另外两个是因为对脂肉瘤的临床和放射学高度怀疑而接受了手术。肿瘤的大小在7厘米到15.5厘米之间(平均:11厘米)。全部为深部筋膜下肌内包块。从组织学上讲,所有四个肿瘤都是典型的变异。所有患者均接受了R0手术切除肿瘤,并且在最后一次随访中均无复发(平均:47个月;范围:25-87)。结论:成人肝纤维瘤可表现为巨大的深部肌内软组织肿块,与高分化脂肪肉瘤极为相似,因此在任何位置的脂肪软组织肿瘤的鉴别诊断中均应考虑。手术切除是治疗的选择。肿瘤没有恶性或复发潜力。

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