Definition and research guide
This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.
Content available: 4 complete abstracts (941 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.
Definition
A non-neoplastic mass of keratin-producing squamous epithelium, frequently occurring in the meninges; bones of the skull, and most commonly in the middle ear and mastoid region. Cholesteatoma can be congenital or acquired. Cholesteatoma is not a tumor nor is it associated with high cholesterol.
Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.
Also known as: Cholesteatomas.
Where it fits in the MeSH classification
- Broader topics
- Keratosis
- Narrower topics
- Cholesteatoma, Middle Ear
Related concepts
- Epithelium
- Meninges
- Middle Ear
- Mastoid
- Cholesterol
Research landscape
PubMed indexes 7,055 records tagged with the MeSH heading “Cholesteatoma” (counts retrieved 2026-11-04). 921 of them (13.1%) were published from 2020 onward, and the busiest period so far is through 1999 with 3,640 records.
Reviews account for 555 records (7.9%) and meta-analyses for 37. Randomized controlled trials number 24 (0.3%) as a share of all records on the topic. Randomized trials make up only a small share of this literature, so much of what is known comes from laboratory, observational or descriptive work.
Show the data
| Period | Records |
|---|---|
| through 1999 | 3,640 |
| 2000-2009 | 1,136 |
| 2010-2019 | 1,358 |
| 2020 onward | 921 |
Publication-type chart data
| Type | Records | Share |
|---|---|---|
| Reviews | 555 | 7.9% |
| Meta-analyses | 37 | 0.5% |
| Randomized controlled trials | 24 | 0.3% |
Method: PubMed query "Cholesteatoma"[MeSH Terms] with publication-type and date filters, retrieved 2026-11-04.
Reading the evidence in bones, joints, muscles and skin
Joint, bone, muscle and skin conditions are often judged by pain scores, function questionnaires, imaging or photographs, and symptoms can fluctuate, so placebo response and natural improvement matter. Imaging changes are common in people without symptoms. Nothing on this page is advice about treatment. Check how outcomes were measured, whether the comparison group received a placebo or usual care, and how long the benefit lasted.
Evidence from open-access studies
These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.
| Study / authors | Year | Source label / design | Europe PMC citations | Licence / source |
|---|---|---|---|---|
| Updates and knowledge gaps in cholesteatoma research | 2015 | Review article Design not recorded in structured metadata | 151 | cc by PMID 25866816 · DOI · PMC4381684 |
| Cholesteatoma labyrinthine fistula: prevalence and impact | 2019 | Research article Design not recorded in structured metadata | 26 | cc by PMID 29599061 · DOI · PMC9452264 |
| Mastoid cavity obliteration leads to a clinically significant improvement in health-related quality of life | 2020 | Research article Design not recorded in structured metadata | 24 | cc by PMID 32144569 · DOI · PMC7198475 |
| MRI-DWI detection of residual cholesteatoma: moving toward an optimum follow-up scheme | 2025 | Research article Design not recorded in structured metadata | 6 | cc by PMID 39269619 · DOI · PMC11805829 |
Updates and knowledge gaps in cholesteatoma research [1]
Abstract reading summary — source excerpts
- Opening excerpt
- The existence of acquired cholesteatoma has been recognized for more than three centuries; however, the nature of the disorder has yet to be determined.
- Closing excerpt
- We also consider issues related to the classification, epidemiology, histopathology, clinical presentation, and complications of acquired cholesteatoma and examine current diagnosis and management strategies in detail.
- Interpretation limits
- Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (158 words)
The existence of acquired cholesteatoma has been recognized for more than three centuries; however, the nature of the disorder has yet to be determined. Without timely detection and intervention, cholesteatomas can become dangerously large and invade intratemporal structures, resulting in numerous intra- and extracranial complications. Due to its aggressive growth, invasive nature, and the potentially fatal consequences of intracranial complications, acquired cholesteatoma remains a cause of morbidity and death for those who lack access to advanced medical care. Currently, no viable nonsurgical therapies are available. Developing an effective management strategy for this disorder will require a comprehensive understanding of past progress and recent advances. This paper presents a brief review of background issues related to acquired middle ear cholesteatoma and deals with practical considerations regarding the history and etymology of the disorder. We also consider issues related to the classification, epidemiology, histopathology, clinical presentation, and complications of acquired cholesteatoma and examine current diagnosis and management strategies in detail.
Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 25866816 · DOI · PMC4381684
Cholesteatoma labyrinthine fistula: prevalence and impact [2]
Abstract reading summary — source excerpts
- Opening excerpt
- IntroductionLabyrinthine fistula is one of the most common complications associated with cholesteatoma.
- Closing excerpt
- Sensorineural hearing loss can occur post-surgically, even in previously unaffected patients despite the technique employed.
