Literature DB >> 29290323

[Dendritic infraclavicular fibromyxolipoma: At the boundary between spindle cell lipoma and solitary fibrous tumour].

Inmaculada Ruiz Molina1, Eduardo Solís García2, Vicente Cívico Amat2.   

Abstract

Dendritic fibromyxolipoma (DFML) is a rare soft tissue tumor recently described with only 27 cases reported in the literature. None of them have shown recurrence or metastasis after excision. Histologically it is composed of small stellate or spindle cells in a myxoid stroma with abundant collagen bundles mixed with mature adipose tissue. The proliferating cells typically show immunoexpression positive for CD34 and bcl-2. A cytogenetic analysis reveals deletion involving 13q14.3 region. We describe the first reported case to date located in the infraclavicular region. A 69 year old male with a painless mass well circumscribed and 5cm in size of several years of evolution, that after excision (2 years ago) he has not shown signs of recurrence or metastasis. This study reflects the clinicopathological features, differential diagnosis and a review of the literature of the DFML.
Copyright © 2017 Sociedad Española de Anatomía Patológica. Publicado por Elsevier España, S.L.U. All rights reserved.

Entities:  

Keywords:  Dendritic fibromyxolipoma; Fibromixolipoma dendrítico; Lipoma de células fusiformes mixoide; Myxoid spindle cell lipoma; Solitary fibrous tumor; Tumor fibroso solitario

Mesh:

Year:  2017        PMID: 29290323     DOI: 10.1016/j.patol.2016.12.007

Source DB:  PubMed          Journal:  Rev Esp Patol        ISSN: 1699-8855


  1 in total

1.  Dendritic fibromyxolipoma: A case report.

Authors:  Hongyun Liu; Shumin Hei; Jigang Wang; Qiliang Zhang; Xinjuan Yu; Hua Chen
Journal:  Mol Clin Oncol       Date:  2020-11-12
  1 in total

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