Evidence map›Paper›PMID 41959984›Full record

ArticleCureus2026

Catecholamine-Induced Multiorgan Failure and Arterial Thrombosis: A Rare Manifestation of Pheochromocytoma in the Setting of Community-Acquired Pneumonia.

Ahd Elmahi, Maitha Humaid Ibrahim, Rehab Mohd Jamali, Tahsina Tajnin Sadia, Mohamed Ragab Radwan

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In one paragraph

Article in Cureus, 2026. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ahd ElmahiCollege of Medicine, University of Sharjah, Sharjah, ARE.
Maitha Humaid IbrahimCollege of Medicine, University of Sharjah, Sharjah, ARE.
Rehab Mohd JamaliCollege of Medicine, University of Sharjah, Sharjah, ARE.
Tahsina Tajnin SadiaCollege of Medicine, University of Sharjah, Sharjah, ARE.
Mohamed Ragab RadwanDepartment of Emergency Medicine, Al Qassimi Hospital, Sharjah, ARE.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pheochromocytoma is a rare catecholamine-secreting tumor that has a highly variable presentation and may result in life-threatening complications. In the most severe cases, massive release of catecholamines can lead to refractory shock, acute cardiomyopathy, and multiorgan failure. The diverse clinical manifestations of pheochromocytoma often make diagnosis challenging in critical care settings. We report a 25-year-old woman who presented with acute abdominal pain, vomiting, pleuritic chest pain, and a productive cough and was initially managed as community-acquired pneumonia complicated by septic shock. She rapidly deteriorated, requiring intubation, vasopressor support, and advanced cardiac life support following cardiac arrest. Bedside echocardiography showed severe global left ventricular systolic dysfunction with an estimated ejection fraction of 20%-25%. During her stay in the intensive care unit, a femoral catheterization was performed for vascular access and hemodynamic monitoring. However, in the context of a catecholamine excess state, she subsequently developed acute ischemia of the left lower limb. Computed tomography angiography (CTA) showed extensive arterial occlusion, and an incidental 4 × 4 cm left adrenal mass was discovered. Follow-up biochemical testing showed markedly elevated plasma metanephrines and normetanephrines, supporting the diagnosis of pheochromocytoma. Despite treatment with thrombectomy, her limb ischemia was irreversible, necessitating an above-knee amputation. With supportive care and initiation of α-adrenergic and β-adrenergic blockade, her cardiac and renal function gradually improved. She was stabilized and referred for definitive surgical management. This case highlights that pheochromocytoma crisis may mimic septic shock and can present with severe cardiomyopathy and limb-threatening arterial thrombosis. Early consideration of catecholamine excess in unexplained refractory shock or multiorgan failure is important, since early diagnosis and targeted treatment can be lifesaving and help prevent irreversible complications.

Indexed as

arterial thrombosiscardiomyopathymulti-organ failurepheochromocytomaseptic shock

Identifiers

PMID41959984
PMCPMC13061532

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