abstract no : 160 abstract id : iria -1141 a case report on immune hydrops fetalis

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ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

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Page 1: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

ABSTRACT NO : 160

ABSTRACT ID : IRIA -1141

A CASE REPORT ON IMMUNE HYDROPS FETALIS

Page 2: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

INTRODUCTION

Hydrops fetalis is a condition in the fetus characterized by an abnormal collection of fluid with at least  two of the following:

1. Edema (fetal anasarca)

2. Ascites (usually surrounding urinary bladder)

3. Pleural effusion

4. Pericardial effusion₍₁₎

Hydrops fetalis is found in about 1 per 700 births and is categorized as :

• Immune hydrops ~10-20%

• Nonimmune hydrops ~ 80-90%₍₁₎

Page 3: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

Hydrops fetalis is typically diagnosed during ultrasound evaluation for other complaints such as :

1. Polyhydraminos

2. Large for Gestational Age

3. Fetal tachycardia

4. Decreased fetal movement

5. Abnormal serum screening

6. Antenatal hemorrhage₍₁₎

Page 4: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

Immune hydrops foetalis results from haemolysis from isoimmunisation. Individuals who lack a specific red cell antigen (like Rh antigen) can potentially produce an antibody when exposed to that antigen

The antibody may prove harmful to the individual in case of a blood transfusion or to a foetus when a mother (Rh negative) conceives. In these cases, the mother could be sensitized if enough erythrocytes from the Rh positive foetus reach her circulation to elicit an immune response(fig 1)₍₁₎.

Case report of a pregnant women is presented, where diagnosis of hydrops fetalis with was established during antenatal period

FIG : 1

Page 5: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

CASE REPORT A 27 year old female, pregnant for second time, reported to

the hospital OPD for routine antenatal check up.

Patient was in second trimester of pregnancy. She had history of an abortion in the past. Patient was not given any prophylactic anti-D immunoglobulin therapy after the abortion.

The routine blood and urine investigations were normal. Her blood group was B negative. Indirect Coomb's test was positive. Serology for TORCH was negative both for IgG and IgM antibodies.

Page 6: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

Increased amniotic fluid volumes(FIG:2)

larger placental size (placentomegaly) / increased placental thickness (placental oedema) >6cm (FIG :2)

FIG : 2

PLACENTA

Page 7: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

presence of a foetal bilateral pleural  effusion& Ascites(FIG:3)

FIG: 3

Page 8: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

An elevated peak systolic velocity (PSV) measured in the middle cerebral artery (MCA) is associated with 100% sensitivity in predicting moderate to severe anaemia non invasively. (FIG:4)

FIG : 4

Page 9: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

BPD is highly variable large for gestational age in this case (FIG : 6)

Scalp Thickness more than 5mm(FIG:5)

FIG :5

FIG : 6

Page 10: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

Skin Thickness in abdomen >5mm with free fluid in the abdominal cavity (Ascites)(FIG : 7)

Abdominal Circumference is also increased for gestational age(FIG:8)

FIG : 7

FIG : 8

Page 11: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

Sagittal section of abdomen showing gross Ascites surrounding the intestinal loops(FIG:09)

FIG : 09

Page 12: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

Coronal section of chest and abdomen showing Pleural effusion and Ascites (FIG:10)

FIG : 10

Page 13: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

3D image showing intrauterine fetus with hydrops fetalis(FIG:11)

FIG : 11

Page 14: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

Keeping in view the past history of abortion, Rh negative status of mother and ultrasonographic features described above, a diagnosis of immune hydrops fetalis was made.

As per the desire of the couple, pregnancy was terminated in view of poor prognosis of the foetus. Anti-D immunoglobulin was administered to the patient immediately after termination of pregnancy.

Page 15: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

DISCUSSION

Pathological changes

(depends on severity )

severely affected foetus

subcutaneous oedema and effusion into the serous cavities

the placenta is also markedly oedematous, boggy and enlarged₍₂₎

Excessive haemolysis

marked erythroid hyperplasia of the bone marrow and extramedullary haematopoiesis

hepatosplenomegaly cause hepaticdysfunction ₍₂₎.

Hydrothorax and Ascites

compromise respiration after birth or leadto severe dystocia as a consequence of the greatlyenlarged abdomen.₍₂₎

Page 16: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

Treatment Choice of treatment depends upon the time of development, diagnosis and the

severity of hydrops

1. If the condition is very severe, early pregnancy(less than 24 weeks of pregnancy),sinusoidal fetal heart rate------Elective termination of pregnancy is considered

2. If the gestational age is between 24 and 34 weeks, fetal anemia-------correction of anemia with intrauterine transfusion is considered

3. If the gestational age is above 34 weeks ,with confirmation of lung maturity fetus is delivered ------postnatal exchange transfusion is done₍₃₎.

4. Transplacental drug therapy for treating arrhythmia like digoxin, amiodarone etc

5. Invasive procedures like ultrasound guided fetal blood/albumin transfusion, ultrasound guided drainage procedures for Ascites ,pleural effusion etc

A team approach using obstetric imagers, maternal fetal medicine specialists, neonatologists and geneticists can help in case management₍₃

Page 17: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

Conclusion: Hydrops represents a terminal stage for many conditions, majority

of which are fetal in origin

Onset of hydrops signifies fetal decompensation

A comprehensive team approach must be done in management and future counseling

Prevention of the hydrops is by usage of Anti D immunoglobulin prophylaxis and prediction of fetal Rh status antenatally by fetal karyotyping

Page 18: ABSTRACT NO : 160 ABSTRACT ID : IRIA -1141 A CASE REPORT ON IMMUNE HYDROPS FETALIS

References:

1. Wilkins, I. Nonimmune hydrops. In Creasy and Resnick's Maternal Fetal- Medicine Principles and Practice sixth ed.Ed Creasy R et al. , 2009, Saunders. pp505-517.

2. Nicolini U, Nicolaides P, Tannirandorn Y, Fisk N, Nasrat H, Rodeck CH. Fetal liver dyfunction in Rh alloimmunization. Br J Obstet Gynaecol 1991 ; 98 : 287

3. Bianchi DW, Crombleholme TM, D'Alton ME. Fetology: Diagnosis & Management of the Fetal Patient.1st ed McGraw-Hill Professional 2000 pp 959-965