Intermittent hepatic porphyria in pregnancy with good perinatal outcome.

Porphyrias are rare metabolic diseases caused by enzymatic defects of the haeme biosynthesis. Association of pregnancy and acute porphyria is rare, but mortality rate among pregnant women from acute attack has been reported up to 42%. This paper presents a patient with pregnancy complicated by intermittent hepatic porphyria with good perinatal outcome. The pattern of the attack in pregnancy varies individually and it makes porphyric pregnancies a challenge. Previously diagnosed porphyria patients should be closely monitored during pregnancy and diagnosis of acute porphyria must be also considered in all pregnant women with unexplained abdominal pain.

Surgical treatment of large smooth muscle tumor of uncertain malignant potential during pregnancy.

This paper presents a case of a 37-year old pregnant woman with a large tumor extending from pelvis to xyphoid, diagnosed at 14 weeks of pregnancy. At 18 weeks myomectomy was performed and the tumor weighing 4250 g was removed. Hystopathological findings showed a uterine smooth muscle tumour of uncertain malignant potential. Due to preeclampsia an urgent caesarean section was performed at 34 weeks of gestational age. A live and healthy female neonate was delivered. According to hystopathological findings and in agreement with the patient hysterectomy without adnexectomy was performed in the same act.

A case of intra-amniotic maternal hemorrhage in term pregnancy.

INTRODUCTION: Intra-amniotic maternal hemorrhage is a rare condition, hard to differentiate from some other conditions in pregnancy. We report an unusual case of intra-amniotic maternal hemorrhage in term pregnancy ending in urgent cesarean section, identified on ultrasound examination. CASE REPORT: A 24-year-old female (gravida 3, para 2, abortion 0) was admitted to hospital at 40 weeks' gestation for collapse and general weakness. Her blood pressure was 90/60 mm Hg, pulse 112 bpm, temperature 36 degrees C. The fetal heart race tracings were stable and reactive. The cervix was opened 3 cm. Further examination revealed no vaginal bleeding and normal amnioscopic findings. An ultrasound examination confirmed singleton, head-presenting gestation without any visible congenital anomalies, amniotic fluid index was at the 50th percentile, anterior placenta without evidence of previa, abruption or retroplacental hematoma. An inhomogeneous echogenic mass, measuring 12 x 8 cm, was noted within the amniotic cavity, there was no evidence of pathological flow through the mass on color Doppler. After admittance to the hospital, the patient complained of regular pains, weakness and collapsed with signs of hemorrhagic shock. Repeated ultrasound evaluation showed no change in acoustic texture and size, but the amniotic fluid now had a hyperechoic appearance which revealed increasing intra-amniotic hemorrhage. Because of clinical signs of maternal hemorrhagic shock confirmed by laboratory findings of decreasing red blood parameters, an urgent cesarean section was performed. A female infant weighing 3,070 g, Apgar score 5/7, was delivered. After removal of the placenta there was no sign of abruption, which was confirmed at histopathology. Hemoglobin A was detected in the amniotic fluid by Abt's test. The patient had an uncomplicated postoperative course. The infant developed normally. CONCLUSION: When there are signs of fetal distress or maternal hemorrhagic shock, an urgent cesarean section should be performed.