Diagnosis

Interactive Quiz: Galactorrhea and Elevated Prolactin Levels

what's your diagnosis?

 

Welcome to Consultant360's latest interactive diagnostic quiz. Over the next few pages, we'll present a case and ask you to make the diagnosis and treat the patient. Along the way, we'll provide details about the case, and at the end, we'll share the patient’s outcome.

Ready to get started?

First, let’s meet the patient.

 

A 34-year-old woman presented with a history of bilateral galactorrhea for the past 4 years. She also reported having amenorrhea and chronic low-grade persistent headache. She denied a history of medication use or substance abuse. She had no known food or drug allergies. Her medical history was not significant.

 

At presentation, the patient’s blood pressure was 130/80 mm Hg, pulse was 75 beats/min, and respiratory rate was 16 breaths/min. Her height was 160 cm and weight was 71.2 kg, corresponding to a body mass index of 27.8 kg/m2. The patient was alert, orientated, and in no acute distress. Visual acuity was 20/20 in both eyes, and temporal homonymous hemianopia was present. There was no iritis or iridocyclitis. Neurological examination findings were benign. Examination of the breasts showed that the nipples were not retracted, although a brownish white discharge was noted; no areolar skin abnormities were detected. No lumps were noted in either breast. Thyroid examination findings were normal.

 

Laboratory test results included a grossly elevated serum prolactin level of 180.6 µg/L (reference range, 2-29 µg/L), a normal chorionic gonadotropin level below 1 mIU/mL (reference range, <5 mIU/mL), a normal follicle-stimulating hormone level of 7.5 mIU/mL (reference range, 2.5-10.2 mIU/mL), and a normal luteinizing hormone level of 8.2 mIU/mL (reference range, 2.4-12.6 mIU/mL). All other test results, including thyroid function, sodium, calcium, glucose, cholesterol, hemoglobin, albumin, creatinine, and urea nitrogen values, were within normal reference ranges. Magnetic resonance imaging of the pituitary showed a cystic nodule measuring 6.5 × 6.2 mm in the left posterolateral aspect (Figure).

See the patient’s MRI

pituitary nodule

Figure: Sellar MRI (coronal view) showing the partially cystic prolactinoma on T2-weighted image

 

What’s your diagnosis?

 

Is Your Answer Correct?

Answer: Microprolactinoma

 

Based on the clinical presentation and diagnostic test results, the patient received a diagnosis of microprolactinoma.

 

Prevalence of prolactinomas

 

Find out!

Answer: Younger women

 

A prolactinoma is a tumor of lactotrophs and is the most common (40%-57%) of the benign and secretory adenomas. Classified based on size, microadenomas are less than 10 mm while macroadenomas are 10 mm or larger. Another classification system is based on the type of cells from which the prolactinoma originates and the hormone secreted.1,2 Furthermore, prolactinomas (mostly microadenomas) are prevalent among women (78%-81%), mainly affecting younger females.3,4 The exact etiology is still being explored; nonetheless, mutations in several genes have been noted in association with sporadic and hereditary cases of prolactinomas.5,6

 

Clinical symptoms of prolactinomas originate from mass effect (tumor growth) and hormone hypersecretion. Specifically, hyperprolactinemia in women can cause menstrual irregularities, galactorrhea, and visual field defects,6 as in the case of our patient. The treatment of patients with microprolactinomas expressing hyperprolactinemia should address the issue of tumor growth and alleviate the associated mass effect, as well as restore normal hormone levels.7,8

 

How are prolactinomas most commonly treated?

 

See the answer!

Answer: Medication

 

Prolactinomas are primarily treated with dopamine agonists, bromocriptine, cabergoline, pergolide, quinagolide, lisuride, and terguride, as well as a serotonin antagonist, metergoline.8,9 Surgery and radiotherapy are also options in cases of patients with expanding prolactinomas, who are not responding well to pharmacotherapy, or with a worsening of vision.9 Most patients respond well to treatment with dopamine agonists, and visual defects disappear; however, visual field testing can be done in some instances.10,11 Several other classes of experimental drugs are being evaluated, including somatostatin analogues, selective estrogen-receptor modulators, prolactin-receptor antagonists, temozolomide, and gene therapy.12,13

 

Outcome of the case

Outcome of the Case

 

Our patient is responding well to bromocriptine pharmacotherapy and is being evaluated on regular basis. 

 

 

Authors:


Syed A. A. Rizvi, PhD, MS, MBA; and Jasmin Ahmed, MD
Larkin Community Hospital, South Miami, Florida

 

Sultan S. Ahmed, MD
Nova Southeastern University, Fort Lauderdale, Florida

 

Ayman M. Saleh, PhD
King Saud bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia

 

Nada A. Saleh, MBBS
University of Jordan, Amman, Jordan

 

 

Citation: 
Rizvi SAA, Ahmed SS, Saleh AM, Saleh NA. Microprolactinoma. Consultant. 2018;58(8):219-220. 

 

 

References:

 

  1. Klibanski A. Prolactinomas. N Engl J Med. 2010;362(13):1219-1226.
  2. Lake MG, Krook LS, Cruz SV. Pituitary adenomas: an overview. Am Fam Physician. 2013;88(5):319-327.
  3. Colao A, Di Sarno A, Cappabianca P, et al. Gender differences in the prevalence, clinical features and response to cabergoline in hyperprolactinemia. Eur J Endocrinol. 2003;148(3):325-331.
  4. Day PF, Loto MG, Glerean M, Picasso MFR, Lovazzano S, Giunta DH. Incidence and prevalence of clinically relevant pituitary adenomas: retrospective cohort study in a health management organization in Buenos Aires, Argentina. Arch Endocrinol Metab. 2016;60(6):554-561.
  5. Phillips J, East HE, French SE, et al. What causes a prolactinoma to be aggressive or to become a pituitary carcinoma? Hormones (Athens). 2012;11(4):477-482.
  6. Rogers A, Karavitaki N, Wass JAH. Diagnosis and management of prolactinomas and non-functioning pituitary adenomas. BMJ. 2014;349:g5390.
  7. Ali S, Miller KK, Freudenreich O. Management of psychosis associated with a prolactinoma: case report and review of the literature. Psychosomatics. 2010;51(5):370-376.
  8. Gillam MP, Molitch ME, Lombardi G, Colao A. Advances in the treatment of prolactinomas. Endocr Rev. 2006;27(5):485-534.
  9. Molitch ME. Endocrinology in pregnancy: management of the pregnant patient with a prolactinoma. Eur J Endocrinol. 2015;172(5):R205-R213.
  10. Woodhouse NJY, Khouqueer F, Sieck JO. Prolactinomas and optic nerve compression: disappearance of suprasellar extension and visual recovery after two weeks bromocriptine treatment. Horm Res. 1981;14(3):141-147.
  11. Almalki MH, Alzahrani S, Alshahrani F, et al. Managing prolactinomas during pregnancy. Front Endocrinol (Lausanne). 2015;6:85.
  12. dos Santos Nunes V, El Dib R, Boguszewski CL, Nogueira CR. Cabergoline versus bromocriptine in the treatment of hyperprolactinemia: a systematic review of randomized controlled trials and meta-analysis. Pituitary. 2011;​14(3):259-265.
  13. Colao A, Savastano S. Medical treatment of prolactinomas. Nat Rev Endocrinol. 2011;7(5):267-278.