Evidence map›Paper›PMID 41073952›Full record

ReviewBMC pediatrics2025

Takotsubo syndrome as initial presentation of pheochromocytoma in young children: case report and literature review.

Enfu Huang, Ting Zhang, Xiangming Yan, Ling Sun, Yun Zhou

Abstract readCase ReportsReview
In one paragraph

Review in BMC pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Enfu HuangDepartment of Urology, Children's Hospital of Soochow University, Suzhou, Jiangsu, P.R. China.
Ting ZhangDepartment of Urology, Children's Hospital of Soochow University, Suzhou, Jiangsu, P.R. China. zhangting0614@suda.edu.cn.
Xiangming YanDepartment of Urology, Children's Hospital of Soochow University, Suzhou, Jiangsu, P.R. China.
Ling SunDepartment of Cardiology, Children's Hospital of Soochow University, Suzhou, Jiangsu , P.R. China.
Yun ZhouDepartment of Urology, Children's Hospital of Soochow University, Suzhou, Jiangsu, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTakotsubo syndrome is an acute and reversible form of left ventricular dysfunction most often seen in postmenopausal women and typically triggered by extreme emotional or physical stress. Its occurrence in children is exceedingly rare. Pheochromocytoma, a catecholamine-secreting tumor, can mimic Takotsubo syndrome due to its cardiovascular effects. This case is reported for its rarity and to raise awareness of pheochromocytoma as a potentially life-threatening but reversible cause of stress cardiomyopathy in children. CASE PRESENTATION: A 7-year-old boy presented with signs of acute heart failure, including respiratory distress and hypertension. Echocardiography revealed severe left ventricular dysfunction, necessitating invasive mechanical ventilation and high-dose inotropic support. Initial cardiac magnetic resonance imaging and laboratory evaluations were inconclusive. Persistent hemodynamic instability and unexplained cardiac dysfunction prompted a multidisciplinary evaluation. Abdominal magnetic resonance imaging revealed an adrenal mass, and biochemical analysis confirmed elevated catecholamines, leading to a diagnosis of pheochromocytoma. Management included alpha-adrenergic blockade to control hypertension and correct volume status, followed by cautious initiation of beta-blockade. Despite medical therapy, the patient’s cardiac function did not improve significantly, and surgical resection of the adrenal tumor was performed on hospital day 10. Histopathological examination confirmed the diagnosis of pheochromocytoma. Postoperatively, cardiac function improved rapidly.

conclusionsThis case highlights pheochromocytoma as a rare but important differential diagnosis in pediatric patients presenting with acute heart failure and Takotsubo-like cardiomyopathy. Early recognition and targeted management can lead to complete recovery. Increased awareness among pediatricians and cardiologists is essential to avoid delayed diagnosis and improve outcomes in similar cases.

Indexed as

Adrenal Gland NeoplasmsPheochromocytomaTakotsubo CardiomyopathyChildHeart FailureHumansMaleCase reportHeart failurePheochromocytomaTakotsubo syndrome

Identifiers

PMID41073952
PMCPMC12514791

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