Pregled bibliografske jedinice broj: 786794
From erectile dysfunction to brain subependymoma: a case report
From erectile dysfunction to brain subependymoma: a case report // Endocrine Abstracts (2015) 37 EP1197
Dublin, Irska, 2015. str. 1-1 doi:10.1530/endoabs.37.EP1197 (poster, međunarodna recenzija, sažetak, ostalo)
CROSBI ID: 786794 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
From erectile dysfunction to brain subependymoma: a case report
Autori
Bačun, Tatjana ; Kibel, Aleksandar ; Degmečić, Dunja ; Zibar, Karin ; Pavić, Roman
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo
Izvornik
Endocrine Abstracts (2015) 37 EP1197
/ - , 2015, 1-1
Skup
European Congress of Endocrinology
Mjesto i datum
Dublin, Irska, 16.05.2015. - 20.05.2015
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
erectile dysfunction ; endocrine disease ; prolactin ; testosterone ; brain tumor ; subependymoma
Sažetak
Introduction: Endocrinopathies are rare causes of erectile dysfunction and previously cases of hyperprolactinaemia and pituitary adenomas have been reported. Case report: We present the clinical case of a 27-year old male, married for 4 years with no children, presented with possible infertility and erectile dysfunction which was previously interpreted as caused by a poor social and psychological situation in the family. After additional endocrinological (mildly elevated prolactin levels and reduced levels of testosterone) and radiological (skull X-ray, CT scan and MRI) an underlying subependymoma was discovered. The subependymoma was expanding in the sellar and suprasellar regions and pressing against the pituitary gland. The patient experienced occasional periorbital and temporal headaches, loss of appetite, general weakness. A Goldman perimeter test was consistent with bitemporal hemianopia. The resulting endocrine disorder caused the problems which were subjectively at first mainly manifested as erectile dysfunction. The patient underwent a left-sided supraorbital craniotomy and complete surgical removal of the tumor at the Department of Neurosurgery. The histopathology findings described a subependymoma (G II). One year after surgery, the patient was in good general condition, but with bitemporal hemianopia, with atrophy of the right optic nerve and complete loss of vision in his right eye, panhypopituitarism and impotence. Two years later, with hormone replacement therapy (desmopressin, hydrocortisone, levothyroxine, testosterone undecanoate) there was no sexual dysfunction. Conclusions: The case is an educative example about the necessity to keep possible intracranial lesions in mind when starting the workup of a patient presenting with erectile dysfunction. It may be of broad clinical interest not only for endocrinologists, but for practitioners in various fields.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Klinički bolnički centar Osijek,
Klinika za traumatologiju,
Medicinski fakultet, Osijek
Profili:
Aleksandar Kibel
(autor)
Tatjana Bačun
(autor)
Dunja Degmečić
(autor)
Roman Pavić
(autor)
Karin Zibar Tomšić
(autor)