Case report Takayasu arteritis in a rural hospital in Indonesia

Michael Lusida, Michael and Mohammad Zakky Kurniawan, Mohammad and Johanes Nugroho Eko Putranto, Johanes Case report Takayasu arteritis in a rural hospital in Indonesia. BMJ Case Reports, 13 (1). ISSN 1757-790X

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Official URL: https://casereports.bmj.com/content/13/1/e230884

Abstract

Abstract Takayasu arteritis (TA) is a rare chronic granulomatous inflammation of the aorta or its branches and is prevalent all around the world. It causes stenosis of large arteries and ischaemic damage to target organs. There is usually a delay in recognising TA because of the rarity and unfamiliarity with the disease, unspecific early symptoms and lack of diagnostic equipment for early diagnosis. In this report, we present a case of an 18-year-old woman from Pasuruan, East Java, Indonesia, with recurrent fever, headache, claudication of extremities and postprandial abdominal pain. She was diagnosed clinically with suspicion of TA and was sent to a tertiary hospital to confirm the diagnosis. Arteriography revealed that the patient had narrowing of the thoracic and abdominal aorta until the level of the aortic bifurcation. The patient was started on high-dose corticosteroid, cyclosporine A and diltiazem. The patient then showed improvement in her symptoms.

Item Type: Article
Subjects: R Medicine > R Medicine (General) > R5-920 Medicine (General)
Divisions: 01. Fakultas Kedokteran > Ilmu Kardiologi Dan Kedokteran Vaskular (Spesialis)
Creators:
CreatorsNIM
Michael Lusida, MichaelUNSPECIFIED
Mohammad Zakky Kurniawan, MohammadUNSPECIFIED
Johanes Nugroho Eko Putranto, JohanesNIDK: 8866900016
Depositing User: arys fk
Date Deposited: 25 Feb 2023 06:36
Last Modified: 25 Feb 2023 06:36
URI: http://repository.unair.ac.id/id/eprint/120129
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