Adrenal Pheochromocytoma—Ganglioneuroma Producing Catecholamines and Various Neuropeptides |
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Authors: | JORMA SALMI,MARKKU PELTO-HUIKKO,OSSI AUVINEN,ANNA-LIISA KARVONEN,JARMO SAARISTO,ILKKA PARONEN,LAURI P
YH
NEN,SEPPO SEPP NEN |
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Affiliation: | JORMA SALMI,MARKKU PELTO-HUIKKO,OSSI AUVINEN,ANNA-LIISA KARVONEN,JARMO SAARISTO,ILKKA PARONEN,LAURI PÖYHÖNEN,SEPPO SEPPÄNEN |
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Abstract: | Abstract. A 65-year-old woman presenting with back pain, difficulties in walking and watery diarrhea. A right adrenal tumor and high excretion of catecholamines were found. Laboratory examinations showed raised levels of vasoactive intestinal polypeptide, pancreatic polypeptide, gastrin and calcitonin. Histology showed a combined pheochromocytoma—ganglioneuroma. The neoplastic cell population was immunohistochemically shown to contain tyrosine hydroxylase, neuropeptide Y, met-enkephalin, substance P, vasoactive intestinal polypeptide, calcitonin and calcitonin gene-related peptide. Postoperatively, the patient recovered fully and the hormone levels returned to normal. |
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Keywords: | pheochromocytoma ganglioneuroma vasoactive intestinal polypeptide pancreatic polypeptide calcitonin gene-related peptide neuropeptide Y enkephalin |
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