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1.
Journal of the Korean Radiological Society ; : 420-424, 2022.
Artigo em Inglês | WPRIM | ID: wpr-926426

RESUMO

Fibrous hamartoma of infancy in the middle ear is extremely rare. We report the case of a 26-month-old male patient who presented with a mass in the left middle ear. A temporal bone CT scan showed complete opacification of the left middle ear and mastoid air cells without ossicular erosion. On MRI, the mass revealed heterogeneous signal intensities indicative of fat and fibrous components. A definitive diagnosis was made postoperatively based on the histological results. Although rare, fibrous hamartoma of infancy should be considered as a differential diagnosis of a middle ear mass during childhood.

2.
Journal of the Korean Radiological Society ; : 1497-1503, 2020.
Artigo em Inglês | WPRIM | ID: wpr-901286

RESUMO

Inflammatory myofibroblastic tumors (IMTs) are rare. They are characterized by myofibroblastic spindle cell proliferation with a varying degree of inflammatory cell infiltration. IMT can occur in any anatomic location but has been reported in the lung, mesentery, and omentum, mainly in children or young adults. It rarely occurs in the pancreas and is often difficult to distinguish from other tumors, including some malignant ones. Therefore, it can be challenging to make a radiological diagnosis of IMT. Here, we present a case of IMT that occurred in the pancreas head of a middle-aged female. The patient’s ultrasonography, computed tomography, and magnetic resonance imaging findings are presented along with a review of the literature.

3.
Journal of the Korean Radiological Society ; : 1497-1503, 2020.
Artigo em Inglês | WPRIM | ID: wpr-893582

RESUMO

Inflammatory myofibroblastic tumors (IMTs) are rare. They are characterized by myofibroblastic spindle cell proliferation with a varying degree of inflammatory cell infiltration. IMT can occur in any anatomic location but has been reported in the lung, mesentery, and omentum, mainly in children or young adults. It rarely occurs in the pancreas and is often difficult to distinguish from other tumors, including some malignant ones. Therefore, it can be challenging to make a radiological diagnosis of IMT. Here, we present a case of IMT that occurred in the pancreas head of a middle-aged female. The patient’s ultrasonography, computed tomography, and magnetic resonance imaging findings are presented along with a review of the literature.

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