Mediastinal malignant rhabdoid tumor in an infant: A rare case report. 2024

Elham Zarei, and Omid Alemohamad, and Zahra Rahimi, and Ali Manafi Anari, and Behzad Haghighi Aski, and Nafise Mortazavi, and Maryam Sakhaei, and Golnaz Gharebaghi, and Amir Ghadipasha
Hazrat Ali Asghar Children Hospital, Iran University of Medical Sciences, Tehran, Iran.

Mediastinal malignant rhabdoid tumor (MRT) is an exceedingly rare and aggressive neoplasm, particularly uncommon in infants. We present the case of a previously healthy 7-month-old male infant with mediastinal MRT. The patient initially presented with left eyelid ptosis and was otherwise asymptomatic. Initial investigations, including brain MRI, yielded unremarkable results, and the infant was discharged with vitamin B supplements. However, he was readmitted a week later with prolonged fever, poor feeding, diarrhea, and respiratory distress. Despite an initial diagnosis of bronchiolitis/viral respiratory tract infection, the patient's condition rapidly deteriorated. Subsequent evaluation revealed mediastinal MRT as the underlying cause. This case underscores the diagnostic challenges associated with mediastinal MRT in infants and highlights the importance of considering rare neoplastic etiologies in atypical clinical presentations.

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