Drabent Philippe, Fraitag Sylvie
Department of Pathology, Necker-Enfants Malades Hospital, APHP, 75015 Paris, France.
Faculté de Médecine, Université de Paris, 75005 Paris, France.
Cancers (Basel). 2022 Apr 26;14(9):2160. doi: 10.3390/cancers14092160.
Malignant superficial mesenchymal tumors are a very diverse group of neoplasms with few clinical and radiological discriminatory factors. Hence, some of these cancers are rarely suspected based on clinical and radiological grounds, others may be easily misdiagnosed, and the histological analysis of a biopsy or resection is central in the diagnostic process. In children, the age at presentation is a major element of the differential diagnosis. Some tumors have a very distinct epidemiology, while others may be seen at any age. More recently, the advances in molecular biology have greatly improved the diagnosis of mesenchymal tumors and new entities are still being described. In the present review, we provide an overview of the diversity of malignant superficial mesenchymal tumors in children, including new and/or rare entities. We discuss the important diagnostic features, be they clinical, histological, or molecular. Special attention was given to the genetic features of these tumors, particularly when they were helpful for the diagnosis or treatment.
恶性浅表间叶组织肿瘤是一组非常多样化的肿瘤,临床和放射学鉴别因素很少。因此,其中一些癌症很少基于临床和放射学依据被怀疑,另一些可能很容易被误诊,活检或切除标本的组织学分析在诊断过程中至关重要。在儿童中,发病年龄是鉴别诊断的主要因素。一些肿瘤具有非常独特的流行病学特征,而另一些则可见于任何年龄。最近,分子生物学的进展极大地改善了间叶组织肿瘤的诊断,并且仍在描述新的实体。在本综述中,我们概述了儿童恶性浅表间叶组织肿瘤的多样性,包括新的和/或罕见的实体。我们讨论重要的诊断特征,无论是临床、组织学还是分子特征。特别关注了这些肿瘤的遗传学特征,尤其是当它们有助于诊断或治疗时。