Every Posterior Fossa Mass Is Not a Tumor— Rare Case Report of Isolated Intracranial Infantile Myofibromatosis
نویسندگان
چکیده
منابع مشابه
Infantile myofibromatosis : report of a rare disease *
The pathogenesis of generalized fibromatosis still remains unknown, despite reports on association with estrogen receptors. This disease is classified into three types as follows: solitary fibromatosis, congenital generalized fibromatosis without visceral involvement, and congenital generalized fibromatosis with both cutaneous and visceral involvement. In most cases, the disease is sporadic, bu...
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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...
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Received March 29, 2003 Abstract Congenital infantile myofibromatosis is a rare disorder with multiple fibromatous tumours in skin, bone, muscle, viscera and subcutaneous tissue presenting in early infancy. Multiple lytic bone lesions and vertebra involvement are also common, mimicking the clinical picture of metastatic tumours. However, it is a disease with variable prognosis depending on the ...
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A 57-year-old woman with a history of hypothyroidism, hysterectomy and depression presented to the emergency department (ED) with 3 months of progressive vertigo, ataxia and posterior headache. The patient denied fever, weight loss, vision difficulty or trauma. The patient was directed to the ED because of an abnormal outpatient MRI done earlier that day obtained by her family physician. The pa...
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ژورنال
عنوان ژورنال: OALib
سال: 2014
ISSN: 2333-9705,2333-9721
DOI: 10.4236/oalib.1100670