Clinical Cancer Investigation Journal

CASE REPORT
Year
: 2016  |  Volume : 5  |  Issue : 4  |  Page : 356--358

Sternocleidomastoid tumor – rare infantile neck mass diagnosed by fine-needle aspiration cytology: Report of two cases


Shilpa Bairwa, Ashok Sangwaiya, Shivani Kalhan, Rahul Narayan Satarkar, Pawan Singh, Sonia Hasija 
 Department of Pathology, Shaheed Hasan Khan Mewati Government Medical College, Mewat, Haryana, India

Correspondence Address:
Shilpa Bairwa
Department of Pathology, Shaheed Hasan Khan Mewati Government Medical College, Nalhar, Mewat - 122 107, Haryana
India

Sternocleidomastoid tumor, also known as fibromatosis colli, is a rare form of fibromatosis in infants which is a rare, benign, and self-limiting tumor of infancy presenting as a well-circumscribed, hard, immobile, and fusiform swelling in the lower or middle portion of the sternocleidomastoid muscle. Birth injury associated with difficult labor is the most favored hypothesis. We describe using two cases as an example how this condition can be diagnosed by careful clinical history taking and fine-needle aspiration cytology so to avoid the surgical intervention. Here, we highlighted the cytological features of the sternocleidomastoid tumor so that it can be easily differentiated from congenital, inflammatory, and neoplastic masses in the neck in an infant.


How to cite this article:
Bairwa S, Sangwaiya A, Kalhan S, Satarkar RN, Singh P, Hasija S. Sternocleidomastoid tumor – rare infantile neck mass diagnosed by fine-needle aspiration cytology: Report of two cases.Clin Cancer Investig J 2016;5:356-358


How to cite this URL:
Bairwa S, Sangwaiya A, Kalhan S, Satarkar RN, Singh P, Hasija S. Sternocleidomastoid tumor – rare infantile neck mass diagnosed by fine-needle aspiration cytology: Report of two cases. Clin Cancer Investig J [serial online] 2016 [cited 2020 Jun 4 ];5:356-358
Available from: http://www.ccij-online.org/article.asp?issn=2278-0513;year=2016;volume=5;issue=4;spage=356;epage=358;aulast=Bairwa;type=0