Description
A 68-year-old man presented with a 5-day history of left-sided hemiparesis, dysphasia and abnormal gait.
His medical history included type 2 diabetes mellitus, hypertension and previous craniopharyngioma, treated with complex surgical debulking and subsequent radiotherapy 13 years earlier. As a result, the patient developed panhypopituitarism (gonadotrophin deficiency, growth hormone deficiency, adrenocorticotropic deficiency, thyrotropin deficiency and diabetes insipidus) and remained under the care of the endocrine team.
His treatment included replacement testosterone, growth hormone, hydrocortisone, levothyroxine, desmopressin and metformin for type 2 diabetes mellitus.
Clinical examination revealed left-sided hemiplegia with upper-motor-neurone signs and global dysphasia. Blood profile was normal. Given his history, it was initially felt this presentation was linked to his previous intracranial disease. However, an urgent CT of the head scan revealed an area of low attenuation in the right pons (figure 1). This was confirmed to be a right hemipontine infarct on MRI of the brain (figures 2 and 3).
The patient was admitted to the stroke unit and started on antiplatelet and secondary prevention medications. Thrombolysis was not considered as he presented well over 4.5 hours from onset of symptoms. Following prolonged neurorehabilitation, he regained most of his motor function and was discharged home.
Radiotherapy treatment for craniopharyngioma has been shown to increase cerebrovascular disease risk and mortality rate.1 The mechanisms proposed are direct radiation damage to cerebral vasculature and pituitary hormone deficiency.1 Hypopituitarism occurs in 50% of patients after a decade and the incidence increases with time from treatment.1 Interestingly, hypopituitarism occurs sooner if a higher dose of radiotherapy is used.1
Learning points.
Craniopharyngiomas are benign suprasellar tumours derived from embryonic pituitary tissue.2 Although benign in nature and slow-growing, complications arise due to mass effect on adjacent structures, and patients often present with headache, bitemporal hemianopia and symptoms of hypopituitarism.2 Patients with craniopharyngiomas should be managed by a multidisciplinary team and require long-term endocrinology input.2 3
Review of the literature suggests postoperative treatment with radiotherapy of craniopharyngioma increases the long-term risk of stroke later in life.1 In our patient, there were added cardiovascular risks with existing hypertension and type 2 diabetes.
Occam's razor is a useful tool in clinical medicine, to formulate a unifying medical diagnosis but, as shown in this case, sometimes patients can have the double jeopardy of presenting with two different medical diagnoses. Clinicians should exercise good clinical acumen and keep an open mind to ensure they are not missing a significant diagnosis.
Footnotes
Contributors: ISB consented the patient, provided the title, reviewed the literature and wrote the manuscript. DP collected data and reviewed the manuscript. JA reviewed the literature, revised the manuscript and supervised the write-up.
Competing interests: None declared.
Patient consent: Obtained.
Provenance and peer review: Not commissioned; externally peer reviewed.
References
- 1.Ayuk J. Does pituitary radiotherapy increase the risk of stroke and, if so, what preventative actions should be taken? Clin Endocrinol (Oxf) 2012;76: 328–31. doi:10.1111/j.1365-2265.2011.04300.x [DOI] [PubMed] [Google Scholar]
- 2.Karavitaki N, Cudlip S, Adams CB et al. Craniopharyngiomas. Endocr Rev 2006;27:371–97. [DOI] [PubMed] [Google Scholar]
- 3.Gleeson H, Amin R, Maghnie M. ‘Do no harm’: management of craniopharyngioma. Eur J Endocrinol 2008;159(Suppl 1):S95–9. doi:10.1530/EJE-08-0400 [DOI] [PubMed] [Google Scholar]