THE COMBINATION OF PULMONARY ALVEOLAR MICROLITHIASIS AND PNEUMOCONIOSIS – A CLINICAL CASE

L.A. Shpagina, I.S. Shpagin, O.S. Kotova, S.A. Karmanovskaya, L.A. Panacheva, I.P. Mikhno, E.G. Konduyrina, V.V. Zelenskaya, E.M. Loktin
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Abstract

Pulmonary alveolar microlithiasis is a rare genetic disease characterized by the formation of intraalveolar calcium phosphate microliths. Clinical and radiological manifestations are similar to pneumoconiosis, which makes it difficult to diagnose a comorbid condition. This article presents a case from clinical practice: a 30-year-old male patient, non-smoker was referred to a occupational pathology center with a preliminary diagnosis of pneumoconiosis. He worked for 8 years under conditions of exposure to highly fibrogenic dust with the maximum allowable concentrations in the air of the working area exceeding by 2.3–2.1 times. During this period, preliminary and 3 periodic medical examinations were carried out which did not reveal any contraindications for continuing work. Examination at the center of occupational pathologists revealed signs of respiratory failure of the 2nd degree, severe pulmonary hypertension and radiological diffuse dissemination syndrome with small shading of two types - a large number of high (calcium) density foci with clear edges and a moderate number of medium density foci. Histological examination revealed signs of pulmonary fibrosis and interstitial inflammation of the type of nonspecific interstitial pneumonia, microliths located intraalveolarly, as well as a small amount of granulomas with hyalinosis in the center, a concentric arrangement of collagen fibers, fibroblasts, alveolar macrophages. A comorbid disease was diagnosed – pulmonary alveolar microlithiasis in combination with pneumoconiosis confirmed by the results of genetic testing – the c.1328delT mutation of the SLC34A2 gene was detected. The further course of the disease was characterized by progression of dyspnea and desaturation, an increase in the number of high-density foci in the lungs. 2 years after diagnosis – death due to respiratory failure. The presented case demonstrates the possibility of a combination of pulmonary alveolar microlithiasis with pneumoconiosis and an unfavorable prognosis of a comorbid disease.
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肺泡微石症合并尘肺病1例
肺泡微石症是一种罕见的遗传性疾病,其特征是肺泡内形成磷酸钙微石。临床和放射学表现与尘肺相似,因此很难诊断合并症。本文报告一例临床病例:一位30岁男性患者,不吸烟,被转介到职业病理中心,初步诊断为尘肺病。他在高纤维性粉尘暴露条件下工作了8年,工作区域空气中最大允许浓度超过2.3-2.1倍。在此期间,进行了初步和3次定期体检,没有发现任何继续工作的禁忌。在职业病理学中心检查发现二级呼吸衰竭、严重肺动脉高压和影像学弥漫性播散综合征,伴有两种类型的小阴影-大量高(钙)密度病灶,边缘清晰,中等数量的中密度病灶。组织学检查示肺纤维化和非特异性间质性肺炎间质性炎症征象,肺泡内可见小结石,中心可见少量肉芽肿伴透明质变性,胶原纤维、成纤维细胞、肺泡巨噬细胞呈同心排列。诊断为合并症-肺泡微石症合并尘肺病,基因检测结果证实-检测到SLC34A2基因的c.1328delT突变。该疾病的进一步病程以呼吸困难和去饱和进展为特征,肺部高密度灶的数量增加。诊断后2年-因呼吸衰竭死亡。本病例显示肺泡微石症合并尘肺病的可能性及合并症的不良预后。
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