Objective Routine immunostainings of pituitary adenomas (PAs) have revealed that many are plurihormonal.
Mammosomatotroph adenomas (MSAs), tumors staining for prolactin and growth hormone
(GH), is the most frequent hormone combination. These tumors are derived from a common
progenitor to both mammotrophs and somatotrophs and consequently can have numerous
effects on the endocrine axes. However, these tumors are rare and their presentations,
clinical features, and treatment outcomes are not well understood.
Methods The authors performed a retrospective review over 5 years of PAs resected at our
institution. Data were collected on variables related to clinical presentation, tumor
pathology, radiographic size, and disease recurrence. Tumors were separated into clinical
cohorts and pathological classes. Cohorts were compared with respective non-MSA controls.
Fisher's exact test, ANOVA, student t-test, and the chi-square test were used to measure statistical significance and Bonferroni
corrections were applied as needed.
Results Of 593 PAs, 35 (5.6%) were MSAs staining for GH and prolactin. MSA patients were
younger (49.2/39.9 years, p = 0.001) with comparable gender (49.2%/52.1% female; p = 0.9) as non-MSA patients. MSAs were comparably sized to non-MSAs (1.94/1.90 cm,
p = 0.5). MSAs were divided into four cohorts: (1) 20% had no hormone symptoms; (2)
17% had symptoms of hyperprolactinemia only; (3) 46% had symptoms of acromegaly only;
and (4) 17% had symptoms of both. Cohort 2 MSA patients were more likely to experience
reduced libido (83.3%/7.6%; p = 0.0001) than prolactinomas. Cohort 3 MSA patients were more likely to experience
hyperhidrosis (68.8%/32.6%; p = 0.012) than acromegalics. Two cohort 2 patients were treated with dopamine agonists
for presumed prolactinomas and had biochemical remission without volumetric reduction.
Recurrence rates were comparable in MSAs versus non-MSAs (14%/10%; p = 0.4), and when cohorts were compared with respective controls (p = 0.1–0.3).
Conclusion While silent MSAs presented like hormonally negative adenomas, cohort 2/3 patients
presented with more severe symptoms than prolactinoma/acromegaly patients. MSA must
be considered when evaluating acromegaly or prolactinoma patients, underscoring the
importance of hormone analysis and tumor immunostaining. Even when the second axis
is not elevated, MSA should be suspected in patients who fail medical management.
