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  • Alveolar proteinosis as a rare case of in the practice of a pulmonologist

    Редактор | 2018, Clinical case, Practical medicine part 16 №7 (part 2) Innovative technologies in medicine (2018) | 31 октября, 2018

    V.I. ILINSKIY2, N.G. SHAMSUTDINOVA1, G.I. NURULLINA1, L.I. MINGAZOVA2, V.O. MITRIKOVA1, A.A. SAYFEEVA1

    1Kazan State Medical University of the MH of RF, 49 Butlerov Str., Kazan, Russian Federation, 420012

    2Republican Clinical Hospital of the Ministry of Healthcare of the Republic of Tatarstan, 138 Orenburgskiy trakt, Kazan, Russian Federation, 420064

     Ilinskiy V.I. ― Head of the Pulmonology Department, tel. (843) 237-36-26, e-mail: Victor.Ilinskiy@tatar.ru

    Shamsutdinova N.G. ― D. Sc. (medicine), Assistant of the Department of Hospital Therapy, e-mail: nailya@e-diva.ru

    Nurullina G.I. ― Assistant of the Pulmonology Department, e-mail: nurguzel@mail.ru, ORCID ID: 0000-0002-7697-187X

    Mingazova L.I. ― Doctor of the Pulmonology Department, tel. (843) 237-36-26, e-mail: Victor.Ilinskiy@tatar.ru

    Mitrikova V.O. ― the 4th year student of the Faculty of Medicine, e-mail: v.mitrikova@mail.ru, ORCID ID:  0000-0002-5392-6144

    Saifeeva A.A. ― the 4th year student of the Faculty of Medicine, e-mail: m172463@mail.ru, ORCID ID:  0000-0002-6335-4733

    The article presents information about the disease «alveolar proteinosis», its forms, clinical manifestations and prognosis are considered. The issues of etiology, pathogenesis and diagnosis of pulmonary alveolar proteinosis (PAP) are outlined. To diagnose the described unique clinical case, modern diagnostic methods were applied. After confirming the diagnosis, the patient underwent high-volume therapeutic bronchoalveolar lavage of both lungs. As a result of the treatment, a significant improvement in the patient’s condition was achieved, which indicates the effectiveness of the treatment.

    Key words: alveolar proteinosis, clinical forms, prognosis, respiratory failure.

     (For citation: Ilinskiy V.I., Shamsutdinova N.G., Nurullina G.I., Mingazova L.I., Mitrikova V.O., Saifeeva A.A. Alveolar proteinosis as a rare case of in the practice of a pulmonologist. Practical Medicine. 2018)

     REFERENCES

    1. Kitamura T., Tanaka N., Watanabe J. et al. Idiopathic pulmonary alveolar proteinosis as an autoimmune disease with neutralizing antibody against granulocyte/macrophage colony-stimulating factor. J. Exp. Med, 1999, 190, pp. 875-80.
    2. Trapnell B.C., Whitsett J.A., Nakata K. Pulmonary alveolar proteinosis. N. Engl. J. Med, 2003, 349, pp. 2527-2539. doi: 10.1056/NEJMra023226.
    3. Ceruti M., Rodi G., Stella G.M. et al. Successful whole lung lavage in pulmonary alveolar proteinosis secondary to lysinuric protein intolerance: a case report. Orphanet Journal of Rare Diseases, 2007, pp. 1750-7.
    4. Xie L., Zhao T., Wang Q. et al. Secondary pulmonary alveolar proteinosis associated with myelodisplastic syndrome. Clin. Med. J, 2007, 120 (12), pp. 1114-6.
    5. Ishii H., Trapnell B.C., Tazawa R. et al. Comparative study of high-resolution CT findings between autoimmune and secondary pulmonary alveolar proteinosis. Chest, 2009, 136, pp. 1348-1355. doi: 10.1378/chest.09-0097.

    Метки: 2018, A.A. SAYFEEVA, alveolar proteinosis, clinical forms, G.I. NURULLINA, L.I. MINGAZOVA, N.G. SHAMSUTDINOVA, Practical medicine part 16 №7 (part 2) Innovative technologies in medicine (2018), prognosis, respiratory failure, V.I. ILINSKIY, V.O. MITRIKOVA

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