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Spontaneous adrenal pheochromocytoma rupture complicated by intraperitoneal hemorrhage and shock
MEN2A is a hereditary syndrome characterized by medullary thyroid carcinoma, hyperparathyroidism, and pheochromocytoma. Classically patients with a pheochromocytoma initially present with the triad of paroxysmal headaches, palpitations, and diaphoresis accompanied by marked hypertension. However, al...
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| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3178469/ https://ncbi.nlm.nih.gov/pubmed/21843357 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1749-7922-6-27 |
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