Metoclopramide‐Induced Pheochromocytoma Crisis: A Case Report and Literature Review

Pheochromocytoma is a catecholamine-secreting neuroendocrine tumor originating in the adrenal medulla. In patients with pheochromocytoma, paroxysmal over-secretion of catecholamines can be triggered by various medications, including the commonly used antiemetic metoclopramide. We report herein a fatal case of pheochromocytoma crisis triggered by metoclopramide and present a literature review of metoclopramide-induced pheochromocytoma crises to elucidate their clinical characteristics.

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Publication Details

Journal
Clinical Case Reports
Published
2026-02-26
DOI
https://doi.org/10.1002/ccr3.72144
Citations
1
Primary Topic
Adrenal and Paraganglionic Tumors
Type
article
Field-Weighted Citation Impact
39.15
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article

Metoclopramide‐Induced Pheochromocytoma Crisis: A Case Report and Literature Review

Kazuki Iio, Yuki Yamanashi, Wataru Kasahara, Keiki Shimizu et al.
1 citations
Clinical Case Reports
Adrenal and Paraganglionic Tumors
39.15
article

Metoclopramide‐Induced Pheochromocytoma Crisis: A Case Report and Literature Review

Kazuki Iio, Yuki Yamanashi, Wataru Kasahara, Keiki Shimizu, Jun Hamaguchi
article en
1 citations

Abstract

Pheochromocytoma is a catecholamine-secreting neuroendocrine tumor originating in the adrenal medulla. In patients with pheochromocytoma, paroxysmal over-secretion of catecholamines can be triggered by various medications, including the commonly used antiemetic metoclopramide. We report herein a fatal case of pheochromocytoma crisis triggered by metoclopramide and present a literature review of metoclopramide-induced pheochromocytoma crises to elucidate their clinical characteristics.

Clinical Case ReportsVol. 14(3)
Tokyo Metropolitan Children's Medical Center (JP), Tokyo Metropolitan Tama Medical Center (JP)
Zero hunger
Openalex Percentile: Top 0%
Adrenal and Paraganglionic Tumors
39.15
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