Literature DB >> 29449046

[Chordoma cutis, an unusual clinical presentation of a rare neoplasm: Chordoma].

Clémence Delteil1, Nausicaa Malissen2, Romain Appay3, Quentin Magis2, Sébastien Aubert4, Corinne Bouvier3, Marie-Aleth Richard2, Nicolas Macagno3.   

Abstract

Chordoma cutis represents an unusual clinical presentation of a rare neoplasm. The involvement of skin or sub-cutaneous soft tissues can be the consequence of local infiltration or metastasis; the latter may occur several years following the initial diagnosis of chordoma and therefore, may pose a diagnosis challenge when the clinical history of the patient is unknown. The clinical forms, morphology, immuno-histochemical profile and the main differential diagnoses of chordoma cutis are presented here through an anatomoclinical case.
Copyright © 2018 Elsevier Masson SAS. All rights reserved.

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Keywords:  Brachyury; Chordoma; Chordoma cutis; Chordome; Diagnostic différentiel; Differential diagnosis; Soft tissus; Tissus-mous

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Year:  2018        PMID: 29449046     DOI: 10.1016/j.annpat.2018.01.004

Source DB:  PubMed          Journal:  Ann Pathol        ISSN: 0242-6498            Impact factor:   0.407


  1 in total

1.  Metastatic chordoma.

Authors:  María Florencia Suarez Conde; Maria Gabriela Vallone; Virginia Mariana González; Felix Alberto Vigovich; Jose Gabriel Casas; Luciano Cermignan; Carlos Arturo Bas; Margarita Larralde
Journal:  JAAD Case Rep       Date:  2019-09-24
  1 in total

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