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Cytodiagnosis of sternocleidomastoid tumor of infancy

Sterocleidomastoid tumor of infancy (SCMI), also known as fibromatosis colli of infancy, is a benign, self limiting disease of new born characterised by its classical history and clinical presentation of firm to hard fusiform mass in the lower and middle portion of sternocleidomastoid. SCMI often ap...

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Autores principales: Baisakh, Manas R, Mishra, Minakshi, Narayanan, Radhika, Mohanty, Rajesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391802/
https://www.ncbi.nlm.nih.gov/pubmed/22787302
http://dx.doi.org/10.4103/0970-9371.97164
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author Baisakh, Manas R
Mishra, Minakshi
Narayanan, Radhika
Mohanty, Rajesh
author_facet Baisakh, Manas R
Mishra, Minakshi
Narayanan, Radhika
Mohanty, Rajesh
author_sort Baisakh, Manas R
collection PubMed
description Sterocleidomastoid tumor of infancy (SCMI), also known as fibromatosis colli of infancy, is a benign, self limiting disease of new born characterised by its classical history and clinical presentation of firm to hard fusiform mass in the lower and middle portion of sternocleidomastoid. SCMI often appears during early perinatal period between second to fourth weeks of life. A well recognized association between SCMI and primiparous birth, breech presentation, prolonged difficult labor and forceps deliveries is found. Cytology shows spindle shaped mature fibroblastic cells scattered singly along with degenerated and multinucleated giant muscle cells in a clean background. It is important to differentiate this lesion from different forms of infantile fibromatosis. Fine-needle aspiration cytology (FNAC), as a time saving, rapid and reliable diagnostic procedure, has got bigger role to play in reassurance of anxious parents, guiding for conservative management and avoiding surgery.
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spelling pubmed-33918022012-07-11 Cytodiagnosis of sternocleidomastoid tumor of infancy Baisakh, Manas R Mishra, Minakshi Narayanan, Radhika Mohanty, Rajesh J Cytol Case Report Sterocleidomastoid tumor of infancy (SCMI), also known as fibromatosis colli of infancy, is a benign, self limiting disease of new born characterised by its classical history and clinical presentation of firm to hard fusiform mass in the lower and middle portion of sternocleidomastoid. SCMI often appears during early perinatal period between second to fourth weeks of life. A well recognized association between SCMI and primiparous birth, breech presentation, prolonged difficult labor and forceps deliveries is found. Cytology shows spindle shaped mature fibroblastic cells scattered singly along with degenerated and multinucleated giant muscle cells in a clean background. It is important to differentiate this lesion from different forms of infantile fibromatosis. Fine-needle aspiration cytology (FNAC), as a time saving, rapid and reliable diagnostic procedure, has got bigger role to play in reassurance of anxious parents, guiding for conservative management and avoiding surgery. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3391802/ /pubmed/22787302 http://dx.doi.org/10.4103/0970-9371.97164 Text en Copyright: © Journal of Cytology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Baisakh, Manas R
Mishra, Minakshi
Narayanan, Radhika
Mohanty, Rajesh
Cytodiagnosis of sternocleidomastoid tumor of infancy
title Cytodiagnosis of sternocleidomastoid tumor of infancy
title_full Cytodiagnosis of sternocleidomastoid tumor of infancy
title_fullStr Cytodiagnosis of sternocleidomastoid tumor of infancy
title_full_unstemmed Cytodiagnosis of sternocleidomastoid tumor of infancy
title_short Cytodiagnosis of sternocleidomastoid tumor of infancy
title_sort cytodiagnosis of sternocleidomastoid tumor of infancy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391802/
https://www.ncbi.nlm.nih.gov/pubmed/22787302
http://dx.doi.org/10.4103/0970-9371.97164
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