The clinical characteristics, presentation, and treatment outcomes of prolactinomas at Groote Schuur Hospital

dc.contributor.advisorDave, J A
dc.contributor.authorAbdalla, Mohamed Abdalla Mansour
dc.date.accessioned2021-07-13T10:54:38Z
dc.date.available2021-07-13T10:54:38Z
dc.date.issued2021
dc.date.updated2021-07-13T10:24:39Z
dc.description.abstractBackground: Prolactin-secreting tumours( prolactinomas) are the commonest type of pituitary tumour, accounting for approximately 30 to 40 %% of all pituitary adenomas. Although there is ample epidemiologic and clinic data from Industrialised countries there remains sparse data from Africa. Specifically, the clinical presentation, and hormonal deficiencies and treatment outcomes in the South Africa have not been described. Methods: A retrospective study of all patients with a diagnosis of prolactinoma attending the Endocrine and Pituitary Clinics at Groote Schuur Hospital over a 12-month period, between March 2019-March 2020. Patients folders were reviewed to retrieve the following information: demographic data, clinical presentation, clinical signs, prolactinoma phenotype, hormonal deficiencies, treatment modalities and clinical outcomes. Results: Over a 12-month period 52 patients were included in this study, females 73% (n=38), mean age of all participants was 46.1 ± 14.6 years. A macroprolactinoma was present in 67.3% (n=35) of patients and 32.7% (n=17) of patients had a microprolactinoma. In the macroprolactinoma group: the common presenting symptoms were headache 88.6% (n=33), altered vision 40% (n=14) and , in females, amenorrhoea 63.6% (n=14) but a cranial nerve palsy 17.1% (n=6) and apoplexy 5.7% (n=2) were uncommon. . In the microprolactinoma group the common presenting symptoms included amenorrhoea 75% (n=12), galactorrhoea 70.6% (n=12), headache 64.7% (n=11). On presentation the majority of patients with a macroadenoma had at least one hormonal abnormality with hypogonadism 73.1% (n=19) being most common, followed by hypothyroidism 53.8% (n=14) and hypoadrenalism 30% (n=8). Over 50% of patients with a giant adenoma had panhypopituitarism with hypogonadism in 100%, hypothyroidism in 77.8% (n=7) and hypoadrenalism in 66.7% (n=6). Hormonal deficiencies in the microadenoma group on presentation included hypogonadism 64.7% (n=11), hypothyroidism 35.3 (n=6) and one patient had hypoadrenalism. All patients received medical treatment, however, in the macroadenoma group 4 patients required surgical debulking of the tumour, 3 patients required a ventriculo-peritoneal (VP) shunt for hydrocephalus and 2 patients required radiation. After a median follow-up of 46.5 months, the median prolactin level decreased from 322.5 ug/l (94.0-4282.0) at presentation to 17.5 ug/l (8.6-82.5) at follow-up. In parallel there was a reduction of 12.2 ±9.7 mm in tumour size after a mean of 59.8 ±53.3 months. There was resolution of hypogonadism in 56.4% (n=22), of hypothyroidism in 2.7% (n=2) and hypoadrenalism only resolved in 1 patient. Conclusions: Most patients with a prolactinoma are symptomatic and have at least one hormone deficiency on presentation. With medical management most patients experienced a reduction in prolactin levels and tumour size. . This was associated with the resolution of hypogonadism in the majority, however, hypothyroidism and hypoadrenalism are unlikely to resolve despite a reduction in tumour size.
