Every Posterior Fossa Mass Is Not a Tumor—Rare Case Report of Isolated Intracranial Infantile Myofibromatosis

Kishor Taori; Mansi Jain; Lalit Garg; Ajinky Patil; Jawhar Rathod; Rohit Khisti; Amit Disawal; Ramesh Parate; Shyam Chhadi

doi:10.4236/oalib.1100670

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OALibJ> Vol.1 No.4, July 2014

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Every Posterior Fossa Mass Is Not a Tumor—Rare Case Report of Isolated Intracranial Infantile Myofibromatosis

Abstract PP. 1-5

DOI: 10.4236/oalib.1100670 1,250 Downloads 1,485 Views

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Kishor Taori, Mansi Jain^*, Lalit Garg, Ajinky Patil, Jawhar Rathod, Rohit Khisti, Amit Disawal, Ramesh Parate, Shyam Chhadi

Affiliation(s)

Department of Radiodiagnosis, Government Medical College, Nagpur, India.

ABSTRACT

Infantile myofibromatosis is the most common fibrous disorder of infancy and early childhood. It can present in three forms—solitary lesion, multicentric with visceral involvement and multi-centeric without visceral involvement. Intracranial involvement is rare and when it occurs, it is generally extension of extracranial lesion into the intracranial compartment. Here we present a rare case of isolated posterior fossa involvement presenting clinically as congenital facial palsy.

KEYWORDS

Infantile Myofibromatosis, Posterior Fossa, Congenital Facial Palsy

Conflicts of Interest

The authors declare no conflicts of interest.

Cite this paper

Taori, K. , Jain, M. , Garg, L. , Patil, A. , Rathod, J. , Khisti, R. , Disawal, A. , Parate, R. and Chhadi, S. (2014) Every Posterior Fossa Mass Is Not a Tumor—Rare Case Report of Isolated Intracranial Infantile Myofibromatosis. Open Access Library Journal, 1, 1-5. doi: 10.4236/oalib.1100670.

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