Adrenal metastasis of anaplastic meningioma: report of a rare case
Jazyk angličtina Země Polsko Médium print
Typ dokumentu kazuistiky, časopisecké články
PubMed
32337950
DOI
10.5114/fn.2019.91195
PII: 39386
Knihovny.cz E-zdroje
- Klíčová slova
- meningioma, rare tumours, metastasis,
- MeSH
- diferenciální diagnóza MeSH
- lidé středního věku MeSH
- lidé MeSH
- meningeální nádory diagnóza patologie MeSH
- meningeom diagnóza patologie MeSH
- mucin 1 genetika MeSH
- nádorové biomarkery analýza MeSH
- nádory nadledvin sekundární MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- Názvy látek
- MUC1 protein, human MeSH Prohlížeč
- mucin 1 MeSH
- nádorové biomarkery 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.
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