Silent corticotroph adenomas have unique recurrence characteristics compared with other nonfunctioning pituitary adenomas
Silent corticotroph adenomas have unique recurrence characteristics compared with other nonfunctioning pituitary adenomas
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DOI:
10.1111/j.1365-2265.2009.03673.x
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发表时间:
2010-05-01
影响因子:
3.2
通讯作者:
Kim, Seong Yeon
中科院分区:
文献类型:
--
作者:
Cho, Hwa Young;Cho, Sun Wook;Kim, Seong Yeon
P>ObjectiveThe prevalence of silent corticotroph adenomas (SCAs) is not rare among nonfunctioning pituitary adenomas (NFPAs); however, it is unknown whether the clinical significance of SCAs differs from that of NFPAs without ACTH immunoreactivity (non-SCAs). Our goal was to compare the clinical characteristics and natural history between patients with SCAs and non-SCAs.Design/patientsWe reviewed the medical records of all patients who underwent transsphenoidal surgery for NFPAs from January 1990 to October 2007 at the Seoul National University Hospital.MeasurementsWe analysed whether clinical manifestations at diagnosis, postoperative recurrence rate and recurrence characteristics differed between SCA and non-SCA patients.ResultsIn total, 28 patients with SCAs and 134 patients with non-SCAs were analysed. The mean age at the time of diagnosis was 44 years (range, 13-67 years) in the SCA group and 50 years (18-79 years) in the non-SCA group (P = 0 center dot 026), with respective follow-up periods of 5 center dot 2 (range, 1 center dot 0-16 center dot 0 years) and 4 center dot 2 years (0 center dot 5-16 center dot 1 years) (P = 0 center dot 255). Overall recurrence rates of SCAs and non-SCAs were 25 center dot 0% and 26 center dot 9% respectively (P = 0 center dot 839). More than two recurrences (P = 0 center dot 001) and recurrence after more than 5 years (P = 0 center dot 040) were associated with SCAs. Multiple recurrences of SCAs were confined to younger patients.ConclusionThe overall recurrence rate was similar between SCAs and non-SCAs. However, young patients with SCAs had a higher frequency of multiple and late recurrences, which showed more aggressive tumour behaviour. Therefore, we suggest that patients with SCAs, especially patients diagnosed at a young age, require careful long-term monitoring.