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眼眶胚胎性横纹肌肉瘤——病例报告

Embryonal rhabdomyosarcoma of orbit--a case report.

作者信息

Maurya O P, Patel R, Thakur V, Singh R, Kumar M

机构信息

Department of Ophthalmology, Institute of Medical Sciences, Banaras Hindu University, Varanas.

出版信息

Indian J Ophthalmol. 1990 Oct-Dec;38(4):202-4.

PMID:2086480
Abstract

Embryonal rhabdomyosarcoma of orbit presenting as a case of rapid proptosis of the right eye is reported in a 4 year old male child. There was no evidence of recurrence during a follow up of 6 months. Rhabdomyosarcoma is one of the most common primary malignant orbital neoplasms of child hood. It usually produces a precipitously progressing unilateral proptosis of sudden onset. It is a highly malignant neoplasm of pleuripotential embryonic mesoderm, which commonly differentiates to form cells similar to rhabdomyoblasts of the foetus. Because of the presence of elongated cells that contain abundance of eosinophilic glycogen rich cytoplasm, it is generally referred to as embryonal form of rhabdomyosarcoma.

摘要

本文报道了一名4岁男童,其眼眶胚胎性横纹肌肉瘤表现为右眼迅速突出。在6个月的随访中未发现复发迹象。横纹肌肉瘤是儿童最常见的原发性眼眶恶性肿瘤之一。它通常会导致单侧眼眶迅速进展性突出,且发病突然。它是一种源自多能胚胎中胚层的高度恶性肿瘤,通常分化形成类似于胎儿横纹肌母细胞的细胞。由于存在含有丰富嗜酸性糖原丰富细胞质的细长细胞,它通常被称为胚胎型横纹肌肉瘤。

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