- Interpretation limits
- Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (298 words)
IntroductionLabyrinthine fistula is one of the most common complications associated with cholesteatoma. It represents an erosive loss of the endochondral bone overlying the labyrinth. Reasons for cholesteatoma-induced labyrinthine fistula are still poorly understood.ObjectiveEvaluate patients with cholesteatoma, in order to identify possible risk factors or clinical findings associated with labyrinthine fistula. Secondary objectives were to determine the prevalence of labyrinthine fistula in the study cohort, to analyze the role of computed tomography and to describe the hearing results after surgery.MethodsThis retrospective cohort study included patients with an acquired middle ear cholesteatoma in at least one ear with no prior surgery, who underwent audiometry and tomographic examination of the ears or surgery at our institution. Hearing results after surgery were analyzed according to the labyrinthine fistula classification and the employed technique.ResultsWe analyzed a total of 333 patients, of which 9 (2.7%) had labyrinthine fistula in the lateral semicircular canal. In 8 patients, the fistula was first identified on image studies and confirmed at surgery. In patients with posterior epitympanic and two-route cholesteatomas, the prevalence was 5.0%; and in cases with remaining cholesteatoma growth patterns, the prevalence was 0.6% (p=0.16). In addition, the prevalence ratio for labyrinthine fistula between patients with and without vertigo was 2.1. Of patients without sensorineural hearing loss before surgery, 80.0% remained with the same bone conduction thresholds, whereas 20.0% progressed to profound hearing loss. Of patients with sensorineural hearing loss before surgery, 33.33% remained with the same hearing impairment, whereas 33.33% showed improvement of the bone conduction thresholds' Pure Tone Average.ConclusionLabyrinthine fistula must be ruled out prior to ear surgery, particularly in cases of posterior epitympanic or two-route cholesteatoma. Computed tomography is a good diagnostic modality for lateral semicircular canal fistula. Sensorineural hearing loss can occur post-surgically, even in previously unaffected patients despite the technique employed.
Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 29599061 · DOI · PMC9452264
Mastoid cavity obliteration leads to a clinically significant improvement in health-related quality of life [3]
Abstract reading summary — source excerpts
- Opening excerpt
- ObjectiveTo assess the change in health-related quality of life (HRQoL) in patients undergoing mastoid cavity obliteration.
- Closing excerpt
- As a clinical implication, we provide evidence for a substantial subjective benefit of the surgical obliteration of a symptomatic mastoid cavity and, therefore, encourage this surgical procedure.
- Interpretation limits
- Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (263 words)
ObjectiveTo assess the change in health-related quality of life (HRQoL) in patients undergoing mastoid cavity obliteration.MethodsPatients who had undergone canal wall-down mastoidectomy for chronic otitis media with creation of a persistent mastoid cavity and underwent revision tympanomastoid surgery including mastoid cavity obliteration using autologous material were included. Audiological measurements including air conduction (AC) and bone conduction (BC) pure-tone averages (PTA) and the air-bone gap (ABG) were assessed. Health-related Quality of Life (HRQoL) was assessed by the Zurich Chronic Middle Ear Inventory (ZCMEI-21) pre- and postoperatively.ResultsA total of 25 patients (16 females and 9 males; mean age 51.6 years, 14 right and 11 left ears) were included. Patients were reexamined after a mean follow-up period of 9.2 months (SD = 6.5) after obliteration of the mastoid cavity. Compared to the preoperative visit, patients showed a significantly reduced AC PTA at the postoperative visit (mean difference: - 4.1; SD = 10.4, p = 0.045). The mean ZCMEI-21 score changed from 31.7 (SD = 14.5) preoperatively to 17.4 (SD = 15.1) postoperatively (mean difference: - 14.3; SD = 19.1; p = 0.0002). The mean ZCMEI-21 score changes were neither correlated to the AC PTA shift (p = 0.60) nor to the ABG shift (p = 0.66).ConclusionsThis is the first study reporting a highly significant and clinically important improvement in HRQoL after mastoid cavity obliteration in a prospective setting. The improvement in HRQoL was not correlated to the hearing improvement. As a clinical implication, we provide evidence for a substantial subjective benefit of the surgical obliteration of a symptomatic mastoid cavity and, therefore, encourage this surgical procedure.
Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 32144569 · DOI · PMC7198475
MRI-DWI detection of residual cholesteatoma: moving toward an optimum follow-up scheme [4]
Abstract reading summary — source excerpts
- Opening excerpt
- PurposeTo analyse diagnostic accuracy of MRI-DWI in detecting residual disease after cholesteatoma surgery and propose an optimum follow-up (FU) scheme.
- Closing excerpt
- , patients < 12 yrs or patients undergoing canal wall up surgery without obliteration).
