Results 41 to 50 of about 6,280 (170)
Uterine adenosarcoma (UA) is an uncommon mixed tumor containing a benign to at most mildly atypical epithelial component and a sarcoma‐like stroma, usually a low‐grade, stromal component, with rare heterogeneous elements. Currently, tumor etiology is largely unknown.
Yao Li +6 more
wiley +1 more source
Persistent Müllerian Duct Syndrome: Understanding the Challenges
Persistent Müllerian duct syndrome (PMDS) is a rare autosomal recessive condition defined by the presence of Müllerian duct‐derived structures in an otherwise normally masculinized phenotypical and genotypical (46,XY) male. We describe the case of an infant diagnosed with PMDS, managed and followed up for 7 years.
Irene Chua, Naeem Samnakay, Walid Farhat
wiley +1 more source
Hypercalcaemia and its systemic sequelae are a relatively common finding amongst patients in the field of endocrinology. Primary hyperparathyroidism, a frequent cause of hypercalcaemia, is often seen among middle‐aged female patients, typically resulting from an underlying single‐gland adenoma.
Maxim Barnett +5 more
wiley +1 more source
An Exceptional Occurrence of Uterus Mullerian Adenosarcoma in a Young Iranian Woman
Uterus mullerian adenosarcoma is a very rare malignancy. The clinical and Ultra Sonographic findings are not exclusive and the histomorphologic diagnosis of low-grade adenosarcomas is not straightforward.
Samiee-Rad, Fatemeh
core +1 more source
Mullerian adenosarcoma is a rare biphasic malignant neoplasm of cervix characterized by an admixture of benign epithelial elements and a malignant sarcomatous stromal component, which may be either homologous or heterologous.
Debahuti Mohapatra +2 more
doaj +1 more source
Extragenital Müllerian adenosarcoma with pouch of Douglas location
Background Of all female genital tract tumors, 1-3% are stromal malignancies. In 8-10% of cases, these are represented by Müllerian adenosarcoma an extremely rare tumor characterized by a stromal component of usually low-grade malignancy and by a benign ...
Thai Elena +8 more
doaj +1 more source
Abstract Individuals with DICER1 syndrome, a genetic disorder caused by pathogenic germline variants in DICER1, are at increased risk of developing a wide array of predominantly childhood onset conditions, including genitourinary sarcomas. However, data on DICER1 involvement in paratesticular sarcomas have not been published.
Maria Apellaniz‐Ruiz +7 more
wiley +1 more source
Endometrial stromal sarcomas with BCOR‐rearrangement harbor MDM2 amplifications
Abstract Recently a novel subtype of endometrial stromal sarcoma (ESS) defined by recurrent genomic alterations involving BCOR has been described (HGESS‐BCOR). We identified a case of HGESS‐BCOR with a ZC3H7B‐BCOR gene fusion, which harbored an amplification of the MDM2 locus.
Felix KF Kommoss +15 more
wiley +1 more source
Ovarian adenosarcoma simulating a simple cyst in a young patient
Müllerian adenosarcoma is a rare, mixed tumor that can occur throughout the female genital tract, but is most commonly found in the uterus. Ovarian adenosarcoma is rarer and has a poorer prognosis than uterine adenosarcoma.
Leonardo Gomes da Fonseca +5 more
doaj +1 more source
A rare case of extragenital Müllerian adenosarcoma
A 51-year-old gravida 5 para 5 (5005) presented with an increasing abdominal girth and a palpable abdominal mass. She was initially diagnosed with ovarian new growth and underwent exploratory laparotomy. Intraoperatively, the uterus, Fallopian tubes, and
Pauline Beatriz S. Gonzaga +1 more
doaj +1 more source

