ArticleThe American journal of case reports2025
Diagnosing Disseminated Peritoneal Leiomyomatosis: Malignancy-Like Presentation in a 59-Year-Old Woman.
Article in The American journal of case reports, 2025. 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
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
BACKGROUND Disseminated peritoneal leiomyomatosis (DPL), or leiomyomatosis peritoneal disseminata, is a benign condition that presents with multiple lower abdominal peritoneal nodules consisting of smooth muscle cells, which can slowly increase in size. The risk of malignant transformation is 2% to 5%. The mechanisms underlying the pathogenesis and malignancy of DPL are unclear and can be associated with a variety of factors. This report describes a 59-year-old woman presenting with multiple abdominal masses and a diagnosis of DPL. CASE REPORT This report describes a 59-year-old female patient who experienced abdominal pain and difficulty defecating. Proctoscopy showed intestinal stenosis and inflammatory changes. She may have had renal dysfunction. The medical history showed that the patient had uterine fibroids in the past and had undergone hysterectomy surgery. We cannot confirm whether the patient received hormone therapy before admission. Based on the results of histopathology and immunohistochemistry, it was considered to be a DPL. The patient died 6 months after surgery. CONCLUSIONS DPL is a rare disease that is difficult to diagnose and traditionally considered a benign condition. This report emphasizes the importance of understanding the presentation and distribution of DPL, as it can mimic the deposition of malignant tumors. This case also emphasizes the importance of diagnosing benign tumors through histopathology. The mechanism of malignant transformation of DPL is currently unclear, and it is of great significance to combine multiple detection methods in clinical practice to determine its malignancy.
Indexed as
Identifiers
What Socratic 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 Socratic graph.