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. Author manuscript; available in PMC: 2024 Jan 1.
Published in final edited form as: Clin Endocrinol (Oxf). 2022 Apr 27;98(1):32–40. doi: 10.1111/cen.14743

Table 3:

Comparison between cystic and noncystic pheochromocytoma

Cystic pheochromocytoma Non-cystic Pheochromocytoma*
Median age, years (range) 57 (51–67) 52 (5–84)

Women, (%) 57% 52%

Mode of discovery, %
 Incidental 60% 62%
 Abdominal mass effect 25% -
 Symptoms of hormone excess 10% 26%
 Genetic surveillance 5% 12%

Symptoms of catecholamine excess regardless of the mode of discovery, % 62% 68%

Type of clinical manifestations, %
 Palpitations 62% 56%
 Spells 62% 37%
 Paroxysmal hypertension 54% 40%
 Sustained hypertension 15% -
 Headaches - 43%

Tumor laterality, % Predominantly unilateral Predominantly unilateral, bilateral in 8%

Median tumor size, cm (range) 6.4 (3–19) 4.0 (8–26)

Median unenhanced CT attenuation, HU (range) Cystic component: 18 (13–30) 35 (18–58)
Solid component: 40 (22–50)

Median contrast enhancement, HU (range) Cystic component: 20 (15–33) 83 (22–187)
Solid component: 93 (67–132)

Biochemical profile, %
 Adrenergic 80% 66%
 Noradrenergic 20% 30%
 Nonfunctioning 0% 4%

Median total plasma metanephrines, nmol/L (range) 14.3 (3–223) Median of 2.2–12.4 (0.4–397)#

Median total urinary metanephrines, nmol/L 43000 (10030–494681) Median of 6849–23176 (221–674816)#

Adrenalectomy, %
 Laparoscopic 48% 76%
 Open 52% 24%

Median hospital-stay following surgery, days (range) 4 (1–17) 3 (1–32)

Abbreviations – CT: Computed Tomography, HU: Hounsfield Unit

*

Data from Gruber LM, Hartman RP, Thompson GB, et al. Pheochromocytoma Characteristics and Behavior Differ Depending on Method of Discovery. J Clin Endocrinol Metab. 2019;104(5):1386–1393.

#

Previously reported stratified based on mode of discovery, lowest in patients discovered based on genetic case detection, and highest in patients presenting with symptoms of catecholamine excess. Presented as range of medians.