Results 41 to 50 of about 4,020 (177)
A Rare Case of Disseminated Peritoneal Leiomyomatosis: A Case Report
Disseminated peritoneal leiomyomatosis is a benign condition characterized by multiple extrauterine leiomyomas in various locations such as the peritoneum, mesentery, abdominal wall, and pelvis.
Michael Chirayath +3 more
doaj +1 more source
Background Intravenous leiomyomatosis is characterized by the extension of pathologically benign smooth muscle tumor into venous channels. Its extension into the heart is a very rare occurrence, which may lead to heart failure and occasionally sudden ...
Rohit Bhoil +6 more
doaj +1 more source
The WHO Classification of Genetic Tumour Syndromes: Considerations for Genetics
The WHO Classification of Tumours underpins the diagnosis of neoplastic conditions. The new WHO classification of genetic tumour syndromes (GTS) provides international standards for their diagnosis. This diagram highlights the chromosomal distribution of the genes involved in the GTS covered in this classification.
Ian A. Cree +18 more
wiley +1 more source
Molecular and Genetic Landscape of Intravenous Leiomyomatosis: A Narrative Review
Intravenous leiomyomatosis is a rare uterine benign tumor characterized by intravascular growth, quasi‑malignant behavior, and a high recurrence rate. This review summarizes its molecular and genetic research progress, compares it with similar tumors, discusses unsolved issues and prospects, contributing to its pathogenesis, diagnosis, and future ...
Lei Li +7 more
wiley +1 more source
Hereditary leiomyomatosis and renal cell cancer syndrome associated renal cell carcinoma
Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) is a recently described entity with unknown exact prevalence. The affected individuals are predisposed to have multiple leiomyomas and renal cancer due to germline mutation in fumarate hydratase ...
Shraddha Adamane +2 more
doaj +1 more source
Hereditary Leiomyomatosis and Renal Cell Cancer
Hereditary leiomyomatosis and renal cell cancer is a genodermatosis with an autosomal dominant inheritance pattern. It is a tumour predisposition syndrome characterized by cutaneous and uterine leiomyomas, and increased susceptibility to develop renal ...
Anders Würgler Hansen +4 more
doaj +1 more source
ABSTRACT Background and Aims Cancer cells undergo adaptation in hostile tumor microenvironments and go through extensive metabolic reprogramming for flourishing. Oncogenic transformation caused by mutations in some metabolic enzymes results in the generation of some metabolic intermediates called onco‐metabolites.
Mst. Mohona Khatun +8 more
wiley +1 more source
Primary peritoneal tumours are uncommon and include mesothelioma and carcinoma. Mesothelioma identification is challenging, as there are no established rapid diagnostic methods. In the absence of a simple means of diagnosis, evaluation often requires several invasive biopsies, highlighting the need to develop a definitive diagnostic method.
T Tanaka, M Tomihari, T Hasegawa
wiley +1 more source
ABSTRACT Objective To identify the risk factors associated with postoperative recurrence of unusual (special‐type) uterine smooth muscle neoplasia (USMN) and to construct and interpret a machine‐learning model for recurrence risk. Methods We carried out a retrospective review of patients who had myomectomy for uterine masses at the Third Xiangya ...
Weiwei Hu +5 more
wiley +1 more source
Case report: Uterine leiomyoma with fumarate hydratase deficiency
Hereditary leiomyomatosis and renal cell cancer syndrome is a rare autosomal dominant disease caused by mutations in the fumarate hydratase gene. The syndrome is characterized by skin leiomyomatosis, uterine leiomyomatosis, and renal cell carcinoma ...
Diana Bužinskienė +5 more
doaj +1 more source

