在资源匮乏的环境中为一名 8 岁患者选择眼眶横纹肌肉瘤宽切手术:病例报告。

IF 0.5 Q4 OPHTHALMOLOGY
Case Reports in Ophthalmology Pub Date : 2024-10-25 eCollection Date: 2024-01-01 DOI:10.1159/000541645
Vera Sumual
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引用次数: 0

摘要

导读:横纹肌肉瘤是 5-8 岁儿童最常见的骨骼肌母细胞样肿瘤:横纹肌肉瘤是5-8岁儿童最常见的骨骼肌母细胞样肿瘤。它通常发生在头部、颈部、泌尿生殖道、腹膜后和四肢:病例介绍:一名 8 岁男孩诉说,过去 4 年来,他一直感觉左眼下方有一个肿块。起初肿块很小,后来逐渐变大,但没有伴随红肿、疼痛、瘙痒或眼球运动障碍等症状,也没有外伤史。经测量,左眼视力为 6/15,针孔矫正后视力提高到 6/6,右眼视力为 6/6。双眼眼压均为 15 毫米汞柱。左眼前段检查显示,下眼睑有一肿块,质地较硬,无红斑,无压痛,表面平坦,不能移动,结膜、角膜、瞳孔和晶状体各方面均正常。对比计算机断层扫描显示,肿块为实性,大小为 2.1 × 1.9 × 1.9 厘米,提示为左下眼睑肿块。患者在全身麻醉下接受了肿瘤切除手术。组织病理学检查确诊为胚胎性横纹肌肉瘤。患者被安排接受化疗:结论:眼眶横纹肌肉瘤通常表现为突然发病和迅速突眼,无外伤或呼吸道感染病史。胚胎亚型是最常见的,采用手术、化疗和放疗等综合治疗预后较好。在资源匮乏的环境中,早期临床怀疑和彻底的身体检查至关重要,因为医疗工具的有限性会使治疗复杂化。应根据现有资源调整治疗方法,定期随访对监测疗效和确保最佳治疗至关重要。应仔细检查儿童的任何肿胀,以便及早发现并进行有效干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Wide-Excision Choice in Orbital Rhabdomyosarcoma on an 8-Year-Old Patient in a Low-Resource Setting: A Case Report.

Introduction: Rhabdomyosarcoma is the most common neoplasm of skeletal myoblast-like cells in children aged 5-8 years. It typically occurs in the head, neck region, genitourinary tract, retroperitoneum, and extremities.

Case presentation: An 8-year-old boy complained of a lump under his left eye that he had felt for the past 4 years. Initially small, it gradually grew larger although there were no accompanying symptoms of redness, pain, itching, or eye movement disorders, and no history of trauma. Visual acuity in the left eye was measured at 6/15, with pinhole correction improving to 6/6, while the right eye was 6/6. Intraocular pressure in both eyes was 15 mm Hg. Anterior segment examination of the left eye revealed a mass on the lower eyelid with hard consistency, no erythema, no tenderness, with a flat surface, immobility, and all aspects of the conjunctiva, cornea, pupil, and lens appearing normal. A contrast computed tomography scan showed a solid mass measuring 2.1 × 1.9 × 1.9 cm, suggesting a left inferior eyelid mass. The patient underwent surgical excision of the tumor under general anesthesia. Histopathological examination confirmed the diagnosis of embryonal rhabdomyosarcoma. The patient was scheduled for chemotherapy.

Conclusions: Orbital rhabdomyosarcoma typically presents with sudden onset and rapid proptosis, without a history of trauma or respiratory tract infections. The embryonal subtype is the most common and has a better prognosis with combined therapy including surgery, chemotherapy, and radiation. In low-resource settings, early clinical suspicion and thorough physical examination are vital, as limited access to medical tools can complicate management. Treatment should be adapted based on available resources, and regular follow-up is essential to monitor outcomes and ensure optimal care. Any swelling in children should be carefully examined for early detection and effective intervention.

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来源期刊
CiteScore
0.90
自引率
0.00%
发文量
129
审稿时长
12 weeks
期刊介绍: This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of ophthalmology, including prevention, diagnosis, treatment, toxicities of therapy, supportive care, quality-of-life, and survivorship issues. The submission of negative results is strongly encouraged. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed. The intent of the journal is to provide clinicians and researchers with a tool to disseminate their personal experiences to a wider public as well as to review interesting cases encountered by colleagues all over the world. Universally used terms can be searched across the entire growing collection of case reports, further facilitating the retrieval of specific information. Following the open access principle, the entire contents can be retrieved at no charge, guaranteeing easy access to this valuable source of anecdotal information at all times.
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