Results 111 to 120 of about 16,149 (262)

Non‐trophoblastic tumours of the placenta: pathophysiology, diagnosis and management

open access: yesThe Obstetrician &Gynaecologist, Volume 27, Issue 2, Page 91-103, April 2025.
Key content Non‐trophoblastic tumours include chorioangiomas, teratomas, placental mesenchymal dysplasia (PMD), leiomyomas and more rarely hepatocellular adenomas. Ultrasonography is the primary diagnostic modality. Chorioangiomas are the most common benign non‐trophoblastic placental tumour, occurring within 1% of placentas microscopically.
Jack Le Vance   +4 more
wiley   +1 more source

A Cross-Sectional Analysis of the Incidence of Hydatidiform Mole in Colombia

open access: yesObstetrics and Gynecology International
Conclusions: The high proportion of unspecified hydatidiform mole far exceeds the diagnoses of complete and partial hydatidiform mole. The descriptive design of the study does not allow us to determine the causes of these results.
Mario Arturo González Mariño
doaj   +1 more source

Partial molar pregnancy with live fetus diagnosed on second trimester: a case report [PDF]

open access: yes, 2016
Hydatidiform mole is part of a group of diseases classified as gestational trophoblastic disease, which results from an aberrant fertilization. They are associated with an increase risk for the development of neoplasm, specifically choriocarcinoma, a ...
Cardoso, Rosete Maria Amorim Novais Nogueira   +4 more
core   +1 more source

Association of gestational trophoblastic disease with subsequent development of non‐trophoblastic cancer

open access: yesInternational Journal of Gynecology &Obstetrics, Volume 168, Issue 3, Page 1305-1311, March 2025.
Abstract Objective To evaluate the association between gestational trophoblastic disease and the subsequent risk of developing non‐trophoblastic cancer. Methods We conducted a retrospective cohort study of 3084 women with gestational trophoblastic disease and 1 415 812 women with obstetric deliveries in Quebec, Canada, between 1989 and 2021.
Blaise Munyakarama   +4 more
wiley   +1 more source

Features of radiodiagnosis of syndrome of pleural effusion [PDF]

open access: yes, 2016
The epidemic of tuberculosis, registered in Ukraine in 1995, remains a threat to society. Unfortunately, it cannot be overcomed, despite all the efforts.
Diedkova, Kateryna Andriivna   +6 more
core  

Trisomy 21 alters DNA methylation in parent-of-origin-dependent and independent manners [PDF]

open access: yes, 2016
The supernumerary chromosome 21 in Down syndrome differentially affects the methylation statuses at CpG dinucleotide sites and creates genome-wide transcriptional dysregulation of parental alleles, ultimately causing diverse pathologies.
Alves da Silva, Antônio Francisco   +12 more
core   +3 more sources

A Case report of atypical preeclampsia with severity criteria for hydatidiform complete mole. [PDF]

open access: gold, 2023
Orlando Rubén Pérez‐Nieto   +8 more
openalex   +3 more sources

Pemphigoid Gestationis after Spontaneous Expulsion of a Massive Complete Hydatidiform Mole

open access: yesCase Reports in Obstetrics and Gynecology, 2013
Pemphigoid gestationis (PG) is a rare, perinatal, autoimmune, and blistering dermatosis. Only few cases of PG involving hydatidiform moles have been reported. Complete hydatidiform moles are usually evacuated by dilatation and curettage.
Naoki Matsumoto   +8 more
doaj   +1 more source

Invasive mole: a rare cause of postmenopausal bleeding [PDF]

open access: yes, 2016
Gestational trophoblastic disease (GTD) describes a number of gynaecological tumours that originate in the trophoblast layer, including hydatidiform mole (complete or partial), placental site trophoblastic tumour, choriocarcinoma and invasive mole ...
Guèye, Mamour   +5 more
core   +1 more source

Does cerclage improve neonatal outcomes in a molar pregnancy and a coexistent fetus? a case report [PDF]

open access: yes, 2012
Background Complete hydatiform mole and coexistent viable fetus is very rare. The use of a cervical cerclage for cervical indications in the presence of this condition has never been reported.
Aguin, Eduardo   +5 more
core   +2 more sources

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