Abstract |
The case of a 4-month-old male infant treated with combined surgery and chemotherapy for an aggressive recurrent melanotic neuroectodermal tumor of infancy (MNTI) on the top of the alveolar process of the mandible with a long-term follow-up is presented. Initial treatment comprised conservative local excision and curettage of the mandible. After several local recurrences and because radical surgical excision would give gross functional and aesthetic mutilation, finally complete, long-lasting remission was achieved with adjuvant chemotherapy, according to a neuroblastoma protocol (10-year follow-up). The reason for this protocol was because molecular genetic studies of this tumor showed loss of heterozygosity of chromosome 1p and gain of chromosome 7q analogue to neuroblastomas. A combination of surgery and chemotherapy should be the preferred treatment in case of a recurrence MNTI because optimal functional and aesthetic outcome.
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Authors | Johannus Neven, Christine Hulsbergen-van der Kaa, Jacqueline Groot-Loonen, Peter C M de Wilde, Matthais A W Merkx |
Journal | Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics
(Oral Surg Oral Med Oral Pathol Oral Radiol Endod)
Vol. 106
Issue 4
Pg. 493-6
(Oct 2008)
ISSN: 1528-395X [Electronic] United States |
PMID | 18602297
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Vincristine
- Etoposide
- Carboplatin
- Ifosfamide
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Topics |
- Antineoplastic Combined Chemotherapy Protocols
(administration & dosage, therapeutic use)
- Carboplatin
(administration & dosage)
- Chemotherapy, Adjuvant
- Chromosomes, Human, Pair 1
- Chromosomes, Human, Pair 7
- Comparative Genomic Hybridization
- Etoposide
(administration & dosage)
- Humans
- Ifosfamide
(administration & dosage)
- Infant
- Loss of Heterozygosity
- Male
- Mandibular Neoplasms
(drug therapy, genetics, surgery)
- Neoplasm Recurrence, Local
- Neuroectodermal Tumor, Melanotic
(drug therapy, genetics, surgery)
- Vincristine
(administration & dosage)
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