ReviewVirchows Archiv : an international journal of pathology2026
Sweat gland carcinoma: a comprehensive review Part I: sweat gland carcinomas arising de novo.
Review 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.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Sweat gland carcinomas constitute a heterogeneous group of malignant neoplasms with differentiation towards the sweat gland apparatus that may arise de novo or from the transformation of a precursor. Over the last few years, a number of specific genetic alterations have been identified allowing a more accurate classification of this diverse group of neoplasms. In the present review, we focus on adnexal sweat gland carcinomas arising de novo including microcystic adnexal carcinoma, squamoid ductal eccrine carcinoma (SDEC), Endocrine mucin-producing sweat gland carcinoma and mucinous carcinoma, digital papillary adenocarcinoma, adenoid cystic carcinoma, apocrine carcinoma, secretory and microsecretory carcinoma and NUT adnexal carcinoma. The main clinical, morphological, immunohistochemical and molecular features of these tumour entities are described and the main differential diagnoses are discussed.
Indexed as
Identifiers
42217005What OpenQuestion holds
Registered trials
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.