Bone Metabolism of the Patient with a Malignant Melanoma during the Entry Examination and the Check-up of Whole-body Bone Scintigraphy
Language English Country Czech Republic Media print
Document type Case Reports, Journal Article
PubMed
27668530
DOI
10.14712/23362936.2016.14
PII: pmr_2016117020129
Knihovny.cz E-resources
- Keywords
- Beta-carboxyterminal cross-linked telopeptide of type I collagen, Bone scintigraphy, Human epididymis protein 4, Malignant melanoma, Osteocalcin,
- MeSH
- Collagen Type I blood MeSH
- Middle Aged MeSH
- Humans MeSH
- Melanoma blood pathology MeSH
- Biomarkers, Tumor blood MeSH
- Bone Neoplasms blood diagnostic imaging secondary MeSH
- Skin Neoplasms blood pathology MeSH
- Osteocalcin blood MeSH
- Peptides blood MeSH
- Radionuclide Imaging MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Names of Substances
- collagen type I trimeric cross-linked peptide MeSH Browser
- Collagen Type I MeSH
- Biomarkers, Tumor MeSH
- Osteocalcin MeSH
- Peptides MeSH
Malignant melanoma is a malignancy located predominantly in the skin and the incidence of melanoma increases. We compared the markers of bone metabolism - osteocalcin (OC), beta-carboxyterminal cross-linked telopeptide of type I collagen (β-CrossLaps, β-CTx) and tumour marker - human epididymis protein 4 (HE4) in the serum with finding during the entry examination and the check-up of whole-body bone scintigraphy of the patient with a malignant melanoma. Serum concentrations of OC, β-CTx, HE4 were determined in 1 patient (female, age 64 years) with malignant melanoma and correlated with the presence of equivocal bone metastases detected by whole-body bone scintigraphy (the entry examination and check-up after 6 months). Concentrations of bone metabolism markers decreased during six months and we observed progress in bone metastases. The change of the markers levels during the entry examination and the check-up of the whole-body bone scintigraphy with equivocal finding of bone metastases could be a sign of a possible initiating progression of malignant melanoma despite a clinically negative finding that does not prove the progression of the disease.
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