Rectal leiomyosarcoma as the initial phenotypic manifestation of Li-Fraumeni-like syndrome: a case report and review of the literature

Leiomyosarcoma is a rare malignant tumor of smooth muscle origin and represents 10-20% of all soft tissue sarcomas. Primary colon and rectal sarcomas constitute

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Journal of medical case reports 2022-12, Vol.16 (1), p.468-7, Article 468
Hauptverfasser:	Severino, Natalia Parisi, Waisberg, Jaques, Fragoso, Maria Candida Barisson Villares, de Lima, Luiz Guilherme Cernaglia Aureliano, Balsamo, Flavia, Henriques, Alexandre Cruz, Bianco, Bianca, de Sousa Gehrke, Flávia
Format:	Artikel
Sprache:	eng
Schlagworte:	Abdomen Adrenal Cortex Neoplasms - complications Adrenal Cortex Neoplasms - genetics Adrenocortical Carcinoma Aged Analysis Antigens Biopsy Breast cancer Cancer therapies Case Report Case reports Chemotherapy Child Colonoscopy Colorectal cancer DNA sequencing Female Genetic aspects Genetic polymorphisms Genetic Predisposition to Disease Humans Leiomyosarcoma Leiomyosarcoma - diagnosis Leiomyosarcoma - genetics Leiomyosarcoma - surgery Li-Fraumeni Syndrome - complications Li-Fraumeni Syndrome - diagnosis Li-Fraumeni Syndrome - genetics Liver Li–Fraumeni syndrome Male Metastasis Mutation Neuroendocrine tumors Nucleotide sequencing Ostomy Pelvic Neoplasms Pelvis Prostate cancer Rectal Neoplasms - diagnosis Rectal Neoplasms - genetics Rectal Neoplasms - surgery Rectum Sarcoma Smooth muscle Surgical anastomosis TP53 gene Tumor proteins Tumor Suppressor Protein p53 - genetics Tumors Uterus
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Beschreibung
Zusammenfassung:	Leiomyosarcoma is a rare malignant tumor of smooth muscle origin and represents 10-20% of all soft tissue sarcomas. Primary colon and rectal sarcomas constitute
ISSN:	1752-1947 1752-1947
DOI:	10.1186/s13256-022-03671-6