Case report of granular cell myoblastoma arising within the medial rectus muscle.
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چکیده
منابع مشابه
Case report of granular cell myoblastoma arising within the medial rectus muscle.
A rare case of granular cell myoblastoma is reported in a 37-year-old man where the tumour was situated within the medial rectus muscle. Histological, cytochemical and ultrastructural examination showed it to have features typical of granular cell myoblastoma. It also reacted with chorioembryonic antigen antisera, a sign of primitive cell origin. The findings add further weight to the idea of t...
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Granular cell myoblastoma is a relatively uncommon lesion of debatable histogenesis, appearing as a small, solitary (but occasionally multiple) neoplasm and usually taking a benign course. The malignant counterpart has rarely been observed examples have also been found in virtually every organ or tissue of the body (Strong and others, I970), but only rarely in the orbit. Von Bahr (I938) reporte...
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A case of granular cell myoblastoma which metastasized with fatal results is described. The literature relating to similar cases is reviewed and a total of 13 acceptable cases is listed.
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Case Report A 24-year-old white woman was first seen in consultation in September, 1960, complaining of a "little vein" in the nasal side of the sclera of the right eye, which had been growing over a period of three months without symptoms, but three days previously she complained of sudden pain and "severe loss of vision". Examination.-Right eye: A salmon-pink solid mass was seen growing insid...
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Background: Granular cell tumor (Abrikossoff’s tumor) is a rare and slow-growing tumor of the soft tissue. Originated from the Schwann cells, it is often a benign tumor, but it can be malignant in 1-3% of the cases. Malignant cases can cause significant morbidity and mortality. It may develop in many anatomic locations, especially in the head and neck region, and also in skin and subcutaneous t...
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ژورنال
عنوان ژورنال: British Journal of Ophthalmology
سال: 1983
ISSN: 0007-1161
DOI: 10.1136/bjo.67.1.17