Recurrent primary endobronchial fetal rhabdomyoma: a case report and literature review.
benign mesenchymal neoplasm
endobronchial
fetal rhabdomyoma
recurrence
skeletal muscle differentiation
Journal
Pathologica
ISSN: 1591-951X
Titre abrégé: Pathologica
Pays: Italy
ID NLM: 0401123
Informations de publication
Date de publication:
Dec 2021
Dec 2021
Historique:
received:
05
09
2020
accepted:
14
12
2020
entrez:
2
1
2022
pubmed:
3
1
2022
medline:
5
1
2022
Statut:
ppublish
Résumé
Fetal rhabdomyoma is an extremely rare benign rhabdomyoblastic tumor with myotube-like differentiation, mainly arising on mucosal surfaces of the head and neck region of both children and young patients, almost invariably definitively treated with surgical excision. Herein the case of a male adult suffering from a recurrent fetal rhabdomyoma primary involving the bronchial structures is reported, along with a detailed literature review. This is the first fetal rhabdomyoma described to originate in such a localization; furthermore, an 11-year interval period between the first lesion and the recurrent one has never been reported.
Identifiants
pubmed: 34974549
doi: 10.32074/1591-951X-197
pmc: PMC8720399
doi:
Types de publication
Case Reports
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
436-441Informations de copyright
Copyright © 2021 Società Italiana di Anatomia Patologica e Citopatologia Diagnostica, Divisione Italiana della International Academy of Pathology.
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