HIGHLIGHTS
- who: J Nepal Med Assoc and colleagues from the Patan Academy of Health Sciences, Satdobato, Lalitpur, Military Hospital Pokhara, Pokhara, Kaski have published the article: JNMA I VOL 61 ISSUE 258 FEBRUARY, in the Journal: (JOURNAL)
- what: The authors report a clinically manifesting giant pheochromocytoma previously being missed because of nonspecific clinical features later landed in pheochromocytoma crisis (PCC).
SUMMARY
Pheochromocytoma (PHEO) and paraganglioma (PGL) are neuroendocrine tumors arising from chromaffin cells of the adrenal medulla and extraadrenal autonomic paraganglioma respectively with a combined estimated annual incidence of 0.8 per . . .
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