Objective: To present intensive intrauterine treatment of recurrent early onset fetal erythroblastosis due to anti-M alloimmunization. Case Report: A 33-year-old woman, gravid 3, para 1, had anti-M IgG antibody, which caused alloimmunization of her ...
Tzu-Hung Lin+5 more
doaj +2 more sources
ERYTHROBLASTOSIS AND FETAL GROWTH RETARDATION (IUGR) [PDF]
Pediatric Research, 1987Top of pageAbstract Little has been published about circulating nucleated red blood cells (NRBC) in very low birth weight (VLBW) infants. We saw marked erythroblastosis (increased NRBC) in several infants with severe IUGR who were also VLBW. Hence, we evaluated the NRBC of all VLBW infants admitted to our intensive care nursery in 1983-86.
A M Tito, Alistair G.S. Philip
openaire +3 more sources
Non-RhD alloimmunization in pregnancy: an updated review [PDF]
Revista Brasileira de Ginecologia e ObstetríciaRhD alloimmunization in pregnancy is still the main cause of hemolytic disease of the fetus and neonate (HDFN). Nevertheless, there are other antigens that may be associated with the occurrence of this phenomenon and that have been growing in proportion,
Sabrina Menes Ares+3 more
doaj +2 more sources
Maternal mirror syndrome with foetal hydrops due to isoimunization by anti-KPa antibodies: A case report and narrative literature review. [PDF]
Clin Case Rep, 2022The association of fetal hydrops with maternal edema should prompt the suspicion of mirror syndrome. In the consideration of fetal hydrops, it is important to include immunohematological studies that rule out the presence of rare antibodies. Abstract We present a rare case of mirror syndrome due to anti‐Kpa antibodies, which can be difficult to ...
Pina Moreno J+3 more
europepmc +2 more sources
An intriguing case of a paravertebral extramedullary erythropoiesis presenting as tumor-mimicking lesion in a patient with eosinophilia with FIP1L1-PDGFRA rearrangement. [PDF]
Clin Case Rep, 2022This is the first reported case of extramedullary hematopoiesis interesting only one cell lineage (erythrocytes) presenting as an isolated tumor‐like lesion in the posterior mediastinum in a 28‐year‐old man with a 13‐year history of eosinophilia with FIP1L1‐PDGFRA fusion gene successfully surgically treated. Abstract Extramedullary hematopoiesis in the
Farah S+6 more
europepmc +2 more sources
Hemolytic Disease of the Newborn: A Review of Current Trends and Prospects [PDF]
Pediatric Health, Medicine and Therapeutics, 2021Akshay Kiran Myle,1,2 Ghanim Hamid Al-Khattabi2 1Department of Clinical Research, General Medicine, Pharmacology, Integrative Medicine, Clinical Researcher.
Myle AK, Al-Khattabi GH
doaj +2 more sources
A closer look at discordant placental echogenicity: two cases under the microscope. [PDF]
Clin Case Rep, 2021Discordant placental echogenicity is observed in MC pregnancies complicated with twin anemia‐polycythemia sequence, but could also belong to complicated singleton gestation. Abstract Discordant placental echogenicity is observed in MC pregnancies complicated with twin anemia‐polycythemia sequence, but could also belong to complicated singleton ...
Lanna MM+6 more
europepmc +2 more sources
Prevalence of erythrocyte alloimmunization in polytransfused patients [PDF]
Einstein (São Paulo), 2011Objective: To determine the incidence and the rate of red blood cellalloimmunization in polytransfused patients. Methods: A polytransfusedpatient was defined as having received at least 6 units of red cellconcentrates during a 3-month period. The records
Roberto de Oliveira Cruz+6 more
doaj +4 more sources
Yolk sac development, function and role in rodent pregnancy
Birth Defects Research, Volume 115, Issue 14, Page 1243-1254, August 15, 2023., 2023Abstract During the early phases of embryonic development, the yolk sac serves as an initial placenta in many animal species. While in some, this role subsides around the end of active organogenesis, it continues to have important functions in rodents, alongside the chorio‐allantoic placenta.
Asher Ornoy, Richard K. Miller
wiley +1 more source
Symphony in the crowd: Key genetic alterations in prostate cancer
Cancer Innovation, Volume 2, Issue 3, Page 203-209, June 2023., 2023Genetic alterations in prostate cancer (PCa). PCa progresses from a recurrent inflammation of the prostatic epithelia to an aggressive form. The key genetic alterations during this conversion include: altered androgen receptor (AR), gene fusion, alteration of tumor suppressors, defective DNA repair mechanism.
Neshat Masud
wiley +1 more source