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1.
Minerva Ginecol ; 56(2): 155-9, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15258545

ABSTRACT

Haemoglobin E is a beta chain variant quite common in Southeastern Asia. The case of a gravid Thai woman with a microcytic anaemia is reported. The diagnosis of homozygous haemoglobin E was suspected on the basis of ethnic considerations when analysis of her haemoglobin showed the absence of normal HbA1 and about 100% of a variant Hb with electrophoretic mobility with HbC and HbA2. Identification of the haemoglobin variant was performed by using an association of alkaline electrophoresis on agarose gel, acid electrophoresis on agarose gel, haemoglobin isoelectrofocusing, high performance liquid chromatography. A study of haemoglobin pattern in the partner, parents and siblings was also performed. Pregnancy continued without any problems until the 40th week when a caesarean section was performed due to a difficult labour with foetal distress. The haemoglobin pattern of the new-born was studied at birth and after 1 year; as expected, it was quite normal at birth and a heterozygous condition for HbE was observed after 1 year. HbE, in even heterozygous and homozygous states, gives a mild clinical picture but its association with other haemoglobinopathies, such as a double heterozygous state (i.e. HbE/beta Thalassaemia) gives rise to a severe transfusion dependent thalassaemia syndrome. It is the authors' opinion that only a strict interaction between obstetricians and pathologists is the possible correct answer to the new diagnostic question proposed by a rapidly evolving inter-ethnic society.


Subject(s)
Hemoglobin E/genetics , Pregnancy Complications, Hematologic , Adult , Female , Follow-Up Studies , Genetic Counseling , Humans , Infant, Newborn , Male , Pedigree , Pregnancy , Pregnancy Complications, Hematologic/diagnosis
2.
Clin Exp Rheumatol ; 16(5): 605-10, 1998.
Article in English | MEDLINE | ID: mdl-9779312

ABSTRACT

OBJECTIVE: The outcome of 55 infants born to 53 antiphospholipid antibody (aPL)-positive mothers treated during pregnancy with calcium heparin is described. METHODS: The clinical state of the children was evaluated immediately after delivery by a clinical examination, and a neonatological check-up was performed no later than 24 hours after birth. Neonates with problems were transferred to the neonatal intensive care unit. After their discharge from hospital the clinical state of the babies was followed by means of interviews with the pediatricians and mothers for a period varying between 1.33 and 5.66 years (mean 2.51 +/- 0.92 SD). RESULTS: The newborns comprised 30 females and 25 males, including 2 sets of twins, delivered between the 25th and 40th weeks of gestation (mean 36.69 +/- 2.91 SD). They had a mean birth weight of 2.828 g +/- 706.50 SD (range 800-4.000) and a mean Apgar score at 5 minutes of 9.60 +/- 0.68 SD (range 7-10). Soon after delivery, 12 children (21.81%) were admitted to the neonatal intensive care unit for periods varying between 2 and 120 days (mean 30.33 +/- 33.40 SD), after which the clinical course was normal. All of these neonates suffered from complications exclusively due to prematurity. Malformations and signs of thrombosis or other aPL-related disorders were not observed in any of the newborns. During the follow-up, none of the diseases suffered by the 55 children differed from those of the normal pediatric population; in particular, aPL-related manifestations were never observed. CONCLUSION: These data indicate the absence of aPL-related problems in the offspring of aPL-positive mothers treated during pregnancy with calcium heparin.


Subject(s)
Antibodies, Antiphospholipid/analysis , Antiphospholipid Syndrome/drug therapy , Fibrinolytic Agents/therapeutic use , Heparin/therapeutic use , Pregnancy Complications/drug therapy , Pregnancy Outcome , Adult , Antiphospholipid Syndrome/immunology , Female , Humans , Infant, Newborn , Male , Pregnancy , Pregnancy Complications/immunology , Treatment Outcome
3.
Clin Exp Obstet Gynecol ; 22(2): 165-8, 1995.
Article in English | MEDLINE | ID: mdl-7781185

ABSTRACT

Literature data indicate that rupture of arterovenous malformations is 4 times more frequent in pregnant women. The Authors present a case of cerebral hemangioma of the third medium anterior of the corpus callosum diagnosed in a patient at the 28th gestational week by Magnetic Resonance scan. The patient underwent elective caesarean section under peripheral anesthesia (peridural and spinal block by Bupivacaine) and delivered a male infant 4560 gr, 52 cm. The postoperative course was uneventful. The arterovenous malformation constituted an important anesthesiologic risk factor but the Authors conclude that caesarean section can be safely performed with a very careful anesthesiological time schedule and a reliable haemodynamic monitoring.


Subject(s)
Brain Neoplasms/complications , Corpus Callosum , Hemangioma/complications , Pregnancy Complications, Neoplastic , Pregnancy, High-Risk , Adult , Brain Neoplasms/surgery , Cesarean Section , Female , Hemangioma/surgery , Humans , Pregnancy , Pregnancy Complications, Neoplastic/surgery , Radiosurgery
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