Prolactinoma in childhood and adolescence-Tumour size at presentation predicts management strategy: Single centre series and a systematic review and meta-analysis

被引:14
作者
Arya, Ved Bhushan [1 ]
Aylwin, Simon J. B. [2 ]
Hulse, Tony [3 ]
Ajzensztejn, Michal [3 ]
Kalitsi, Jennifer [1 ]
Kalogirou, Nicolas [1 ]
Bodi, Istvan [4 ]
Thomas, Nick [5 ]
Hampton, Tim [6 ]
Kapoor, Ritika R. [1 ,7 ]
Buchanan, Charles R. [1 ]
机构
[1] Kings Coll Hosp NHS Fdn Trust, Variety Club Childrens Hosp, Paediat Endocrinol, London, England
[2] Kings Coll Hosp NHS Fdn Trust, Endocrinol, London, England
[3] Guys & St Thomas NHS Trust, Evelina London Childrens Hosp, Paediat Endocrinol, London, England
[4] Kings Coll Hosp NHS Fdn Trust, Neuropathol, London, England
[5] Kings Coll Hosp NHS Fdn Trust, Neurosurg, London, England
[6] Kings Coll Hosp NHS Fdn Trust, Neuroradiol, London, England
[7] Kings Coll London, Fac Med & Life Sci, London, England
关键词
cabergoline; MEN1; meta‐ analysis; pituitary adenoma; prolactinoma; systematic review; PITUITARY-ADENOMAS; CLINICAL PRESENTATION; PUBERTAL CHANGES; CHILDREN; GROWTH; DIAGNOSIS; SURGERY; PATTERN;
D O I
10.1111/cen.14394
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective To report the clinical presentation, management and outcomes of young patients with prolactinomas (<20 years) and conduct a systematic review and meta-analysis. Patients and Design Clinical, biochemical and radiological data (1996-2018) were collected from our centre. A systematic review and meta-analysis of published literature (1994-2019) on prolactinoma (age <20 years) were conducted. Both random and fixed effects meta-analysis were used to pool outcomes across studies. Results 1 Case series Twenty-two patients (14 females) were identified; median age at diagnosis 15.7 years (range 13-19); 12 patients (6 females) had a macroprolactinoma. Seven patients (macroprolactinoma-6) had associated pituitary hormone deficiencies at presentation. Five patients (4 males) underwent surgical resection due to poor response to cabergoline or apoplexy. Patients undergoing surgery had larger tumours (p < .02) and higher serum prolactin concentration (p < .005). All patients with macroprolactinoma >20 mm required surgical intervention. Results 2 Systematic review and meta-analysis We selected 11 studies according to strict inclusion criteria describing 275 patients. Macroprolactinoma was more common in girls (78.7% [95% CI 70.5-85.9]) than boys and was more frequent than microprolactinoma (56.6% [95% CI 48.4-64.5]). In males, only 6/57 (10.5%) of tumours were microprolactinoma as compared to 102/198 (51.5%) microprolactinoma in females (risk difference -0.460; [95% CI -0.563 to -0.357]; p < .001). Surgery was first-line therapy in 18.9% patients, with another 15.4% requiring it as a second line (overall 31.3%). Conclusions Macroprolactinoma, particularly if >20 mm, usually requires multimodal therapy including surgical intervention. While overall prolactinomas in <20 years age group are more common in females, the proportion of macroprolactinoma vs microprolactinoma is greater in males, particularly for large invasive tumours. Microprolactinoma is a rare diagnosis in adolescent males.
引用
收藏
页码:413 / 423
页数:11
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