ArticleIranian journal of pathology2026
Uncovering the Pleomorphic Hyalinizing Angiectatic Tumor: A Case Series and Literature Review.
Article in Iranian 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
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background & Objective: Pleomorphic hyalinizing angiectatic tumor (PHAT) is a rare fibrohistiocytic neoplasm, classified by the World Health Organization (WHO) as a "neoplasm of uncertain behavior of connective or soft tissue" within the soft tissue and bone tumor group. A literature review via Scopus and PubMed revealed approximately 133 reported cases worldwide, affecting individuals aged 10 to 86 years, with a slight female predominance and wide anatomical distribution. Case Presentation: We report a series of 4 PHAT cases, the first from India and the fourth largest globally. The cases include a 37-year-old male with a large upper abdominal wall mass, a 46-year-old male with a forearm swelling, a 36-year-old female with a lower leg mass, and a 40-year-old male with a lower abdominal mass. Histopathology showed characteristic features, including ectatic vessels, hyalinization, and pleomorphic spindle cells. Conclusion: Given its rarity and histologic overlap with other tumors, increased awareness and accurate histopathological diagnosis of PHAT are essential.
Indexed as
Identifiers
What 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.