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Melanotic Neuroectodermal Tumour of Infancy - A Case Report and Review of Literature
RATIONALE: Melanotic neuroectodermal tumour of infancy (MNTI) is universally described as a rare, benign, pigmented lesion which most frequently involves the maxilla. Its origin is well established to be in the neural crest cells. Due to the high recurrence rate and aggressive behaviour mimicking ma...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527851/ https://www.ncbi.nlm.nih.gov/pubmed/36199457 http://dx.doi.org/10.4103/ams.ams_5_22 |
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author | Jakka, Sabareesh Roy, Indranil Deb Rangan, Mohan Pandey, Satyanarayan Singh, Anup Kumar |
author_facet | Jakka, Sabareesh Roy, Indranil Deb Rangan, Mohan Pandey, Satyanarayan Singh, Anup Kumar |
author_sort | Jakka, Sabareesh |
collection | PubMed |
description | RATIONALE: Melanotic neuroectodermal tumour of infancy (MNTI) is universally described as a rare, benign, pigmented lesion which most frequently involves the maxilla. Its origin is well established to be in the neural crest cells. Due to the high recurrence rate and aggressive behaviour mimicking malignancy, it poses a great challenge in their diagnosis, treatment planning, and prognosis. PATIENT CONCERN: Two-year-old female with no known comorbidities was brought in with the chief complaint of a growing swelling in the upper lip region. DIAGNOSIS AND TREATMENT: She was taken up for resection of the tumour under general anaesthesia. The specimen was subjected to histological and immunological examination confirming the diagnosis of MNTI. OUTCOME: The postoperative period was uneventful. After regular follow-up, the patient showed satisfactory healing with no signs of recurrence. TAKE-AWAY LESSONS: Based on our experience, we feel that the diagnosis of MNTI is mainly clinical. Early conservative surgical excision and regular follow-up provide an excellent result with good prognosis. |
format | Online Article Text |
id | pubmed-9527851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-95278512022-10-04 Melanotic Neuroectodermal Tumour of Infancy - A Case Report and Review of Literature Jakka, Sabareesh Roy, Indranil Deb Rangan, Mohan Pandey, Satyanarayan Singh, Anup Kumar Ann Maxillofac Surg Case Report - Cyst and Tumours RATIONALE: Melanotic neuroectodermal tumour of infancy (MNTI) is universally described as a rare, benign, pigmented lesion which most frequently involves the maxilla. Its origin is well established to be in the neural crest cells. Due to the high recurrence rate and aggressive behaviour mimicking malignancy, it poses a great challenge in their diagnosis, treatment planning, and prognosis. PATIENT CONCERN: Two-year-old female with no known comorbidities was brought in with the chief complaint of a growing swelling in the upper lip region. DIAGNOSIS AND TREATMENT: She was taken up for resection of the tumour under general anaesthesia. The specimen was subjected to histological and immunological examination confirming the diagnosis of MNTI. OUTCOME: The postoperative period was uneventful. After regular follow-up, the patient showed satisfactory healing with no signs of recurrence. TAKE-AWAY LESSONS: Based on our experience, we feel that the diagnosis of MNTI is mainly clinical. Early conservative surgical excision and regular follow-up provide an excellent result with good prognosis. Wolters Kluwer - Medknow 2022 2022-08-16 /pmc/articles/PMC9527851/ /pubmed/36199457 http://dx.doi.org/10.4103/ams.ams_5_22 Text en Copyright: © 2022 Annals of Maxillofacial Surgery https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report - Cyst and Tumours Jakka, Sabareesh Roy, Indranil Deb Rangan, Mohan Pandey, Satyanarayan Singh, Anup Kumar Melanotic Neuroectodermal Tumour of Infancy - A Case Report and Review of Literature |
title | Melanotic Neuroectodermal Tumour of Infancy - A Case Report and Review of Literature |
title_full | Melanotic Neuroectodermal Tumour of Infancy - A Case Report and Review of Literature |
title_fullStr | Melanotic Neuroectodermal Tumour of Infancy - A Case Report and Review of Literature |
title_full_unstemmed | Melanotic Neuroectodermal Tumour of Infancy - A Case Report and Review of Literature |
title_short | Melanotic Neuroectodermal Tumour of Infancy - A Case Report and Review of Literature |
title_sort | melanotic neuroectodermal tumour of infancy - a case report and review of literature |
topic | Case Report - Cyst and Tumours |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527851/ https://www.ncbi.nlm.nih.gov/pubmed/36199457 http://dx.doi.org/10.4103/ams.ams_5_22 |
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