一名成人患者的多层椎体骨坏死:一个罕见病例及文献综述

Q3 Medicine
Sonal Saran, Akash Rauniyar, Bhumireddy Vijaya Madhuri, Pooja Kundu
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引用次数: 0

摘要

骨坏死的特点是缺血性骨损伤导致细胞死亡和骨吸收,由于放疗和药物等多种病因,骨坏死表现在不同的解剖部位。股骨头和颌骨等某些部位的骨坏死已引起人们的关注,但椎体骨坏死的研究仍较少,也缺乏标准化的分类系统。本报告介绍了一例独特的病例,一名52岁的女性患者因弥漫大B细胞淋巴瘤接受化疗,出现多发性椎体骨坏死,这在英文医学文献中十分罕见。患者出现发热、腹痛和淋巴恶性肿瘤标志物,开始接受利妥昔单抗、环磷酰胺、长春新碱和泼尼松龙(R-CVP)方案化疗。治疗期间,她出现了呼吸困难和背痛,影像学检查显示她的多节椎骨和其他骨骼部位出现了广泛的骨坏死。化疗、人类免疫缺陷病毒(HIV)治疗、创伤等各种因素都会导致椎体坏死。虽然淋巴瘤患者骨坏死的情况很少见,但化疗引起的骨髓坏死可导致骨骼受累。由于血液供应有限,椎体,尤其是椎体前部,很容易受到影响。X线片上出现椎体内真空裂隙是骨坏死的先兆,而磁共振成像(MRI)可显示低密度区和积液。本病例强调了诊断和处理多级椎体骨坏死的复杂性,而标准化方案的缺乏又加剧了这一复杂性。疾病过程和治疗方式之间的相互作用使决策变得更加复杂,强调了进一步研究制定最佳诊断和治疗指南的必要性。总之,本病例揭示了淋巴瘤患者骨坏死的一种罕见表现,强调了诊断和管理方面的挑战。有必要开展进一步的研究,以加深对这一使人衰弱的疾病的理解并改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multilevel Vertebral Body Osteonecrosis in an Adult Patient: A Rare Case with Review of Literature.

Osteonecrosis, characterized by ischemic bone injury leading to cell death and bone resorption, manifests in various anatomical sites due to multiple etiologies such as radiotherapy and medications. While certain sites like the femoral head and jaw have garnered attention, vertebral body osteonecrosis remains less explored and lacks a standardized classification system. This report presents a unique case of a 52-year-old woman undergoing chemotherapy for diffuse large B-cell lymphoma who developed multilevel vertebral body osteonecrosis, a rare occurrence in English medical literature. The patient presented with fever, abdominal pain, and lymphoid malignancy markers, initiating chemotherapy with the rituximab, cyclophosphamide, vincristine, and prednisolone (R-CVP) regimen. During treatment, she experienced breathing difficulties and back pain, prompting imaging studies revealing extensive osteonecrosis affecting multiple vertebrae and other skeletal sites. Various factors, including chemotherapy, human immunodeficiency virus (HIV) therapy, trauma, and others, contribute to vertebral body necrosis. While osteonecrosis in lymphoma patients is rare, chemotherapy-induced marrow necrosis can lead to bone involvement. Vertebral bodies, especially their anterior portions, are susceptible due to limited blood supply. The presence of an intravertebral vacuum cleft on radiographs is pathognomonic for osteonecrosis, while magnetic resonance imaging (MRI) reveals hypointense areas and fluid collections. This case underscores the complexity of diagnosing and managing multilevel vertebral body osteonecrosis, exacerbated by the lack of standardized protocols. The interplay between disease processes and treatment modalities complicates decision-making, emphasizing the need for further research to establish optimal diagnostic and treatment guidelines. In conclusion, this case sheds light on a rare manifestation of osteonecrosis in a lymphoma patient, highlighting the challenges in diagnosis and management. Further research is warranted to enhance understanding and improve outcomes for patients with this debilitating condition.

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