Pheochromocytoma Diagnosed during the Treatment of Diffuse Alveolar Hemorrhage, a Diagnostic Necessity before Using High-dose Glucocorticoids

A 46-year-old woman with exacerbating hemoptysis and dyspnea was diagnosed with diffuse alveolar hemorrhage (DAH). High doses of glucocorticoids were initiated, but afterward, paroxysmal hypertension (210/140 mmHg) with headache and abdominal pain appeared. A 50-mm left adrenal tumor with an intense...

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Published inInternal Medicine Vol. 60; no. 17; pp. 2825 - 2830
Main Authors Nezu, Masahiro, Kobayashi, Hiroaki, Shiozaki, Masashi, Katsumata, Miho, Takizawa, Soichi, Tsutsui, Toshiharu, Nukui, Ikuo, Miyashita, Yoshihiro, Oyama, Toshio, Inoue, Masaharu
Format Journal Article
LanguageEnglish
Published Japan The Japanese Society of Internal Medicine 01.09.2021
Japan Science and Technology Agency
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Summary:A 46-year-old woman with exacerbating hemoptysis and dyspnea was diagnosed with diffuse alveolar hemorrhage (DAH). High doses of glucocorticoids were initiated, but afterward, paroxysmal hypertension (210/140 mmHg) with headache and abdominal pain appeared. A 50-mm left adrenal tumor with an intense uptake by iodine-123 metaiodobenzylguanidine scintigraphy and catecholamine hypersecretion revealed complication with pheochromocytoma. Because high doses of glucocorticoids, sometimes required for DAH, can provoke life-threatening paroxysmal hypertension in pheochromocytoma and paraganglioma (PPGL), our case suggests that PPGL needs to be recognized as the cause of DAH and should be detected with whole-body imaging before starting glucocorticoids.
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Correspondence to Dr. Masahiro Nezu, nezumasahiro@med.tohoku.ac.jp
ISSN:0918-2918
1349-7235
DOI:10.2169/internalmedicine.6827-20