ArticleInternal medicine (Tokyo, Japan)2017
Pheochromocytoma Multisystem Crisis Behaving Like Interstitial Pneumonia: An Autopsy Case.
Article in Internal medicine (Tokyo, Japan), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed, 7 citations in OpenAlex.
- Pheochromocytoma Multisystem Crisis Complicated by Severe Acute Pancreatitis.Internal medicine (Tokyo, Japan) · 2023Article
- Clinical characteristics and outcomes of pheochromocytoma crisis: a literature review of 200 cases.Journal of endocrinological investigation · 2022Review
- Diffuse alveolar haemorrhage due to pheochromocytoma crisis.Respirology case reports · 2021Article
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Authors and funding
10 authors at 2 institutions in 1 country.
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Abstract
Pheochromocytoma multisystem crisis is a rare and life-threatening disease that is associated with numerous symptoms and which is also difficult to diagnose. We herein report an autopsy case of a 61-year-old man who died due to pheochromocytoma multisystem crisis. The patient complained of vomiting and breathlessness. Computed tomography showed a shadow-like region with a similar appearance to interstitial pneumonia. The patient was diagnosed with takotsubo cardiomyopathy induced by severe lung disease based on the results of echocardiography and coronary angiography. The patient was treated for interstitial pneumonia. However, his condition rapidly deteriorated and he died 6 hours after arrival. We were later informed of his extremely high catecholamine serum levels. We found pheochromocytoma with hemorrhage at autopsy. The patient's lungs showed acute passive congestion with edema and extravasation.
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