Evidence map›Paper›PMID 42726111›Full record

ArticleVirchows Archiv : an international journal of pathology2026

Expression of tyrosine hydroxylase (TH) in human tumors: a tissue microarray study evaluating 18,666 tumors from 150 different tumor entities.

Florian Viehweger, Sören Schönig, Natalia Gorbokon, Maximilian Lennartz, Katharina Möller, Anne Menz, Ria Uhlig, Andreas M Luebke, Martina Kluth, Claudia Hube-Magg and 13 more

Abstract read
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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 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

23 authors.

Florian ViehwegerInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Sören SchönigInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Natalia GorbokonInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Maximilian LennartzInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Katharina MöllerInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Anne MenzInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Ria UhligInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Andreas M LuebkeInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Martina KluthInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Claudia Hube-MaggInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Andrea HinschInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Florian LutzInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Christian BernreutherInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Guido SauterInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
David DumInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Andreas H MarxDepartment of Pathology, Academic Hospital Fuerth, Fuerth, Germany.
Ronald SimonInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany. R.Simon@uke.de.ORCID http://orcid.org/0000-0003-0158-4258
Till KrechInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Till S ClauditzInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Frank JacobsenInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Eike BurandtInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Stefan SteurerInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.
Sarah MinnerInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, Hamburg, 20246, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TH immunohistochemistry (IHC) has been proposed as a sensitive and specific tool for the distinction of pheochromocytomas or paragangliomas from epithelial neuroendocrine neoplasms and tumors. However, little is known about the prevalence of TH expression in other tumor entities. To comprehensively evaluate TH expression in normal and tumor tissues, a tissue microarray containing 18,666 samples from 150 different tumor types and subtypes and 608 samples of 76 different normal tissue types were analyzed by IHC. TH immunostaining in tumors was always cytoplasmic. It was detectable in 158 (1%) of the 15,630 analyzable tumors, including 23 (0.1%) with weak, 28 (0.2%) with moderate, and 107 (0.7%) with strong positivity Overall, 14 of 150 tumor categories showed detectable TH expression and only 5 tumor categories included at least one case with strong TH positivity. TH staining was most frequent in pheochromocytomas (100%, including 74.0% with strong positivity), ganglioneuroma (25.0%; including 16.7% with strong positivity), paragangliomas "probably sympathetic" (50.0%; including 43.8% with strong positivity), and paragangliomas "probably parasympathetic" (13.6%; of which all showed strong positivity). Other tumor types showing TH positivity less commonly and at a lower level included medullary thyroid carcinoma (5.9%), squamous cell carcinomas of several organs of origin (up to 4.5%), neuroendocrine neoplasms from several organs (up to 4.3%) and colorectal adenocarcinoma (0.2%). In "non-neural crest" derived tumors, TH staining was often limited to few interspersed cells. In conclusion, a strong positive TH immunostaining is highly specific for pheochromocytomas, ganglioneuroma, and paragangliomas although sensitivity is < 30% for paragangliomas.

Indexed as

Diagnostic aidImmunohistochemistryNormal tissue analysisPan-cancer analysisPathologyTissue microarrayTyrosine hydroxylase

Identifiers

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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 Socratic graph.