A case of fetal axillary hemangiolymphangioma coexisting with intralesional hemorrhage is presented. At 27 weeks' gestation, the fetus was found to have a 52 x 43-mm left axillary multilocular cystic mass which showed no signals on color Doppler. The mass was composed mostly of sonolucent spaces. At 29 weeks' gestation, an arterial flow signal (15 cm/s) was detected within the mass. In addition, two low-density echogenic cystic spaces with bidirectional flow waveforms were found, which raised the suspicion of intratumoral bleeding. Two weeks later, a fine-needle aspiration of the mass revealed both straw-colored and chocolate-colored fluid. The tumor size increased from 52 x 43 mm at 27 weeks to 100 x 79 mm at 37 weeks. Blood clots developed gradually in the hemorrhagic spaces. The pregnancy proceeded smoothly to term and at 38 weeks an elective Cesarean section was performed. After a surgical excision of the mass at the age of 4 days, a mixed cavernous hemangioma and cystic lymphangioma with secondary intralesional hemorrhage was confirmed histopathologically.
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http://dx.doi.org/10.1046/j.1469-0705.2002.00633.x | DOI Listing |
Cureus
October 2024
Obstetrics and Gynaecology, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.
Darier disease (DD), which was also known as keratosis follicularis or Darier-White disease, is an autosomal dominant hereditary illness. The illness typically first manifests in adolescence and progresses as a woman reaches reproductive age. Research on the potential effects of DD on the skin and fetus, especially when it affects the groin and vulva, is insufficient.
View Article and Find Full Text PDFRadiol Case Rep
January 2025
Department of Obstetrics and Gynecology, Dilla University, College of Medicine and Health Sciences, Dilla, Ethiopia.
Cystic hygroma is a congenital lymphatic malformation characterized by fluid-filled cysts, often located in the neck or axillary regions, and is associated with significant fetal morbidity and mortality. This case report details a 32-year-old gravida 7 para 6 at 15 weeks of gestation, diagnosed prenatally with a large cystic hygroma exhibiting septation in the cervicoccipital and axillary region, accompanied by bilateral pleural effusion, pericardial effusion and subcutaneous edema. This report underscores the importance of early diagnosis and the need to carefully consider management options in cases of cystic hygroma with fetal hydrops.
View Article and Find Full Text PDFLancet Microbe
October 2024
South Africa Medical Research Council Vaccines and Infectious Diseases Analytics Research Unit, Faculty of Health Science, University of the Witwatersrand, Johannesburg, South Africa; African Leadership in Vaccinology Expertise, Faculty of Health Science, University of the Witwatersrand, Johannesburg, South Africa; Wits Infectious Diseases and Oncology Research Institute, Faculty of Health Science, University of the Witwatersrand, Johannesburg, South Africa. Electronic address:
Eur Radiol
July 2024
Department of Radiology and Nuclear Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
JBMR Plus
August 2024
Division of Endocrinology, Diabetes and Metabolism, Indiana University School of Medicine, Indianapolis, IN 46202, United States.
Maternal Parathyroid Hormone-related Protein (PTHrP) is involved in the placental transport of calcium. Autonomous overproduction of PTHrP is a rare cause of hypercalcemia in pregnancy. Prior cases of PTHrP-induced hypercalcemia in pregnancy have been managed with either dopamine agonists, fetal delivery, termination of pregnancy, or mastectomy.
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