Heart myxoma under the mask of interstitial lung lesion: a difficult case from practice

A. V. Novikova, N. Pravdyuk, N. Shostak, N. V. Galimova, D. P. Kotova, D. V. Abeldyaev, G. G. Aleksanyan
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Abstract

The aim of the investigation was to describe a clinical case of the development of interstitial lung lesions in a 57-year-old man with a large left atrial myxoma, which had a reverse development after myxomectomy.Materials and methods. Patient V., 57 years old, was hospitalized in the therapeutic department of the City Clinical Hospital No. 1 named after N. I. Pirogov in connection with bilateral polysegmental pneumonia. A month before hospitalization, he underwent an outpatient examination for progressive dyspnea. Myxoma of the heart was diagnosed. Due to the progression of respiratory failure and the appearance of fever, he was hospitalized. Amidst the multistage antibiotic therapy, there was a torpid course of lung pathology with syndromes of bilateral dissemination and “ground glass”, bilateral lymphadenopathy of the mediastinum, high pulmonary hypertension, and systemic inflammatory reaction syndrome. Thromboembolism of the branches of the pulmonary artery, tuberculosis, sepsis, infective endocarditis, neoplastic processes of pulmonary and other localization were excluded.Results. The clinical picture corresponded to interstitial lung lesions within the framework of paraneoplastic syndrome in heart myxoma. It was decided to urgently carry out myxomectomy.Conclusion. The clinical case demonstrates the development of a rare variant of paraneoplastic syndrome in left atrial myxoma, which was suspected during the patient’s treatment for bilateral polysegmental pneumonia. The progression of the pulmonary lesion was explained by active interstitial inflammation and was supported by the immunological activity of the heart tumor.The performed myxomectomy, despite the persisting syndrome of systemic inflammatory reaction and infiltration of the lung tissue, led in 2 weeks to complete resolution of interstitial lung lesions and pulmonary hypertension, which confirmed the causal relationship between myxoma of the heart and involvement in the pathological process of the lungs.
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肺间质性病变掩盖下的心脏黏液瘤:一例临床疑难病例
本研究的目的是描述一个临床病例间质性肺病变的发展,在一个57岁的男人有一个大的左心房黏液瘤,有一个反向发展的黏液瘤切除术后。材料和方法。患者V., 57岁,因患双侧多节段性肺炎在以n.i.p irogov命名的市第一临床医院治疗科住院。住院前一个月,他接受了进行性呼吸困难门诊检查。确诊为心脏黏液瘤。由于呼吸衰竭的进展和发热的出现,他住院了。在多期抗生素治疗中,肺部病理表现为双侧播散及“磨玻璃”综合征、双侧纵隔淋巴结病、高肺动脉高压、全身性炎症反应综合征。排除肺动脉分支血栓栓塞、肺结核、脓毒症、感染性心内膜炎、肺部肿瘤及其他局限性。临床表现符合心脏黏液瘤副肿瘤综合征框架内的肺间质病变。决定紧急行黏液瘤切除术。本临床病例显示左心房黏液瘤发展为罕见的副肿瘤综合征,在患者治疗双侧多节段性肺炎期间被怀疑。肺病变的进展可以解释为活动性间质炎症,并得到心脏肿瘤免疫活性的支持。行黏液瘤切除术后,尽管全身炎症反应和肺组织浸润综合征持续存在,但2周内肺间质病变和肺动脉高压完全消退,证实了心脏黏液瘤与肺部病理过程受累之间的因果关系。
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