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镰状细胞性状的11岁男童骨样骨瘤的射频消融术:一例报告

Radiofrequency Ablation (RFA) for Osteoid Osteoma in an 11-Year-Old Male Child With Sickle Cell Trait: A Case Report.

作者信息

Nagaraju Nimmanagoti, Varma Ashish, Taksande Amar, Reddy Harshitha, Javvaji Chaitanya Kumar, Suryadevara Manasa, Reddy Naramreddy Sudheesh

机构信息

Pediatrics, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.

Internal Medicine, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research,, Wardha, IND.

出版信息

Cureus. 2024 Jul 1;16(7):e63626. doi: 10.7759/cureus.63626. eCollection 2024 Jul.

Abstract

Osteoid osteoma is a benign bone tumor that typically presents with nocturnal pain alleviated by nonsteroidal anti-inflammatory medications. The coexistence of osteoid osteoma with sickle cell anemia, a hereditary hemoglobinopathy characterized by vaso-occlusive crises and bone infarcts, poses diagnostic and therapeutic challenges due to overlapping clinical and radiological features. This condition primarily involves the long bones of the lower extremities, particularly the femur and tibia. Despite its benign nature, osteoid osteoma can significantly impact a patient's quality of life due to persistent and intense pain, often leading to substantial sleep disturbances and functional limitations.

摘要

骨样骨瘤是一种良性骨肿瘤,通常表现为夜间疼痛,非甾体类抗炎药可缓解。骨样骨瘤与镰状细胞贫血并存,镰状细胞贫血是一种遗传性血红蛋白病,其特征为血管阻塞性危机和骨梗死,由于临床和放射学特征重叠,给诊断和治疗带来了挑战。这种情况主要累及下肢长骨,尤其是股骨和胫骨。尽管骨样骨瘤本质上是良性的,但由于持续而剧烈的疼痛,它会显著影响患者的生活质量,常常导致严重的睡眠障碍和功能受限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e71c/11291688/68c029e9145e/cureus-0016-00000063626-i01.jpg

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