SINDROME ANTISINTETASA EN TIEMPO DE PANDEMIA

Eddyn Ruben Macías, Carlos Luis Aguilar, Andrés Vinicio Cuenca
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Abstract

Introduction Introduction: The Antisynthetase Syndrome is a rare entity that is included within the idiopathic inflammatory myopathies, characterized by the presence of antisynthetase antibodies, they can be found in 39.1% of the patients with these myopathies. The affectation is systemic being the main ones at the articular level in 40% -80%. Lung damage occurs in 60% -80%, the most frequent findings being ground glass, predominantly crosslinking in lower segments, probably with a pattern of non-specific interstitial pneumonia, organized pneumonia, or mixed patterns. Regarding muscle involvement, it occurs in 60% -80%. Treatment is based on the use of corticosteroids, immunosuppressants, and biological agents. Case description A 38-year-old female patient with no significant clinical or family history was approached, single (no children), who presented gradual and intermittent joint pain and muscle weakness associated with progressive dyspnea, in the context of The current pandemic was swabbed for SARS-COV-2 on two occasions as well as antibodies for the same virus being negative, with tomographic findings compatible with an alternative pattern, despite the aforementioned, it was treated in a particular way with a scheme directed towards COVID -19, with partial resolution of the symptoms and subsequent exacerbation of the same, for which he went to hospital care, where the swab was repeated obtaining negativity of the same, deciding on this occasion an evaluation by the Pneumology Service and hospitalization. During his stay, an immunological panel was performed where a weak elevation of rheumatoid factor is evidenced, due to logistical issues Myositis panel we are waiting, however, due to the lack of specific etiology, it was decided to perform a lung biopsy reporting a concordant pattern of organized pneumonia With the tomographic diagnosis, the evolution of the patient was favorable with supportive treatment until the results of the external immunological panel were received, evidencing a marked elevation of the anti-Jo antibody, added to the clinical and image manifestations, the picture is cataloged as an Antisynthetase Syndrome. Thus, with the support of rheumatology, treatment with corticosteroids (methylprednisolone), immunosuppressants (mycophenolate) and biological agent (rituximab) is started; with which there was significant clinical improvement, decrease in o2 support as well as lung lesions, with which we proceeded to discharge with the respective follow-up by the services involved. Conclusions: As we evidenced in the clinical case, in a retrospective way, we can assert that it complied with the clinical manifestations of the disease, although we are experiencing a pandemic where lung involvement is important, once it has been ruled out, other diagnostic possibilities must be addressed. As in the patient, it culminated in the presentation of a rheumatological picture with lung damage.
大流行时期的抗合成酶综合征
抗合成酶综合征是一种罕见的特发性炎性肌病,以存在抗合成酶抗体为特征,39.1%的肌病患者存在抗合成酶抗体。40% -80%的患者在关节水平以全身性为主。肺损伤发生率为60% -80%,最常见的表现为磨砂玻璃,主要是下节段交联,可能伴有非特异性间质性肺炎、组织性肺炎或混合型。关于肌肉受累,发生率为60% -80%。治疗的基础是使用皮质类固醇、免疫抑制剂和生物制剂。病例描述接触了一名38岁女性患者,无明显临床或家族史,单身(无子女),在当前大流行的背景下,出现渐进式和间歇性关节疼痛和肌肉无力,两次拭子检测SARS-COV-2,同一病毒的抗体为阴性,断层扫描结果与另一种模式相符,尽管上述情况。根据针对COVID -19的特定方案对其进行了治疗,症状得到部分缓解,随后病情加重,为此他去了医院护理,在那里反复使用拭子获得相同的阴性结果,并决定在此情况下由肺炎科进行评估并住院治疗。在他住院期间,在类风湿因子轻度升高的情况下进行了免疫检查,由于后勤问题,我们正在等待肌炎检查,然而,由于缺乏具体的病因,我们决定进行肺活检,报告有组织肺炎的一致模式。随着断层扫描诊断,在收到外部免疫检查结果之前,患者的发展有利于支持性治疗。由于抗jo抗体明显升高,加上临床和图像表现,该图被归类为抗合成酶综合征。因此,在风湿病学的支持下,开始使用皮质类固醇(甲基强的松龙)、免疫抑制剂(霉酚酸酯)和生物制剂(利妥昔单抗)进行治疗;有了显著的临床改善,氧气支持减少以及肺部病变,我们继续出院,由相关服务部门进行相应的随访。结论:正如我们在临床病例中所证明的那样,通过回顾性分析,我们可以断言,它符合该疾病的临床表现,尽管我们正在经历一场大流行,肺部受累很重要,但一旦排除了它,就必须考虑其他诊断可能性。与本例患者一样,最终表现为风湿病学图像伴肺损伤。
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