Results 91 to 100 of about 359,174 (252)
Diagnosis and surgical therapy of uterine sarkoma
Introduction: Uterine sarcomas are rare gynaecological neoplasms and their classification is complicated. Uterine sarcoma is usually diagnosed in postmenopausal women and the diagnosis is often accidental and postoperative.
R. Argirovic, N. Ladjevic N
core
The graphical abstract illustrates the interconnected relationship between food safety management, mycotoxin toxicity, and detoxification strategies, highlighting how preventive measures across the food chain can minimize mycotoxin contamination and reduce adverse health effects in humans/animals.
Chinaza Godswill Awuchi
wiley +1 more source
ABSTRACT Background Leiomysosarcoma (LMS) is generally associated with high metastatic potential and poor survival. Cutaneous LMS (cLMS) has been considered a different entity with more indolent biological behavior. Methods A narrative review was performed to assess the biological behavior of cLMS, with special attention for the head and neck location.
Eelco de Bree +8 more
wiley +1 more source
Survival analysis of patients with rare tumors of the uterine corpus – carcinosarcoma [PDF]
Background/Aim. Uterine carcinosarcoma (UCS), formerly known as malignant mixed Müllerian tumor, is a rare, aggressive malignancy of the female genital tract.
Stevanović Nemanja +7 more
doaj +1 more source
Malignant Uterine Neoplasms Attended at a Brazilian Regional Hospital: 16-years Profile and Time Elapsed for Diagnosis and Treatment. [PDF]
Candido EC +5 more
europepmc +1 more source
Abstract Lynch syndrome (LS) is the most common hereditary colorectal cancer syndrome, caused by a germline pathogenic variant in one of the mismatch repair (MMR) genes. Among these, MSH6‐associated LS represents a distinct subtype with unique molecular and clinical characteristics.
Salwa Ben Yahia +4 more
wiley +1 more source
Epithelioid trophoblastic tumor
Objective: To describe a case of epithelioid trophoblastic tumor (ETT) in a postmenopausal woman, which had several peculiar features that differentiate it from previously reported ETTs.
Sevinc Hallac Keser +5 more
doaj +1 more source
ABSTRACT Approximately 6%–8% of children and adolescents with rhabdomyosarcoma (RMS) have an underlying cancer predisposition disorder (CPD), which varies between embryonal and alveolar subtypes and other clinical characteristics. Identifying a CPD remains challenging, as traditional approaches rely on clinical features and family history. Additionally,
Taylor M. Luckie +12 more
wiley +1 more source
A Giant Subserosal Uterine Leiomyoma Mimicking an Abdominal Mass: Multimodal Imaging Data
Giant uterine leiomyomas are extremely rare neoplasms and are challenging both diagnostically and therapeutically. A 49-year-old premenopausal female presented at our Department complaining of abdominal pain and distention for several years.
Tugce Ozlem Kalayci +3 more
doaj
Uterine lipoleiomyoma: rare presentation of postmenopausal bleeding [PDF]
Uterine lipoleiomyomas are rare benign tumors composed of mature adipose tissue and smooth muscle cells. They account for less than 0.2% of all uterine neoplasms and are typically asymptomatic, often discovered incidentally.
Sahay, Vinita, Sahay, Nehal
core +1 more source

