Infantile Myofibroma: Case Report and Review of the Literature.
CD34
infantile hemangiopericytoma
infantile myofibroma
solitary
Journal
Journal of Nippon Medical School = Nippon Ika Daigaku zasshi
ISSN: 1347-3409
Titre abrégé: J Nippon Med Sch
Pays: Japan
ID NLM: 100935589
Informations de publication
Date de publication:
08 Jan 2021
08 Jan 2021
Historique:
pubmed:
4
8
2020
medline:
2
2
2021
entrez:
4
8
2020
Statut:
ppublish
Résumé
We report a case of solitary infantile myofibroma (IM) with partially CD34-positive neoplastic cells on the back of a newborn boy. Ultrasonography showed a multilocular mass with a hypoechoic center surrounded by an isoechoic rim. Histopathological analysis revealed that the lesion was composed of small, round cells that were tightly packed and uniform. The cells had oval nuclei and were pale, CD34-positive, and richly cellular. They had interlacing fascicles of spindle cells with features of myofibroblasts with α-smooth muscle actin positivity. We speculate that neoplastic cells in most IMs differentiate towards myofibroblasts. However, in rare cases, their differentiation is more primitive and they express CD34, with or without α-smooth muscle actin expression.
Identifiants
pubmed: 32741901
doi: 10.1272/jnms.JNMS.2020_87-609
doi:
Substances chimiques
Antigens, CD34
0
Types de publication
Case Reports
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM