Evidence map›Paper›PMID 42730490›Full record

ArticleSkin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI)2026

Advanced Imaging Techniques for Early in-Vivo Discrimination of Fibrofolliculomas in Birt-Hogg-Dubé Syndrome.

Maximilian Deußing, Daniela Hartmann, Pontus Mertsch, Charlotte Gust, Michael J Flaig, Marlene Reithmair, Julia Hoefele, Elke C Sattler

Abstract read
In one paragraph

Article in Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Maximilian DeußingDepartment of Dermatology and Allergy, LMU University Hospital, LMU Munich, Munich, Germany.ORCID https://orcid.org/0000-0003-4935-9877
Daniela HartmannDepartment of Dermatology and Allergy, LMU University Hospital, LMU Munich, Munich, Germany.ORCID https://orcid.org/0000-0002-1002-8133
Pontus MertschDepartment of Medicine V, University Hospital, LMU Munich, München, Germany.
Charlotte GustDepartment of Dermatology and Allergy, LMU University Hospital, LMU Munich, Munich, Germany.
Michael J FlaigDepartment of Dermatology and Allergy, LMU University Hospital, LMU Munich, Munich, Germany.
Marlene ReithmairInstitute of Human Genetics, LMU University Hospital, LMU Munich, Munich, Germany.ORCID https://orcid.org/0000-0002-9113-9643
Julia Hoefele *Institute of Human Genetics, LMU University Hospital, LMU Munich, Munich, Germany.ORCID https://orcid.org/0000-0002-7917-7129
Elke C Sattler *Department of Dermatology and Allergy, LMU University Hospital, LMU Munich, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBirt-Hogg-Dubé syndrome (BHDS) is a rare genetic tumor syndrome characterized by cutaneous fibrofolliculoma and trichodiscomas, lung bullae with an elevated risk of spontaneous pneumothorax and renal cell cancer.

objectivesDue to rareness of the disease, clinical symptoms and cutaneous manifestations are often misjudged, resulting in delayed medical diagnosis and considerable health risks for patients and their families. Accurate discrimination of fibrofolliculomas from other non-malignant skin tumors can be crucial for early diagnosis and appropriate management of BHDS. In addition, they may clinically overlap with adnexal or follicular papules seen in other rare genodermatoses, including facial angiofibromas in tuberous sclerosis complex, trichilemmomas in Cowden syndrome/PTEN hamartoma tumor syndrome, and trichoepitheliomas in CYLD cutaneous syndrome.

methodsIn this study, skin lesions from 15 BHDS patients with genetic confirmed disease-causing variants in FLCN underwent reflectance confocal microscopy (RCM) and Line-Field Confocal Optical Coherence Tomography (LC-OCT) to systematically analyse the morphologic and microstructural features of fibrofolliculomas.

resultsIn RCM a dilated follicular unit was seen in 12/15 cases (80%), while in LC-OCT this feature was seen in 13/15 (87%). The characteristic round, onion-like shaped hyperreflective structures with a well-demarcated perifollicular halo, corresponding to the histopathological features of branching chords and strands of epithelial cells was seen in all cases (RCM and LC-OCT 100%), aiding clinicians in identifying fibrofolliculomas.

conclusionAdvanced imaging techniques provide a non-invasive approach for early diagnosis of fibrofolliculomas. Therefore, RCM and especially LC-OCT may be promising tools for enhancing the diagnostic precision and sufficient clinical management of Birt-Hogg-Dubé syndrome.

Indexed as

Birt-Hogg-Dube SyndromeSkin NeoplasmsAdolescentAdultChildDiagnosis, DifferentialFemaleHumansMaleMicroscopy, ConfocalMiddle AgedProto-Oncogene ProteinsTomography, Optical CoherenceTumor Suppressor ProteinsYoung AdultFLCN protein, humanProto-Oncogene ProteinsTumor Suppressor Proteinshistopathologyline‐field confocal OCTnon‐invasive imagingrare skin diseases

Identifiers

PMID42730490
PMCPMC13570421

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.