Author/Authors :
Hajialiloo Sami, Sam Bone and Joint Reconstruction Research Center - Shafa Yahyaian Hospital - Iran University of Medical Sciences, Tehran, Iran , Zandrahimi, Farshad Bone and Joint Reconstruction Research Center - Shafa Yahyaian Hospital - Iran University of Medical Sciences, Tehran, Iran , Heidarikhoo, Mohamad Reza Bone and Joint Reconstruction Research Center - Shafa Yahyaian Hospital - Iran University of Medical Sciences, Tehran, Iran , Zahmatkesh, Mahsa Bone and Joint Reconstruction Research Center - Shafa Yahyaian Hospital - Iran University of Medical Sciences, Tehran, Iran , Karimi, Mansour Bone and Joint Reconstruction Research Center - Shafa Yahyaian Hospital - Iran University of Medical Sciences, Tehran, Iran , Gholampour, Hossein Bone and Joint Reconstruction Research Center - Shafa Yahyaian Hospital - Iran University of Medical Sciences, Tehran, Iran
Abstract :
Infantile fibrosarcoma is a rare soft-tissue neoplasm, which may render a diagnostic challenge
leading to misdiagnosis and consequently an inappropriate treatment of patients. This study
reports a case of infantile fibrosarcoma that mimicked a hemangioma in an 11-month-old girl. As
the lesion signal in the MRI was not consistent with the diagnosis of hemangiomas, we performed
a core needle biopsy, which its result was consistent with the diagnosis of infantile fibrosarcoma.
The lesion was initially treated with surgical resection. However, the lesion recurred one year after
the surgery. The recurrence was managed with debulking surgery. The fifth finger was necrotized
during the hospitalization after the relapse surgery. Finally, the necrotic finger was amputated.
Also, adjuvant chemotherapy was used to prevent further relapses. The 1-year follow-up of the
patient was recurrence-free. These findings highlight the importance of considering infantile
fibrosarcoma when an infant presents with a lesion that clinicaly mimics a vascular lesion.