Solitary Renal Myofibromatosis: An Unusual Cause of Infantile Hypertension

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چکیده

منابع مشابه

Spontaneous Remission of Solitary-Type Infantile Myofibromatosis

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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Solitary infantile myofibromatosis of the skull.

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.

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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: a cause of vertebra plana.

A 6-week-old boy was seen in the emergency department with progressive enlargement of head and neck masses. Bilateral periauricular masses had been present since birth and had undergone recent cervical extension. A mass of the right nasolabial fold had been present since 3 weeks of age. The lesions were asymptomatic and the infant was otherwise well. Computed tomography (CT) of the head and nec...

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Congenital 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: PEDIATRICS

سال: 1999

ISSN: 0031-4005,1098-4275

DOI: 10.1542/peds.103.5.e66