Evidence map›Paper›PMID 34807360›Full record

ArticlePituitary2022

A study on clinical outcomes of Rathke's cleft cyst in patients managed conservatively.

Gigi Y C Chong, Kathryn C B Tan, Emmy Y F Lau, Alta Y T Lai, Kenyon K Y Man, T M Chan, Warren K W Leung, Jenny Y Y Leung

Abstract read
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In one paragraph

Article in Pituitary, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Rathke's cleft cyst: From history to molecular genetics.Reviews in endocrine & metabolic disorders · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Gigi Y C ChongDepartment of Medicine and Geriatrics, Ruttonjee Hospital, Wan Chai, Hong Kong. gigicyc4@gmail.com.ORCID http://orcid.org/0000-0002-1361-8008
Kathryn C B TanDepartment of Medicine, Queen Mary Hospital, Pokfulam, Hong Kong.
Emmy Y F LauDepartment of Medicine, Pamela Youde Nethersole Eastern Hospital, Chai Wan, Hong Kong.
Alta Y T LaiDepartment of Radiology, Pamela Youde Nethersole Eastern Hospital, Chai Wan, Hong Kong.
Kenyon K Y ManDepartment of Radiology, Queen Mary Hospital, Pokfulam, Hong Kong.
T M ChanDepartment of Radiology, Ruttonjee Hospital, Wan Chai, Hong Kong.
Warren K W LeungDepartment of Radiology, Pamela Youde Nethersole Eastern Hospital, Chai Wan, Hong Kong.
Jenny Y Y LeungDepartment of Medicine and Geriatrics, Ruttonjee Hospital, Wan Chai, Hong Kong.
Pamela Youde Nethersole Eastern Hospital · CNRuttonjee Hospital · CNQueen Mary Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe primary objective was to investigate the clinical presentation, hormonal dysfunction, imaging characteristics and natural history of RCCs that were managed conservatively. Secondary objective was to identify factors associated with cyst progression.

methodsA retrospective review of patients with the clinical diagnosis of RCC-identified from word search from radiology reports that were followed up from January 1999 to March 2019 was performed. The demographics, clinical data, radiological features and outcomes were reviewed and analyzed.

results105 patients were identified with a median follow up of 6 years. 68 patients (64.8%) were managed conservatively from diagnosis till last follow up while 37 patients (35.2%) underwent surgery, with 26 operated at time of diagnosis and 11 operated upon monitoring. For patients managed conservatively from diagnosis till last follow up, incidental finding was the most common presentation. 19.1% had either one or more axes of hormonal dysfunction, with hypogonadism and hypocortisolemia being the commonest ones. Imaging features were variable. 66.2% of patients had T2W hyperintensity on MRI. Pathognomonic feature of intracystic nodule was present in only 14.7% of patients. Among the 79 patients with repeated MRI imaging (68 from conservative group and 11 from surgical group), 32.9% of patients developed cyst progression while 67.1% had either static disease or regression in size of RCC. Median time to progression of cyst was 14 months. Longer median follow up duration and presence of pituitary stalk displacement at presentation were associated with cyst progression. Only one patient developed new endocrine dysfunction.

conclusion2/3 of the RCCs had static disease or even regression in the size of the cyst. They rarely gave rise to additional endocrine dysfunction by adopting observant approach. Cyst progression was demonstrated in 1/3 of patients. Conservative treatment remained a reasonable treatment for patients without significant symptoms.

Indexed as

Central Nervous System CystsPituitary NeoplasmsHumansMagnetic Resonance ImagingPituitary GlandRetrospective StudiesTreatment OutcomeHypopituitarismPituitary glandPituitary macroadenomaPituitary microadenomaRathke's cleft cyst

Identifiers

PMID34807360
OpenAlexW3217227457

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.