- Interpretation limits
- Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (222 words)
PurposeTo analyse diagnostic accuracy of MRI-DWI in detecting residual disease after cholesteatoma surgery and propose an optimum follow-up (FU) scheme.MethodA retrospective chart review of patients who had cholesteatoma surgery in a tertiary referral centre. 3.0 T non-echo planar diffusion weighted imaging was performed as part of routine FU or indicated on the basis of clinical suspicion of disease. Imaging outcome was verified per-operatively during a second-look procedure or ossicular chain reconstruction. Diagnostic parameters were calculated and stratified by FU length.ResultsFor the FU of 664 cholesteatoma surgeries, 1208 MRI-DWI were obtained and 235 second-look procedures were performed. Most MRI-DWI were obtained within 1.5 yrs of surgery. In this period, significantly less true positive MRI-DWI and significantly more false negative MRI-DWI for residual disease were found compared to other FU periods. Scanning after approximately 3 yrs yielded a significantly higher rate of true positive MRI-DWI, while sensitivity surpassed 80%. Younger patients had a higher risk of developing residual disease. Patients undergoing canal wall up surgery, as well as patients ConclusionA novel radiologic FU scheme for detecting residual disease is suggested for stable ears after cholesteatoma surgery: standard MRI-DWI approximately 3 and 5 yrs after primary surgery, as well as MRI-DWI after approximately 9 yrs for patients with specific risk factors (i.e., patients < 12 yrs or patients undergoing canal wall up surgery without obliteration).
Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 39269619 · DOI · PMC11805829
Key reviews and meta-analyses
The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.
- Research article EAONO/JOS Joint Consensus Statements on the Definitions, Classification and Staging of Middle Ear Cholesteatoma [5]
- Research article Etiopathogenesis of cholesteatoma [6]
- Research article Surgical technique and recurrence in cholesteatoma: a meta-analysis [7]
- Research article Neuroradiology of cholesteatomas [8]
- Research article Etiopathogenesis of acquired cholesteatoma: prominent theories and recent advances in biomolecular research [9]
- Research article Cholesteatoma Pearls: Practical Points and Update [10]
References
- Kuo CL, Shiao AS, Yung M, Sakagami M, Sudhoff H, Wang CH, et al.. Updates and knowledge gaps in cholesteatoma research. . 2015. PMID 25866816 · DOI · PMC4381684
- Rosito LPS, Canali I, Teixeira A, Silva MN, Selaimen F, Costa SSD. Cholesteatoma labyrinthine fistula: prevalence and impact. . 2019. PMID 29599061 · DOI · PMC9452264
- Weiss NM, Bächinger D, Botzen J, Großmann W, Mlynski R. Mastoid cavity obliteration leads to a clinically significant improvement in health-related quality of life. . 2020. PMID 32144569 · DOI · PMC7198475
- Eggink MC, de Wolf MJF, Ebbens FA, de Win MML, Dikkers FG, van Spronsen E. MRI-DWI detection of residual cholesteatoma: moving toward an optimum follow-up scheme. . 2025. PMID 39269619 · DOI · PMC11805829
- Yung M, Tono T, Olszewska E, Yamamoto Y, Sudhoff H, Sakagami M, et al.. EAONO/JOS Joint Consensus Statements on the Definitions, Classification and Staging of Middle Ear Cholesteatoma. J Int Adv Otol. 2017. PMID 28059056 · DOI
- Olszewska E, Wagner M, Bernal-Sprekelsen M, Ebmeyer J, Dazert S, Hildmann H, et al.. Etiopathogenesis of cholesteatoma. Eur Arch Otorhinolaryngol. 2004. PMID 12835944 · DOI
- Tomlin J, Chang D, McCutcheon B, Harris J. Surgical technique and recurrence in cholesteatoma: a meta-analysis. Audiol Neurootol. 2013. PMID 23327931 · DOI
- Baráth K, Huber AM, Stämpfli P, Varga Z, Kollias S. Neuroradiology of cholesteatomas. AJNR Am J Neuroradiol. 2011. PMID 20360335 · DOI · PMC7965719
- Kuo CL. Etiopathogenesis of acquired cholesteatoma: prominent theories and recent advances in biomolecular research. Laryngoscope. 2015. PMID 25123251 · DOI
- Castle JT. Cholesteatoma Pearls: Practical Points and Update. Head Neck Pathol. 2018. PMID 30069838 · DOI · PMC6081285
About this article
- Sources
- NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
- Verification
- Every reference was resolved against PubMed on 2026-11-04; title, year and DOI matched.
- Review state
- automated source verified; no human expert review has been recorded yet.
- Version
- 1, last updated 2026-11-04.
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Evidence strength
EvidenceHelix's computed view of the study designs behind this topic: how common meta-analyses, randomized trials and reviews are, how recent the literature is, and a plain-language reading. It describes the design mix of the literature. It is not a quality appraisal of any study, and it is not medical advice.