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眼眶原发性去分化脂肪肉瘤,一种罕见的疾病:病例报告及文献复习

Primary dedifferentiated liposarcoma of the orbit, a rare entity: Case report and review of literature.

作者信息

Andrea Torroni, Giulio Gasparini, Giuliana Longo, Sandro Pelo

机构信息

Department of Plastic Surgery, Division of Oral and Maxillofacial Surgery, New York University, USA.

Department of Maxillofacial Surgery, Catholic University of the Sacred Hearth of Rome, Italy.

出版信息

Saudi J Ophthalmol. 2019 Jul-Sep;33(3):312-315. doi: 10.1016/j.sjopt.2019.01.003. Epub 2019 Jan 16.

Abstract

Head and neck liposarcomas are rare entities accounting for less than 5% of all liposarcomas. The primary orbital location is even rarer, with about 40 cases described in the English literature. According with the widely accepted classification of Enzinger and Weis there are 5 histologic variants of liposarcomas: well differentiated, myxoid, dedifferentiated, round cell and pleomorphic. The first two are considered low-grade and display a favourable prognosis (>90% 5-year DSS and OS), whereas the dedifferentiated, round cell, and pleomorphic are defined high-grade and burdened with poorer prognosis (5-year DSS ranging 45-73%). Dedifferentiated liposarcomas (DDL) of the head and neck region are exceedingly rare, therefore there are scattered and contrasting data regarding their clinical history, treatment modality, and prognosis. We presented a case of DDL arising in the the left orbit (fourth case of primary orbital DDL described), free from disease after 5-year follow-up. Clinical history, treatment, and characteristics of the presented case were described and discussed in the light of how reported in the literature, in the attempt to bring further insight in the nature and management of this rare pathological entity.

摘要

头颈部脂肪肉瘤是罕见的实体瘤,占所有脂肪肉瘤的比例不到5%。其主要发生于眼眶的情况更为罕见,英文文献中仅有约40例相关报道。根据恩津格(Enzinger)和魏斯(Weis)广泛认可的分类,脂肪肉瘤有5种组织学变体:高分化型、黏液型、去分化型、圆形细胞型和多形性型。前两种被认为是低级别,预后良好(5年疾病特异性生存率和总生存率>90%),而去分化型、圆形细胞型和多形性型则被定义为高级别,预后较差(5年疾病特异性生存率为45%-73%)。头颈部区域的去分化脂肪肉瘤(DDL)极其罕见,因此关于其临床病史、治疗方式和预后的数据零散且存在差异。我们报告了一例发生于左眼眶的DDL(文献报道的第四例原发性眼眶DDL),经过5年随访无疾病复发。结合文献报道,对该病例的临床病史、治疗及特征进行了描述和讨论,旨在进一步深入了解这种罕见病理实体的本质和治疗方法。

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