dc.identifier.apacitationAbdalla, M. A. M. (2021). <i>The clinical characteristics, presentation, and treatment outcomes of prolactinomas at Groote Schuur Hospital</i>. (). ,Faculty of Health Sciences ,Division of Endocrinology and Diabetology. Retrieved from http://hdl.handle.net/11427/33620en_ZA
dc.identifier.chicagocitationAbdalla, Mohamed Abdalla Mansour. <i>"The clinical characteristics, presentation, and treatment outcomes of prolactinomas at Groote Schuur Hospital."</i> ., ,Faculty of Health Sciences ,Division of Endocrinology and Diabetology, 2021. http://hdl.handle.net/11427/33620en_ZA
dc.identifier.citationAbdalla, M.A.M. 2021. The clinical characteristics, presentation, and treatment outcomes of prolactinomas at Groote Schuur Hospital. . ,Faculty of Health Sciences ,Division of Endocrinology and Diabetology. http://hdl.handle.net/11427/33620en_ZA
dc.identifier.ris TY - Master Thesis AU - Abdalla, Mohamed Abdalla Mansour AB - Background: Prolactin-secreting tumours( prolactinomas) are the commonest type of pituitary tumour, accounting for approximately 30 to 40 %% of all pituitary adenomas. Although there is ample epidemiologic and clinic data from Industrialised countries there remains sparse data from Africa. Specifically, the clinical presentation, and hormonal deficiencies and treatment outcomes in the South Africa have not been described. Methods: A retrospective study of all patients with a diagnosis of prolactinoma attending the Endocrine and Pituitary Clinics at Groote Schuur Hospital over a 12-month period, between March 2019-March 2020. Patients folders were reviewed to retrieve the following information: demographic data, clinical presentation, clinical signs, prolactinoma phenotype, hormonal deficiencies, treatment modalities and clinical outcomes. Results: Over a 12-month period 52 patients were included in this study, females 73% (n=38), mean age of all participants was 46.1 ± 14.6 years. A macroprolactinoma was present in 67.3% (n=35) of patients and 32.7% (n=17) of patients had a microprolactinoma. In the macroprolactinoma group: the common presenting symptoms were headache 88.6% (n=33), altered vision 40% (n=14) and , in females, amenorrhoea 63.6% (n=14) but a cranial nerve palsy 17.1% (n=6) and apoplexy 5.7% (n=2) were uncommon. . In the microprolactinoma group the common presenting symptoms included amenorrhoea 75% (n=12), galactorrhoea 70.6% (n=12), headache 64.7% (n=11). On presentation the majority of patients with a macroadenoma had at least one hormonal abnormality with hypogonadism 73.1% (n=19) being most common, followed by hypothyroidism 53.8% (n=14) and hypoadrenalism 30% (n=8). Over 50% of patients with a giant adenoma had panhypopituitarism with hypogonadism in 100%, hypothyroidism in 77.8% (n=7) and hypoadrenalism in 66.7% (n=6). Hormonal deficiencies in the microadenoma group on presentation included hypogonadism 64.7% (n=11), hypothyroidism 35.3 (n=6) and one patient had hypoadrenalism. All patients received medical treatment, however, in the macroadenoma group 4 patients required surgical debulking of the tumour, 3 patients required a ventriculo-peritoneal (VP) shunt for hydrocephalus and 2 patients required radiation. After a median follow-up of 46.5 months, the median prolactin level decreased from 322.5 ug/l (94.0-4282.0) at presentation to 17.5 ug/l (8.6-82.5) at follow-up. In parallel there was a reduction of 12.2 ±9.7 mm in tumour size after a mean of 59.8 ±53.3 months. There was resolution of hypogonadism in 56.4% (n=22), of hypothyroidism in 2.7% (n=2) and hypoadrenalism only resolved in 1 patient. Conclusions: Most patients with a prolactinoma are symptomatic and have at least one hormone deficiency on presentation. With medical management most patients experienced a reduction in prolactin levels and tumour size. . This was associated with the resolution of hypogonadism in the majority, however, hypothyroidism and hypoadrenalism are unlikely to resolve despite a reduction in tumour size. DA - 2021_ DB - OpenUCT DP - University of Cape Town KW - Hyperprolactinemia KW - hypogonadism KW - Prolactin KW - Prolactinoma LK - https://open.uct.ac.za PY - 2021 T1 - The clinical characteristics, presentation, and treatment outcomes of prolactinomas at Groote Schuur Hospital TI - The clinical characteristics, presentation, and treatment outcomes of prolactinomas at Groote Schuur Hospital UR - http://hdl.handle.net/11427/33620 ER - en_ZA
dc.identifier.urihttp://hdl.handle.net/11427/33620
dc.identifier.vancouvercitationAbdalla MAM. The clinical characteristics, presentation, and treatment outcomes of prolactinomas at Groote Schuur Hospital. []. ,Faculty of Health Sciences ,Division of Endocrinology and Diabetology, 2021 [cited yyyy month dd]. Available from: http://hdl.handle.net/11427/33620en_ZA
dc.language.rfc3066eng
dc.publisher.departmentDivision of Endocrinology and Diabetology
dc.publisher.facultyFaculty of Health Sciences
dc.subjectHyperprolactinemia
dc.subjecthypogonadism
dc.subjectProlactin
dc.subjectProlactinoma
dc.titleThe clinical characteristics, presentation, and treatment outcomes of prolactinomas at Groote Schuur Hospital
dc.typeMaster Thesis
dc.type.qualificationlevelMasters
dc.type.qualificationlevelMPhil
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