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Isolated infantile myofibroma of the calvarium: Report of a case with a literature review

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A Correction to this article was published on 10 February 2024

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Abstract

Objective

Infantile myofibromatosis is a rare entity of childhood characterized by benign myofibroblastic tumors in the soft tissues, the bones, and occasionally the viscera. Solitary skeletal lesions are relatively uncommon. Calvarial involvement should be distinguished from more aggressive tumors for appropriate treatment.

Methods

We reviewed solitary infantile myofibroma of the calvarium and discussed the relevant computed tomography and magnetic resonance imaging findings along with differential diagnosis. A case study of the frontal bone in a 5-month-old girl was also presented.

Results

Fourteen cases were reviewed, including the current case. Of the 13 cases with known sex, eight were male and five female. The mean age was 3.03 with an age range of 0.41–9 years. Nine of the 14 tumors were in the frontal bone. The lesions were intradiploic with tabula interna and/or externa of the calvaria involvement. The mean largest diameter was 22.3 mm. Upon computed tomography, all the lesions were expansile and lytic, and hypoattenuated, isoattenuated or occasionally hyperatenuated. Calcification was not seen. On magnetic resonance imaging, most neoplasms were hypointense on T1-weighted and T2-weighted images. Neoplasms showed hypointense signal on diffusion-weighted imaging and hyperintense on apparent diffusion coefficient, without restricted diffusion in three cases. All lesions were intensely enhanced after gadolinium administration. Treatment was total surgical resection and recurrence was not observed during follow-up.

Conclusions

Infantile myofibromas are rare, typically intradiploic expansile lytic lesions with tabula interna and/or externa involvement. Distinctive imaging features include the presence of hipointense signals on T2-weighted magnetic resonance images without restricted diffusion on diffusion-weighted imaging. A slow-growing, firm, painless, and nontender mass with supportive imaging findings should raise suspicion of the disease.

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Authors and Affiliations

Authors

Contributions

M.K.D., O.Y. and O.C. wrote the main manuscript. All authors prepared the figures and reviewed the main manuscript.

Corresponding author

Correspondence to Mustafa Kemal Demir.

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This article do not contain studies with animals by author.

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Informed consent was obtained from the patient’s parents included in the study.

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The original online version of this article was revised: In this article the author name "Ozgur Celik" was incorrectly written as "OzgurCelikj Celik" and the affiliation should be corrected to "Faculty of Medicine, Near East University, Nicosia, Cyprus".

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Demir, M., Yapicier, O., Celik, O. et al. Isolated infantile myofibroma of the calvarium: Report of a case with a literature review. Childs Nerv Syst 40, 1277–1284 (2024). https://doi.org/10.1007/s00381-024-06289-9

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