{"title":"Classification and a practical pattern-based approach to the diagnosis of adipocytic tumors","authors":"David Creytens","doi":"10.1016/j.mpdhp.2026.07.005","DOIUrl":null,"url":null,"abstract":"<div><div>Adipocytic tumors are among the most common mesenchymal neoplasms in general surgical pathology. These tumors encompass a broad histological spectrum with variable degrees of adipocytic differentiation and a wide range of clinical behaviour, varying from entirely benign lipomas to aggressive pleomorphic liposarcomas. The World Health Organization (WHO) classification of adipocytic tumors has evolved considerably in the last decades, largely due to important advances in understanding their pathogenetic basis. Although classic examples of lipomas and liposarcomas are straightforward diagnoses, primarily distinguished by their morphological characteristics, several lipomatous tumors are now known to show unique, recurrent molecular genetic aberrations, identification of which can be used in the diagnostic work-up of distinct (uncommon) lipomatous tumor variants and histologically ambiguous adipocytic tumors. This article will provide a practical pattern-based approach to the histological diagnosis of benign, intermediate and malignant adipocytic neoplasms. We will focus on the currently known morphological, immunohistochemical and molecular features of the different adipocytic tumor entities, discuss their differential diagnoses and update on recently described adipocytic tumor entities (lipoblastoma-like tumor, atypical spindle cell/pleomorphic lipomatous tumor, and myxoid pleomorphic liposarcoma).</div></div>","PeriodicalId":39961,"journal":{"name":"Diagnostic Histopathology","volume":"32 10","pages":"Pages 638-653"},"PeriodicalIF":0.0000,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Diagnostic Histopathology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1756231726001325","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/7 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Adipocytic tumors are among the most common mesenchymal neoplasms in general surgical pathology. These tumors encompass a broad histological spectrum with variable degrees of adipocytic differentiation and a wide range of clinical behaviour, varying from entirely benign lipomas to aggressive pleomorphic liposarcomas. The World Health Organization (WHO) classification of adipocytic tumors has evolved considerably in the last decades, largely due to important advances in understanding their pathogenetic basis. Although classic examples of lipomas and liposarcomas are straightforward diagnoses, primarily distinguished by their morphological characteristics, several lipomatous tumors are now known to show unique, recurrent molecular genetic aberrations, identification of which can be used in the diagnostic work-up of distinct (uncommon) lipomatous tumor variants and histologically ambiguous adipocytic tumors. This article will provide a practical pattern-based approach to the histological diagnosis of benign, intermediate and malignant adipocytic neoplasms. We will focus on the currently known morphological, immunohistochemical and molecular features of the different adipocytic tumor entities, discuss their differential diagnoses and update on recently described adipocytic tumor entities (lipoblastoma-like tumor, atypical spindle cell/pleomorphic lipomatous tumor, and myxoid pleomorphic liposarcoma).
期刊介绍:
This monthly review journal aims to provide the practising diagnostic pathologist and trainee pathologist with up-to-date reviews on histopathology and cytology and related technical advances. Each issue contains invited articles on a variety of topics from experts in the field and includes a mini-symposium exploring one subject in greater depth. Articles consist of system-based, disease-based reviews and advances in technology. They update the readers on day-to-day diagnostic work and keep them informed of important new developments. An additional feature is the short section devoted to hypotheses; these have been refereed. There is also a correspondence section.