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Orbital lipofibromatosis in a child: a case report.

机译:儿童眼眶脂肪纤维瘤病:一例报告。

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PURPOSE: Lipofibromatosis is a rare, benign, soft tissue tumor that typically involves extremities particularly in children. We report a young girl with lipofibromatosis involving the superotemporal quadrant of the left orbit. CASE REPORT: An 8-year-old girl presented with a history of a gradually expanding mass in the superotemporal quadrant of the left orbit over several years. Orbital imaging showed a soft tissue mass superolateral to the globe with possible infiltration into the lacrimal gland and lateral rectus muscle. The lesion was excised preserving adjacent structures. Histopathological examination revealed that the lesion consisted of adipose tissue with fibroblastic elements, being consistent with a diagnosis of lipofibromatosis. No recurrence of the lesion was seen in 18 months follow-up. COMMENT: Orbital involvement of lipofibromatosis as reported here is indeed a very rare entity. Diagnosis can be confirmed by histopathological analysis. As the lesion has a tendency to infiltrate into surrounding structures, surgical excision without hampering important structures is a treatment of choice.
机译:目的:脂肪纤维瘤病是一种罕见的良性软组织肿瘤,通常累及四肢,尤其是儿童。我们报告了一个脂纤维瘤病的年轻女孩,累及左眼眶颞上象限。病例报告:一位8岁的女孩,有几年来在左眼眶颞象限中肿块逐渐扩大的历史。眼眶影像学检查显示软组织块位于眼球上方,可能渗入泪腺和直肌外侧。切除病灶,保留邻近结构。组织病理学检查显示,病变由具有纤维母细胞成分的脂肪组织组成,与脂纤维瘤病的诊断一致。在18个月的随访中未见病变复发。评论:此处报道的脂肪纤维瘤病的眼眶侵犯确实是非常罕见的。诊断可通过组织病理学分析确认。由于病变倾向于渗入周围结构,因此在不妨碍重要结构的情况下进行手术切除是一种治疗选择。

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