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系统性硬化症:一名患者的临床表现、麻醉及骨科相关考量

Systemic sclerosis: Clinical manifestations, anesthetic and orthopedic considerations in a patient.

作者信息

Hasan Obada, Jessar Muneeba, Ashar Muhammad, Noordin Shahryar, Ahmad Tashfeen

机构信息

Orthopedic Surgery Department, The Aga Khan University Hospital, Karachi, Pakistan.

Dermatology Department, Shaheed Mohtarma Benazir Bhutto Medical University, Larkana, Pakistan.

出版信息

Int J Surg Case Rep. 2018;42:24-28. doi: 10.1016/j.ijscr.2017.11.051. Epub 2017 Dec 2.

Abstract

INTRODUCTION

Systemic sclerosis is a rare and progressive multisystem autoimmune disorder that is characterized pathologically by vascular abnormalities, connective tissue sclerosis and atrophy of skin and various internal organs (e.g., alimentary tract, lungs, heart, kidney, CNS), and autoantibodies. With an unknown etiology, Scleroderma is a complex polygenetic disease. A recent Genome Wide Association Study (GWAS) confirmed a strong association with the Major Histocompatibility Complex (MHC) and autoimmunity. We provide a case scenario along with a review of the systems involved and challenges physicians can face in dealing with this rare disease.

CASE PRESENTATION

Our patient, a known case of systemic sclerosis, was admitted with a history of right femur fracture following a fall. We highlight the medical, anesthetic and surgical challenges faced by our team in the management of this patient. We will explain the stages patient faced in treatment process till her death. We combined the case report with detailed literature review of this rare disease.

DISCUSSION

Systemic sclerosis is a complex disease process with many different levels of system involvement. Patient needs to be reviewed thoroughly in preoperative period by multidisciplinary team and counseled in detail about the difficulties in procedure, risks and complications.

CONCLUSION

Patient with scleroderma presents a challenge to the surgical team and anesthetist and a multidisciplinary approach should be followed with all of these patients to avoid catastrophic results.

摘要

引言

系统性硬化症是一种罕见的进行性多系统自身免疫性疾病,其病理特征为血管异常、结缔组织硬化以及皮肤和各种内脏器官(如消化道、肺、心脏、肾脏、中枢神经系统)萎缩,并伴有自身抗体。硬皮病病因不明,是一种复杂的多基因疾病。最近的一项全基因组关联研究(GWAS)证实了其与主要组织相容性复合体(MHC)及自身免疫存在密切关联。我们提供了一个病例,并对所涉及的系统进行了综述,同时阐述了医生在应对这种罕见疾病时可能面临的挑战。

病例介绍

我们的患者是一名已知的系统性硬化症患者,因跌倒后右股骨骨折入院。我们着重介绍了团队在该患者管理过程中所面临的医学、麻醉和手术方面的挑战。我们将解释患者在治疗过程直至死亡所经历的各个阶段。我们将病例报告与对这种罕见疾病的详细文献综述相结合。

讨论

系统性硬化症是一个复杂的疾病过程,涉及多个不同层面系统。术前需要多学科团队对患者进行全面评估,并就手术难度、风险和并发症向患者详细咨询。

结论

硬皮病患者给手术团队和麻醉师带来了挑战,应对所有此类患者采用多学科方法,以避免灾难性后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d1a/5724744/d5fbc2896c87/gr1.jpg

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