Melanotic neuroectodermal tumor of infancy

Other names: MNTI
A bone resection sample showing the pigmentation below the surface in a melanotic neuroectodermal tumor of infancy

Melanotic neuroectodermal tumor of infancy is a very rare oral cavity tumor that is seen in patients usually at or around birth. It must be removed to be cured. Definitions: A rare, biphasic, neuroblastic, and pigmented epithelial neoplasm of craniofacial sites, usually involving the oral cavity or gums.

## Contents

* 1 Signs and symptoms
* 2 Pathogenesis
* 3 Diagnosis
* 3.1 Macroscopic
* 3.2 Microscopic
* 3.3 Immunohistochemistry
* 3.4 Differential diagnoses
* 4 Management
* 5 Epidemiology
* 6 References
* 7 Further reading
* 8 External links

## Signs and symptoms[edit | edit source]

Clinical presentation of the condition originating in the mandible

Most patients present with a very rapidly growing mass that often gives a bluish appearance in the mouth. This is because the pigmentation in the cells appears blue through the overlying epithelium (mucosa).[1] By imaging studies, there is usually a large expansive radiolucent (clear) mass without well defined borders. Calcifications within the mass may be seen.[2] More than 70% involve the maxilla (usually maxillary anterior alveolar ridge), while the mandible and skull are affected less often.[2] There is often an elevated vanilmandelic acid level.[1][3][4]

## Pathogenesis[edit | edit source]

It is considered to be a developmental anomaly, and thus is congenital in presentation. It is thought to be derived from neural crest, which is one of the embryologic tissue types. The reason for this postulation is based on the expression of melanotransferrin (melanoma-specific peptide that may play role in iron metabolism).[1][2][4]

## Diagnosis[edit | edit source]

### Macroscopic[edit | edit source]

Usually there is a smooth, firm mass, with mottled white-gray to blue-black cut surfaces. The overall size ranges from 1–10 cm with a mean size 3.5 cm.[1][2]

### Microscopic[edit | edit source]

The tumor is usually very well circumscribed but not encapsulated. There are two cell types present (biphasic), arranged in alveolar or tubular configurations. There are centrally located, small, darkly staining cells comprising the majority of cells. These cells have a fibrillary cytoplasm surrounding round nuclei with coarse and heavy nuclear chromatin. These cells are surrounded by much larger polygonal cells that have open nuclear chromatin and abundant opaque cytoplasm that has granular melanin pigment. There is usually no hemorrhage, necrosis or increased mitoses.[1][4]

### Immunohistochemistry[edit | edit source]

The lesional cells will show cross reactivity with several different families of immunohistochemistry markers (polyphenotypic), including neural, melanocytic, and epithelial.

* Large tumor cells: Keratin, vimentin, HMB-45, NSE, CD57
* Small tumor cells: Synaptophysin, GFAP, NSE, CD57
* There is usually a variable expression of EMA and S100 protein.[4]

* A high power of melanotic neuroectodermal tumor of infancy showing pigmented large epithelioid cells and smaller primitive cells (hematoxylin and eosin stain).

* A high power of melanotic neuroectodermal tumor of infancy showing pigmented large epithelioid cells and smaller primitive cells in alveolar nests (hematoxylin and eosin stain).

### Differential diagnoses[edit | edit source]

It is important in this age group to exclude other tumors that can have a similar appearance, such as rhabdomyosarcoma, lymphoma, Ewing sarcoma (primitive neuroectodermal tumor), or even a melanoma (although they are very very rare in infants).[1][4]

## Management[edit | edit source]

Even though there is often a very dramatic and rapidly enlarging, destructive tumor, there is usually a benign clinical course after complete local excision (usually by partial maxillectomy) with clear or free surgical margins. In rare cases, chemotherapy may be used for recurrent or residual tumors. Overall, the outcome is good, although it is quite unpredictable, with about 30% of patients have a recurrence. In about 10% of cases, metastasis may be seen (lymph nodes, liver, bone and soft tissue).[1] [4]

## Epidemiology[edit | edit source]

This tumor is exception, with fewer than 500 cases reported world wide. More than 95% of patients are less than 1 year of age at presentation, with about 80% less than 6 months. Females are affected more often than males (2:1).[1][4]

## References[edit | edit source]

1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 Selim H, Shaheen S, Barakat K, Selim AA (June 2008). "Melanotic neuroectodermal tumor of infancy: review of literature and case report". J Pediatr Surg. 43 (6): E25–9. doi:10.1016/j.jpedsurg.2008.02.068. PMID 18558161.
2. ↑ 2.0 2.1 2.2 2.3 Nelson BL, Thompson LD (June 2006). "Melanotic neuroectodermal tumor of infancy". Ear Nose Throat J. 85 (6): 365. doi:10.1177/014556130608500608. PMID 16866106. S2CID 31516123.
3. ↑ Marston AP, Black A, Pambuccian SE, Hamlar DD (July 2014). "Mass originating from the maxillary alveolar crest in an infant". JAMA Otolaryngol Head Neck Surg. 140 (7): 667–8. doi:10.1001/jamaoto.2014.632. PMID 24810545.
4. ↑ 4.0 4.1 4.2 4.3 4.4 4.5 4.6 Gaiger de Oliveira M, Thompson LD, Chaves AC, Rados PV, da Silva Lauxen I, Filho MS (August 2004). "Management of melanotic neuroectodermal tumor of infancy". Ann Diagn Pathol. 8 (4): 207–12. doi:10.1053/j.anndiagpath.2004.04.003. PMID 15290671.

## Further reading[edit | edit source]

Lester D. R. Thompson; Bruce M. Wenig (2016). Diagnostic Pathology: Head and Neck, 2nd edition. Elsevier. ISBN 978-0323392556.

## External links[edit | edit source]

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* eMedicine: med/107941

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