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Romanian Academy
The Publishing House of the Romanian Academy
ACTA ENDOCRINOLOGICA (BUC)
The International Journal of Romanian Society of Endocrinology / Registered in 1938in Web of Science Master Journal List
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Acta Endocrinologica (Buc)
Erem C, Civan N., Fidan M., Cobanoglu U., Kangül F., Ersoz H.O., Alhan E
Composite Adrenal Pheochromocytoma-Ganglioneuroma in an Adult Patient
Acta Endo (Buc) 2014, 10 (1): 140-149doi: 10.4183/aeb.2014.140
Background. Composite adrenal
pheochromocytoma-ganglioneuromas
(PHEO-GNs) are well-defined neoplasms
of the adrenal medulla, consisting of both
endocrine and neural components. They are
extremely rare. To date, only 46 cases have
been reported in the English literature.
Case report. We describe an
adult case of endocrinologically active
adrenal composite PHEO-GN diagnosed
in a 62-year-old male patient with
history of dizziness, headache, nausea,
vomiting, and uncontrolled hypertension
including intermittant hypertension
attacks. On physical examination, he had
a blood pressure (BP) of 170/110 mmHg.
18-fluorodeoxyglucose positron emission
tomography-computed tomography showed
a right adrenal tumor with increased
metabolic activity. Urinary levels of
catecholamines and their metabolites were
prominently elevated. Right adrenalectomy
was performed for treatment purposes. The
histological diagnosis of the resected tumor
was composite adrenal PHEO-GN.
Conclusions. Composite adrenal
PHEO-GN is a rare entity and preoperative
diagnosis is difficult. Its hormonal activity
and imaging characteristics are frequently
very similar to those of other adrenal tumors,
especially pure PHEO and adrenal carcinoma.
Therefore, careful evaluation by endocrine
tests and multiple imaging procedures are
needed for providing a differential diagnosis.
However, definitive diagnosis composite
adrenal PHEO-GN is established by
histological and immunochemical studies.
To our knowledge, the present case is the
first report that describes composite adrenal
PHEO-GN in a patient from Turkey. We
discuss this case and review the literature on
this unusual entity.
Keywords: Composite adrenal medullar tumor, pheochromocytoma, ganglioneuroma, hypertension.
Correspondence: Cihangir Erem PhD, Medical Faculty, Internal Medicine, KTU Tip Fakultesi, Ic Hastaliklari AbD, Trabzon, 61080, Turkey, E-mail: cihangirerem@hotmail.com