Infantile Myofibroma: Case Report and Review of the Literature.


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
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

Pagination

355-358

Auteurs

Azusa Ogita (A)

Department of Dermatology and Dermatopathology, Nippon Medical School Musashi Kosugi Hospital.

Shin-Ichi Ansai (SI)

Department of Dermatology and Dermatopathology, Nippon Medical School Musashi Kosugi Hospital.

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Classifications MeSH