马德龙病病例报告及文献综述。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY Orphanet Journal of Rare Diseases Pub Date : 2024-08-17 DOI:10.1186/s13023-024-03303-w
Cheng Jiao, Wei Liu, Yiming Qiao, Shuai Qi, Yifei Shen
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引用次数: 0

摘要

背景:马德龙病(Madelung's disease,MD)又称良性对称性脂肪瘤病、多发性对称性脂肪瘤病或劳努瓦-本绍德综合征,是一种不常见的良性疾病,其特征是头、颈和躯干部位的脂肪组织对称性增生:本病例中,患者为女性,中年后期,被诊断为 I 型 MD。值得注意的是,她之前没有饮酒史,也没有家族遗传史。临床诊断后,患者接受了医学影像评估,以确定手术参数。术后,她的恢复情况良好,没有出现任何手术并发症:结果:患者成功接受了脂肪瘤肿块切除手术。结果:患者成功接受了脂肪瘤肿块切除手术,术后恢复顺利,没有出现任何并发症,随访 7 个月也没有发现复发:结论:及时诊断和早期手术干预对提高 MD 患者的生活质量至关重要。术前医学影像检查是非常有效的工具,有助于提高手术安全性,降低手术过程中出现并发症的概率。
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A case report on Madelung's disease and comprehensive review of the literature.

Background: Madelung's disease (MD), alternatively referred to as benign symmetric lipomatosis, multiple symmetric lipomatosis, or Launois-Bensaude syndrome, is an uncommon benign disorder marked by symmetric proliferation of adipose tissue in the head, neck, and torso regions.

Case description: In this case, the patient was a female with the late middle-aged demographic, diagnosed with Type I MD. Notably, she exhibited no prior history of alcohol consumption, and there was no family history of MD. Subsequent to the clinical diagnosis, the patient underwent medical imaging assessments to delineate the surgical parameters. Post-surgery, she demonstrated a favorable recovery trajectory, marked by the absence of any surgical complications.

Result: The patient underwent successful surgical excision of the lipomatous mass. Postoperatively, she had an uneventful recovery with no complications and no recurrence observed during the follow-up period of seven months.

Conclusion: Timely diagnosis and early surgical intervention play a pivotal role in enhancing the quality of life for individuals with MD. Preoperative medical imaging examinations function as highly effective tools, contributing to heightened surgical safety and a decreased probability of encountering complications during the surgical procedure.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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