Cytodiagnosis of chondroid syringoma-Series of three cases.
chondroid syringoma
chondromyxoid stroma
cutaneous mixed tumor
myoepithelial cells
Journal
Diagnostic cytopathology
ISSN: 1097-0339
Titre abrégé: Diagn Cytopathol
Pays: United States
ID NLM: 8506895
Informations de publication
Date de publication:
Sep 2021
Sep 2021
Historique:
revised:
19
05
2021
received:
17
12
2020
accepted:
02
06
2021
pubmed:
27
6
2021
medline:
4
1
2022
entrez:
26
6
2021
Statut:
ppublish
Résumé
Chondroid syringoma is a rare, benign, appendegeal neoplasm. It was initially termed as mixed tumor as it comprises both epithelial cells and chondromyxoid stroma. It usually presents as a slow growing, solitary, painless, subcutaneous, or intracutaneous mass, frequently in the head and neck region. Cytological features usually include the presence of both components, similar to histology but aspiration of only one component or atypical features can pose challenges in diagnosis. According to literature, only a few single case reports describing the cytological features of chondroid syringoma has been published. We report three cases of chondroid syringoma and its differential diagnosis on cytology.
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
E374-E377Informations de copyright
© 2021 Wiley Periodicals LLC.
Références
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