Cargando…

Concurrence of Congenital Muscular Torticollis and Congenital Torticollis Due to Other Anomalies: Two Case Reports

Introduction: Congenital muscular torticollis (CMT) is the most common cause of torticollis in infants; other causes, including osseous, ocular, and central nervous system torticollis can easily be overlooked. We report two rare cases of CMT with concurrent osseous or ocular torticollis. Case 1: A 1...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Min-Wook, Kim, Da-Ye, Lee, Dong-Woo, Ryoo, Da-Hye, Kim, Jaewon, Jang, Dae-Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8578520/
https://www.ncbi.nlm.nih.gov/pubmed/34778123
http://dx.doi.org/10.3389/fped.2021.709616
_version_ 1784596251110539264
author Kim, Min-Wook
Kim, Da-Ye
Lee, Dong-Woo
Ryoo, Da-Hye
Kim, Jaewon
Jang, Dae-Hyun
author_facet Kim, Min-Wook
Kim, Da-Ye
Lee, Dong-Woo
Ryoo, Da-Hye
Kim, Jaewon
Jang, Dae-Hyun
author_sort Kim, Min-Wook
collection PubMed
description Introduction: Congenital muscular torticollis (CMT) is the most common cause of torticollis in infants; other causes, including osseous, ocular, and central nervous system torticollis can easily be overlooked. We report two rare cases of CMT with concurrent osseous or ocular torticollis. Case 1: A 1-month-old female infant with a right neck mass and right-tilting head posture was referred. Neck ultrasonography showed diffuse hypertrophy and hyperechoic findings on the right sternocleidomastoid (SCM) muscle, which was consistent with right CMT. A clavicle X-ray imaging was conducted to identify an associated fracture due to birth trauma on the same day and a suspected congenital vertebral anomaly was coincidentally found. Subsequent three-dimensional computed tomography of the cervical spine showed a T1 hemivertebra causing the right-tilting head. The patient was diagnosed with the concurrent manifestation of CMT and congenital osseous torticollis. Case 2: A 3-month-old male infant with a 20° head tilt to the right with a limited cervical range of motion was referred. Neck ultrasonography showed a fibromatosis colli in the right SCM, suggesting CMT. He proceeded to physical therapy for seven months; however, there was little clinical improvement in his head and neck posture. The patient underwent an additional ophthalmologic examination and orbital magnetic resonance imaging (MRI) at 10 months of age. The result showed congenital agenesis of the left fourth cranial nerve with hypoplasia of the superior oblique muscle causing the right-tilting of the head. Ultimately, the boy was diagnosed with a concurrent manifestation of CMT and congenital ocular torticollis. Conclusion: Unless careful examinations are conducted, congenital vertebral anomalies and congenital agenesis of the fourth cranial nerve can go unnoticed in the present two cases. If a patient with CMT displays unusual features or does not respond to physical therapy, clinicians should consider not only a differential diagnosis but also concurrence with other causes of congenital torticollis.
format Online
Article
Text
id pubmed-8578520
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-85785202021-11-11 Concurrence of Congenital Muscular Torticollis and Congenital Torticollis Due to Other Anomalies: Two Case Reports Kim, Min-Wook Kim, Da-Ye Lee, Dong-Woo Ryoo, Da-Hye Kim, Jaewon Jang, Dae-Hyun Front Pediatr Pediatrics Introduction: Congenital muscular torticollis (CMT) is the most common cause of torticollis in infants; other causes, including osseous, ocular, and central nervous system torticollis can easily be overlooked. We report two rare cases of CMT with concurrent osseous or ocular torticollis. Case 1: A 1-month-old female infant with a right neck mass and right-tilting head posture was referred. Neck ultrasonography showed diffuse hypertrophy and hyperechoic findings on the right sternocleidomastoid (SCM) muscle, which was consistent with right CMT. A clavicle X-ray imaging was conducted to identify an associated fracture due to birth trauma on the same day and a suspected congenital vertebral anomaly was coincidentally found. Subsequent three-dimensional computed tomography of the cervical spine showed a T1 hemivertebra causing the right-tilting head. The patient was diagnosed with the concurrent manifestation of CMT and congenital osseous torticollis. Case 2: A 3-month-old male infant with a 20° head tilt to the right with a limited cervical range of motion was referred. Neck ultrasonography showed a fibromatosis colli in the right SCM, suggesting CMT. He proceeded to physical therapy for seven months; however, there was little clinical improvement in his head and neck posture. The patient underwent an additional ophthalmologic examination and orbital magnetic resonance imaging (MRI) at 10 months of age. The result showed congenital agenesis of the left fourth cranial nerve with hypoplasia of the superior oblique muscle causing the right-tilting of the head. Ultimately, the boy was diagnosed with a concurrent manifestation of CMT and congenital ocular torticollis. Conclusion: Unless careful examinations are conducted, congenital vertebral anomalies and congenital agenesis of the fourth cranial nerve can go unnoticed in the present two cases. If a patient with CMT displays unusual features or does not respond to physical therapy, clinicians should consider not only a differential diagnosis but also concurrence with other causes of congenital torticollis. Frontiers Media S.A. 2021-10-27 /pmc/articles/PMC8578520/ /pubmed/34778123 http://dx.doi.org/10.3389/fped.2021.709616 Text en Copyright © 2021 Kim, Kim, Lee, Ryoo, Kim and Jang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Kim, Min-Wook
Kim, Da-Ye
Lee, Dong-Woo
Ryoo, Da-Hye
Kim, Jaewon
Jang, Dae-Hyun
Concurrence of Congenital Muscular Torticollis and Congenital Torticollis Due to Other Anomalies: Two Case Reports
title Concurrence of Congenital Muscular Torticollis and Congenital Torticollis Due to Other Anomalies: Two Case Reports
title_full Concurrence of Congenital Muscular Torticollis and Congenital Torticollis Due to Other Anomalies: Two Case Reports
title_fullStr Concurrence of Congenital Muscular Torticollis and Congenital Torticollis Due to Other Anomalies: Two Case Reports
title_full_unstemmed Concurrence of Congenital Muscular Torticollis and Congenital Torticollis Due to Other Anomalies: Two Case Reports
title_short Concurrence of Congenital Muscular Torticollis and Congenital Torticollis Due to Other Anomalies: Two Case Reports
title_sort concurrence of congenital muscular torticollis and congenital torticollis due to other anomalies: two case reports
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8578520/
https://www.ncbi.nlm.nih.gov/pubmed/34778123
http://dx.doi.org/10.3389/fped.2021.709616
work_keys_str_mv AT kimminwook concurrenceofcongenitalmusculartorticollisandcongenitaltorticollisduetootheranomaliestwocasereports
AT kimdaye concurrenceofcongenitalmusculartorticollisandcongenitaltorticollisduetootheranomaliestwocasereports
AT leedongwoo concurrenceofcongenitalmusculartorticollisandcongenitaltorticollisduetootheranomaliestwocasereports
AT ryoodahye concurrenceofcongenitalmusculartorticollisandcongenitaltorticollisduetootheranomaliestwocasereports
AT kimjaewon concurrenceofcongenitalmusculartorticollisandcongenitaltorticollisduetootheranomaliestwocasereports
AT jangdaehyun concurrenceofcongenitalmusculartorticollisandcongenitaltorticollisduetootheranomaliestwocasereports