Adrenal metastasis of anaplastic meningioma: report of a rare case
Language English Country Poland Media print
Document type Case Reports, Journal Article
PubMed
32337950
DOI
10.5114/fn.2019.91195
PII: 39386
Knihovny.cz E-resources
- Keywords
- meningioma, rare tumours, metastasis,
- MeSH
- Diagnosis, Differential MeSH
- Middle Aged MeSH
- Humans MeSH
- Meningeal Neoplasms diagnosis pathology MeSH
- Meningioma diagnosis pathology MeSH
- Mucin-1 genetics MeSH
- Biomarkers, Tumor analysis MeSH
- Adrenal Gland Neoplasms secondary MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Names of Substances
- MUC1 protein, human MeSH Browser
- Mucin-1 MeSH
- Biomarkers, Tumor MeSH
Meningiomas are the most common primary extra-axial tumours of the central nervous system, however their metastatic spread beyond central nervous system is rare. Here we present the case of a 54-year-old male with anaplastic meningioma who, 1.5 years after initial diagnosis, developed a tumorous expansion in his left adrenal gland, showing octreotide uptake on scintigraphy. Clinical diagnosis of pheochromocytoma was made and left adrenalectomy performed. The tumour weighed 480 grams and measured up to 140 mm in diameter. On histologic examination, morphology consistent with the diagnosis of anaplastic meningioma was present, resembling the original central nervous system tumour. The tumour expressed strongly SSTR2A and focally epithelial membrane antigen, p63 and pancytokeratin (AE1/3). An extensive panel of neuronal and additional epithelial markers (SOX10, synaptophysin, chromogranin, inhibin, calretinin, BER-EP4, MOC31) was negative. The review of the literature on meningioma metastasising outside the central nervous system and on its differential diagnosis is provided.
References provided by Crossref.org