Spinal Canal Involvement in Solitary Infantile Myofibromatosis: Case Report
نویسندگان
چکیده
منابع مشابه
Solitary infantile myofibromatosis: report of two cases.
Infantile myofibromatosis (IM) is an unusual tumor of infancy and early childhood. It typically presents as a solitary or multicentric nodular mass involving skin, soft tissue, bone, or viscera. We describe 2 cases of solitary infantile myofibromatosis (IM) of the soft tissue with typical light microscopic features. The first is a 7-month-old boy who had a rapidly growing tumor of the right thi...
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Infantile myofibromatosis is a rare fibrous tumor of infancy. The cutaneous solitary type has typically an excellent prognosis. However, histologically, it is important to rule out leiomyosarcoma, which has a poor prognosis. The low frequency of mitosis was definitive for a diagnosis of infantile myofibromatosis. We present a cutaneous solitary-type case of infantile myofibromatosis. Following ...
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This is the report of a 6 months old boy presenting with a firm, solitary mass on the temporal region, associated with lysis of local bone. Investigations lead to a diagnosis of infantile myofibromatosis (IM). Wide local excision was performed. At one year follow-up, no recurrence was noted.
متن کاملCT of infantile myofibromatosis of the orbit with intracranial involvement: a case report.
An infant boy presented at birth with a large mass protruding from the left orbit that significantly displaced the left globe laterally and inferiorly . Biopsy of the mass was performed the next day, yielding the diagnosis of infantile myofibromatosis. Therapy was considered but the parents opted for no treatment, although they agreed to yearly CT follow-up examinations. The CT study at the tim...
متن کاملCongenital occurrence of solitary infantile myofibromatosis of the spleen.
Infantile myofibromatosis (IM) is a rare soft tissue tumor of infancy and childhood. We report the case of a newborn girl with an abdominal tumor discovered at 32 weeks of gestation by fetal ultrasound. She underwent a laparotomy for an unexplained abdominal mass 20 days after birth. The tumor originated from the spleen and was removed by splenectomy. There were no other abnormal findings on di...
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ژورنال
عنوان ژورنال: Indian Journal of Neurosurgery
سال: 2017
ISSN: 2277-954X,2277-9167
DOI: 10.1055/s-0036-1596041