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A 23-year-old woman, gravida 1, para 1, was transferred to our hospital with acute lower abdominal pain and vital signs consistent with shock. Her urine concentration of human chorionic gonadotrophin was 8000 mIU/mL. Transvaginal ultrasound revealed an echo-free space with mosaic echo pattern in the right adnexal area and no gestational sac in the uterus. With a preoperative diagnosis of ruptured ectopic pregnancy, emergency laparotomy was performed. The rectouterine pouch was filled with many clots containing small amounts of villous tissue. After removal of the conceptus, which was infiltrating into the peritoneum of the Pouch of Douglas, bleeding was controlled by Argon laser. Histological examination of the conceptus by immunohistochemical staining with p57(kip2) showed features of complete hydatidiform mole. This case demonstrates that the peritoneum in the Pouch of Douglas is a possible site of ectopic complete hydatidiform mole occurrence and that immunohistochemical stain is useful to confirm the diagnosis of ectopic complete hydatidiform mole.
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http://dx.doi.org/10.1111/jog.12287 | DOI Listing |
Contraception
March 2025
Northwell, 2000 Marcus Ave, Suite 300, New Hyde Park, NY 11042; Zucker School of Medicine at Hofstra/Northwell, 500 Hofstra University, Hempstead, NY 11549. Electronic address:
This case report demonstrates hyperthyroidism complicating a twin gestation consisting of a complete hydatidiform mole and coexisting fetus. The patient underwent medical optimization of hyperthyroidism with a thionamide and beta blocker prior to undergoing uncomplicated dilation and evacuation under spinal anesthesia. She was cared for by a multidisciplinary team.
View Article and Find Full Text PDFMol Cytogenet
February 2025
Departments of Pathology and Laboratory Medicine, UT-Health San Antonio, 7703 Floyd Curl Drive, San Antonio, TX, 78229, USA.
Background: Gestational trophoblastic neoplasms consist of complete and partial hydatidiform moles, both of which are considered aberrant conceptuses. Both conditions, complete hydatidiform mole (CHM) and partial hydatidiform mole (PHM), differ in histological characteristics, genetic origin and content and clinical features. CHM have a diploid karyotype, mostly 46,XX but lack maternal genetic contribution with all chromosomes of paternal origin.
View Article and Find Full Text PDFObstet Gynecol Int
February 2025
Department of Obstetrics and Gynecology, Faculty of Medicine, Universidad Nacional de Colombia, Bogotá, Colombia.
To describe the incidence of hydatidiform mole in Colombia. Cross-sectional descriptive study. Colombia.
View Article and Find Full Text PDFAnn Pathol
January 2025
Service de pathologie, centre hospitalier Lyon Sud, 165, chemin du Grand-Revoyet, 69495 Pierre Bénite cedex, France. Electronic address:
Am J Surg Pathol
January 2025
Service de Pathologie Multi-Site, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon.
The distinction between choriocarcinoma and residual trophoblastic cell proliferation from a complete hydatidiform mole/invasive mole (CHM/IM) without villi is challenging on curettage materials. We investigated whether SALL4 immunostaining could help differentiate various gestational trophoblastic diseases. Placental site nodules (PSN; n=10), atypical PSN (APSN; n=8), placental site trophoblastic tumors (PSTT; n=9), epithelioid trophoblastic tumors (ETT; n=5), gestational choriocarcinomas (n=31), partial hydatidiform moles (PHM; n=13), CHM/IM (n=47), and nonmolar products of conception (POC) (n=26) were included.
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