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Histopathological analysis of spontaneous large necrosis of adrenal pheochromocytoma manifested as acute attacks of alternating hypertension and hypotension: a case report

BACKGROUND: Pheochromocytomas are rare catecholamine-producing neuroendocrine tumors. Hypertension secondary to pheochromocytoma is often paroxysmal, and patients occasionally present with sudden attacks of alternating hypertension and hypotension. Spontaneous, extensive necrosis within the tumor th...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:J Med Case Rep
Päätekijät: Ohara, Nobumasa, Uemura, Yasuyuki, Mezaki, Naomi, Kimura, Keita, Kaneko, Masanori, Kuwano, Hirohiko, Ebe, Katsuya, Fujita, Toshio, Komeyama, Takeshi, Usuda, Hiroyuki, Yamazaki, Yuto, Maekawa, Takashi, Sasano, Hironobu, Kaneko, Kenzo, Kamoi, Kyuzi
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2016
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5059976/
https://ncbi.nlm.nih.gov/pubmed/27729064
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-016-1068-3
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