Evidence map›Paper›PMID 41181484›Full record

ArticleAnnals of medicine and surgery (2012)2025

Takayasu arteritis presenting with severe biventricular dysfunction and renal artery stenosis in a pediatric patient: a case report.

Kundan Kumar Yadav, Srijana Kumari Yadav, Suraj Pariyar, Asim Shrestha, Vivek Karn, Sunita Tamang, Punam Adhikari, Rajni Karki, Ravi Kumar Yadav

Abstract readCase Reports
In one paragraph

Article in Annals of medicine and surgery (2012), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

9 authors.

Kundan Kumar YadavMaharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal.
Srijana Kumari YadavMaharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal.
Suraj PariyarMaharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal.ORCID https://orcid.org/0009-0002-9350-3370
Asim ShresthaMaharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal.ORCID https://orcid.org/0009-0009-6428-4026
Vivek KarnDepartment of Pediatrics, Maharajgunj Medical Campus, Tribhuvan University Teaching Hospital, Nepal.
Sunita TamangDepartment of Pediatrics, Maharajgunj Medical Campus, Tribhuvan University Teaching Hospital, Nepal.
Punam AdhikariDepartment of Pediatrics, Maharajgunj Medical Campus, Tribhuvan University Teaching Hospital, Nepal.
Rajni KarkiDepartment of Pediatrics, Maharajgunj Medical Campus, Tribhuvan University Teaching Hospital, Nepal.
Ravi Kumar YadavUniversal College of Medical Sciences, Ranigaun, Bhairahawa, Nepal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction and importance: Takayasu arteritis (TA), a rare chronic granulomatous vasculitis, predominantly affects large- and medium-sized arteries, such as the aorta and its branches. It can lead to life-threatening complications, particularly in pediatric cases where delayed diagnosis and multi-organ involvement are common. Systemic hypertension and vascular abnormalities, including renal artery stenosis, are significant manifestations that pose diagnostic and therapeutic challenges. Case presentation: We report the case of a 14-year-old girl from Nepal who presented with severe biventricular dysfunction, refractory systemic hypertension, and generalized anasarca. Initial investigations revealed bilateral renal artery stenosis and circumferential wall thickening of the abdominal aorta, confirming a diagnosis of TA. Despite aggressive medical management with immunosuppressive therapy and antihypertensives, her condition remained critical, necessitating urgent percutaneous transluminal renal artery angioplasty. The angioplasty successfully restored renal artery perfusion, resulting in significant clinical improvement and normalization of blood pressure. Her cardiac function stabilized, and she was discharged on a reduced antihypertensive regimen. Follow-up imaging demonstrated sustained renal artery patency. Clinical discussion: This case underscores the importance of early diagnosis, multidisciplinary management, and timely interventional procedures in pediatric TA. Renal artery stenosis in TA can exacerbate hypertension and cardiac dysfunction, as seen in this patient. The success of angioplasty highlights the potential of interventional radiology as a life-saving modality in severe cases. Conclusion: Pediatric TA with multi-organ involvement requires a coordinated, multidisciplinary approach for optimal outcomes. This case exemplifies the complexities of managing refractory hypertension and advanced vascular complications in TA and emphasizes the critical role of advanced interventional techniques.

Indexed as

biventricular dysfunctionhypertensionpediatric vasculitisrenal artery stenosisTakayasu arteritis

Identifiers

PMID41181484
PMCPMC12577941

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