Results 51 to 60 of about 5,364 (214)

Whole‐genome paternal uniparental disomy identified through prenatal single‐nucleotide polymorphism‐based cell‐free DNA screening

Ultrasound in Obstetrics &Gynecology, Volume 67, Issue 1, Page 73-78, January 2026.
ABSTRACT Objective Prenatal single‐nucleotide polymorphism (SNP)‐based cell‐free DNA (cfDNA) screening can identify genome‐wide paternal uniparental disomy (GW‐UPDpat), including cases with complete hydatidiform mole with a coexisting fetus (CHMCF), those with placental mesenchymal dysplasia (PMD) and those with a mosaic/chimeric GW‐UPDpat syndrome ...
P. Benn, K. Hashimoto, V. Souter, R. Dhamankar, W. Xu, D. Kijacic   +5 more
wiley   +1 more source

Abdominal Hysterectomy Under Thoracic Epidural Anesthesia for Complete Molar Pregnancy in a Patient With Atypical Preeclampsia and Hyperthyroidism in a Resource‐Limited Setting: Case Report and Literature Review

Case Reports in Anesthesiology, Volume 2026, Issue 1, 2026.
Background Hydatidiform mole is a rare gynecological disease arising from trophoblastic tissue. There is no standard anesthetic management for patients undergoing major abdominal surgery; the decision may be based on preoperative patient status, the presence of coexisting illnesses, the risk of aspiration, and the availability of advanced equipment ...
Mesay Milkias, Semagn Mekonnen, Fikru Milkiyas, Mebratu Kebede, Nigatu Tilahun, Srijoni Sengupta   +5 more
wiley   +1 more source

Characterization of apoptosis and autophagy through Bcl-2 and Beclin-1 immunoexpression in gestational trophoblastic disease

Iranian Journal of Reproductive Medicine, 2015
Background: The pathogenesis of Gestational Trophoblastic Disease (GTD) is not clearly known. Objective: In this study, immunoexpression of proteins Bcl-2 and Beclin-1 in trophoblastic lesions and normal trophoblastic tissue was conducted to study the ...
Teresa Liliana Wargasetia, Nurhalim Shahib, Djamhoer Martaadisoebrata, Diah Dhianawaty, Bethy Hernowo   +4 more
doaj  

Prevalence and Factors Associated with Hydatidiform Mole among Patients Undergoing Uterine Evacuation at Mbarara Regional Referral Hospital

Obstetrics and Gynecology International, 2018
Objective. We sought to determine the prevalence of and factors associated with hydatidiform molar gestations amongst patients undergoing uterine evacuation at Mbarara Regional Referral Hospital (MRRH), Mbarara, Uganda. Methods.
Olivier Mulisya, Drucilla J. Roberts, Elizabeth S. Sengupta, Elly Agaba, Damaris Laffita, Tusabe Tobias, Derrick Paul Mpiima, Lugobe Henry, Ssemujju Augustine, Masinda Abraham, Twizerimana Hillary, Julius Mugisha   +11 more
doaj   +1 more source

CASE OF HYDATIDIFORM MOLE. [PDF]

Journal of the American Medical Association, 1887
Dear Sir: —In the issue ofThe Journalof November 26, Dr. Thos. C. Smith, of Washington, D. C., reports two cases of "Hydatidiform Mole." As I also met with a case a short time since, and in many respects similar to the last of his cases, I beg to submit it to the profession. Mrs. W., aet. 41, white, has had six children. Previous history.
openaire   +2 more sources

Choriocarcinoma in the Cervix: Case Report of a Challenging Differential Diagnosis

Case Reports in Obstetrics and Gynecology, Volume 2026, Issue 1, 2026.
Background Primary cervical choriocarcinoma in abortion curettage tissue is extremely rare and represents a diagnostic challenge. It is a serious condition that requires prompt and targeted therapeutic management. This case report describes the diagnostic evaluation, taking into account relevant differential diagnoses and highlighting the importance of
Kristin Pfister, Rok Satler, Dieter Erdin, Andreas Müller, Gesine Meili, Peter Bode, Gabriel Levin   +6 more
wiley   +1 more source

A twin pregnancy with a hydatidiform mole and a coexisting live fetus: prenatal diagnosis, treatment, and follow-up

, 2017
Twin molar pregnancy with a hydatidiform mole and a coexisting live fetus is a rare form of gestational trophoblastic disease associated with an increased risk of obstetric complications and poor perinatal outcome.
Joffre Amim Júnior, Bruna Obeica, Sun, Sue Yazaki, Araujo Junior, Edward [UNIFESP], Júnior, Edward Araujo, Rezende Filho, Jorge, Antonio Braga, Edward Araujo Júnior, Júnior, Joffre Amim, Sue Yazaki Sun, Amim Junior, Joffre, Jorge Rezende Filho, Werner, Heron, Filho, Jorge Rezende, Heron Werner, Obeica, Bruna, Sun, Sue Yazaki [UNIFESP], Braga, Antonio   +17 more
core   +1 more source

Uterine Rupture on Invasive Molar Pregnancy Revealing a Choriocarcinoma: Case Report from a Low‐Income Country

Case Reports in Obstetrics and Gynecology, Volume 2026, Issue 1, 2026.
Introduction Gestational trophoblastic diseases are rare entities encompassing a wide spectrum of benign and malignant placental pathologies. Uterine rupture is primarily related to a uterine scar and, exceptionally, following an invasive mole or gestational choriocarcinoma.
Rakotomalala Nivoarimelina Zoly, Refeno Valéry, Ramarokoto Malalafinaritra Patrick Marco, Randaoharison Pierana Gabriel, Rafaramino Florine, Karuna Sharma   +5 more
wiley   +1 more source

Molecular cytogenetic analysis of a hydatidiform mole with coexistent fetus: a case report

Journal of Medical Case Reports, 2019
Background A hydatidiform mole with a coexisting fetus is a rare condition that commonly occurs as either a partial mole with fetus or a twin pregnancy comprising a complete mole and normal fetus.
Nozomi Uemura, Yasushi Takai, Yukiko Mikami, Miwa Ogasawara, Masahiro Saitoh, Kazunori Baba, Junichi Tamaru, Masaaki Hara, Hiroyuki Seki   +8 more
doaj   +1 more source

An Uncommon Presentation of Spontaneous Ovarian Hyperstimulation Syndrome in Pregnancy Complicated by Primary Hypothyroidism: A Case Report

Case Reports in Obstetrics and Gynecology, Volume 2026, Issue 1, 2026.
Spontaneous ovarian hyperstimulation syndrome (OHSS) is an extremely rare condition that occurs in pregnant women without the use of ovulation induction therapy. If not diagnosed early and treated promptly, it can lead to significant morbidity and mortality. Few cases of spontaneous OHSS have been reported in the published literature.
Celina R. Andonie, Saja I. AbuGhannam, Ina Khamashta, Manvinder Singh   +3 more
wiley   +1 more source