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Natural history and surgical outcome of Rathke's cleft cysts: A study from the Swedish Pituitary Registry
Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden; Department of Endocrinology, Karolinska University Hospital, Stockholm, Sweden.
Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden; Department of Endocrinology, Karolinska University Hospital, Stockholm, Sweden.
Department of Medical Sciences, Endocrinology and Mineral Metabolism, Uppsala University, Uppsala, Sweden; Uppsala University Hospital, Uppsala, Sweden.
Department of Medical Sciences, Endocrinology and Mineral Metabolism, Uppsala University, Uppsala, Sweden; Uppsala University Hospital, Uppsala, Sweden.
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2022 (English)In: Clinical Endocrinology, ISSN 0300-0664, E-ISSN 1365-2265, Vol. 96, no 1, p. 54-61Article in journal (Refereed) Published
Abstract [en]

OBJECTIVE: Rathke's cleft cysts are benign, embryological remnants in the pituitary gland. The majority of them are small and asymptomatic but a few may become large, and cause mass effects, pituitary hormone deficiencies and visual impairment. Recommendations for the follow-up of Rathke's cleft cysts vary since data on the natural history are sparse.

PATIENTS AND DESIGN: Data at diagnosis and at 1, 5 and 10 years for patients with a Rathke's cleft cyst (434 at diagnosis, 317 females) were retrieved from the Swedish Pituitary Registry. Cysts ≤3 mm in diameter were excluded from the study.

MEASUREMENTS: Data included demographics, cyst size, pituitary function, visual defects and surgery.

RESULTS: The mean age at diagnosis was 45 years. In patients with cysts <10 mm in diameter (n = 204) 2.9% had pituitary hormone deficiencies and 2% had visual field impairments. Cyst size did not progress during the 5 years. Cysts with a diameter of ≥10 mm that were not operated (n = 174) decreased in size over the years (p < .01). Pituitary hormone deficiencies and visual impairments were more frequent (18% and 5.7%, respectively) but were stable over time. Transphenoidal surgery was performed in 56 patients of whom 51 underwent surgery before the 1-year follow-up. The mean cyst diameter at diagnosis was 18 mm (range: 9─30 mm), 36% had pituitary hormone deficiency, 45% had visual field defects and 20% had impaired visual acuity. One year after surgery 60% had no cyst remnants, 50% had a pituitary deficiency, 26% had visual field defects and 12% had impaired visual acuity. No major changes were observed after 5 years. Twelve of the operated patients had a follow-up at 10 years, in eight the cyst remnants or recurrences increased in size over time (p < .05).

CONCLUSIONS: Rathke's cleft cysts with a size less than 10 mm rarely grow and our results indicate that radiological follow-up can be restricted to 5 years. In contrast, progression of postoperative remnants or recurrent cysts is more likely and require long-term follow-up.

Place, publisher, year, edition, pages
Wiley-Blackwell Publishing Inc., 2022. Vol. 96, no 1, p. 54-61
Keywords [en]
Rathke's cleft cyst, cyst size, hypopituitarism, pituitary, transphenoidal surgery, visual impairment
National Category
Endocrinology and Diabetes
Identifiers
URN: urn:nbn:se:oru:diva-95304DOI: 10.1111/cen.14622ISI: 000713307500001PubMedID: 34724249Scopus ID: 2-s2.0-85118404648OAI: oai:DiVA.org:oru-95304DiVA, id: diva2:1608316
Available from: 2021-11-03 Created: 2021-11-03 Last updated: 2024-01-02Bibliographically approved

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Wahlberg, Jeanette

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