Rare clinical case of the diagnosis of idiopathic pulmonary artery hypertension

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In this work, a rather rare (morbidity of about 1–2 cases per 1 million of adult population per year) and interesting clinical case of the diagnosis of idiopathic pulmonary artery hypertension (IPAH) was described. This case was also known as Ayerza disease or Ayerza–Arilago syndrome. At the initial stage, this pathology was characterized by an asymptomatic course that caused certain difficulties in making a correct diagnosis. In general, this disease had a poor prognosis. The main cause of death was decompensated right ventricular failure. The occurrence of complications could be significantly reduced and the life quality of such patients could be improved by the timely diagnosis and correct approach.

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作者简介

Grigory Ignatenko

M. Gorky Donetsk National Medical University

Email: gai-1959@mail.ru
ORCID iD: 0000-0002-1155-563X

MD, Dr.Sci.(Med.), Professor, Corresponding Member of the Ukraine National Academy of Medical Sciences, Honored Scientist and Technician of Ukraine, Rector, Head of the Propaedeutic and Internal Medicine Department

乌克兰, Donetsk

Ilya Grekov

M. Gorky Donetsk National Medical University

Email: ilya.grekov.1998@gmail.com
ORCID iD: 0000-0002-6140-5760

6th year student

乌克兰, Donetsk

Marina Grushina

M. Gorky Donetsk National Medical University

编辑信件的主要联系方式.
Email: grushinamarina@inbox.ru
ORCID iD: 0000-0003-3670-3376

MD, Cand.Sci.(Med.), , Associate Professor of the Propaedeutic and Internal Medicine Department

乌克兰, Donetsk

Anna Dubovyk

M. Gorky Donetsk National Medical University

Email: dubovyk-anna@mail.ru
ORCID iD: 0000-0002-8753-3824

MD, Cand.Sci.(Med.), , Associate Professor of the Propaedeutic and Internal Medicine Department

乌克兰, Donetsk

参考

  1. Chazova IE, Martynyuk TV, Valieva ZS, et al. Eurasian clinical guidelines on diagnosis and treatment of pulmonary hypertension. Eurasian Heart Journal. 2020;(1):78-122. (In Russ.) doi: 10.38109/2225-1685-2020-1-78-122
  2. Galiè N, Humbert M, Vachiery J-L, et al. 2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension. European Respiratory Journal. 2015;46(4):903-75. doi: 10.1183/13993003.01032-2015
  3. Kochetov VE. Aerza-Arrilaga syndrome: pathogenesis and pathophysiology. Bulletin of Emergency Medicine. 2016; 9(1):107-11. (In Russ).
  4. Tsareva NA. Updated classification and diagnosis of pulmonary hypertension. Consilium Medicum. 2017;19(3):66-71. (In Russ).
  5. Martyniuk TV, Chazova IE. Strategy of medical treatment of pulmonary arterial hypertension in the current international recommendations. Systemic Hypertension. 2016;13(2):46-64. (In Russ).

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版权所有 © Ignatenko G., Grekov I., Grushina M., Dubovyk A., 2021


Media Registry Entry of the Federal Service for Supervision of Communications, Information Technology and Mass Communications (Roskomnadzor) PI No. FS77-76803 dated September 24, 2019.



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