Malignant granular cell tumor of the median nerve: a case report with a literature review of 157 cases.
Granular cell tumor
Malignant granular cell tumor
Median nerve
Nerve sheath tumor
Journal
Skeletal radiology
ISSN: 1432-2161
Titre abrégé: Skeletal Radiol
Pays: Germany
ID NLM: 7701953
Informations de publication
Date de publication:
Feb 2019
Feb 2019
Historique:
received:
01
04
2018
accepted:
18
06
2018
revised:
15
06
2018
pubmed:
8
7
2018
medline:
25
1
2019
entrez:
8
7
2018
Statut:
ppublish
Résumé
Malignant granular cell tumors are an extremely rare, high-grade sarcoma with a schwannian phenotype and are composed of malignant granular cells with cytoplasmic lysosomal inclusion. To date, 157 cases of malignant granular cell tumors have been reported. We report the first case of a malignant granular cell tumor arising from the digital nerve to the median nerve in the palm, and we review the 157 previously reported cases and summarize the clinical profile, treatment, and outcome of this tumor. The median age, tumor size, and follow-up periods were 51 years, 6 cm, and 24 months respectively. With respect to the oncological result, 53 patients (33.8%) had no evidence for disease, 31 (19.7%) were alive with the disease, and 51 (32.5%) died because of the disease. Our case report indicates that rare malignant tumors can arise from the digital nerve to the median nerve in the palm, an anatomical site that is usually affected by benign lesions. Exhaustive discussions between surgeons and pathologists are necessary for the treatment of this rare malignant tumor.
Identifiants
pubmed: 29980826
doi: 10.1007/s00256-018-3017-2
pii: 10.1007/s00256-018-3017-2
doi:
Substances chimiques
Contrast Media
0
Types de publication
Case Reports
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
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