Molar pregnancy Flashcards

1
Q

Molar pregnancy

A

Hydatidiform mole is a type of tumour that grows like a pregnancy inside the uterus. This is called a molar pregnancy. There are two types of molar pregnancy: a complete mole and a partial mole.

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2
Q

What is a complete mole?

A

Occurs when two sperm cells fertilise an ovum that contains no genetic material (an “empty ovum”).

These sperm then combine genetic material, and the cells start to divide and grow into a tumour called a complete mole. No foetal material will form.

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3
Q

What is a partial mole?

A

Occurs when two sperm cells fertilise a normal ovum (containing genetic material) at the same time.

The new cell now has three sets of chromosomes (it is a haploid cell). The cell divides and multiplies into a tumour called a partial mole. In a partial mole, some foetal material may form.

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4
Q

Gestational trophoblastic disease

A

A term used to describe a group of pregnancy-related tumours.

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5
Q

What are examples of pre-malignant conditions in Gestational trophoblastic disease?

A

More common = such as partial molar pregnancy and complete molar pregnancy.

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6
Q

What are examples of malignant conditions in Gestational trophoblastic disease?

A

Such as invasive mole, choriocarcinoma, placental trophoblastic site tumour and epithelioid trophoblastic tumour.

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7
Q

Choriocarcinoma

A

A malignancy of the trophoblastic cells of the placenta. It commonly, but not exclusively, co-exists with a molar pregnancy.

This type of GTT characteristically metastasises to the lungs.

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8
Q

Placental site trophoblastic tumour

A

A malignancy of the intermediate trophoblasts, which are normally responsible for anchoring the placenta to the uterus.

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9
Q

Epithelioid trophoblastic tumour

A

A malignancy of the trophoblastic placental cells, which can be very difficult to distinguish from choriocarcinoma. It mimics the cytological features of squamous cell carcinoma

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10
Q

Clinical presentation for molar pregnancies

A

Vaginal bleeding, abdominal pain early in pregnancy.

On examination, the uterus can be larger than expected for gestation, and of a soft, boggy consistency.

Later symptoms - Hyperemesis , Hyperthyroidism and Anaemia

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11
Q

Investigations for molar pregnancy

A

Urine B-hCG
Blood B-hCG levels
Ultrasound Scan
Histological examination of the products of conception

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12
Q

Management of molar pregnancy

A

Suction curettage

However, if the partial mole is of a greater gestation, and is not conducive to surgery, medical evacuation should be recommended – with a urinary B-hCG measurement performed 3 weeks post-treatment.

In all cases, anti-D prophylaxis is recommended post-evacuation if the mother is Rhesus negative.

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13
Q

What is Hyperemesis Gravidarum?

A

The severe form of nausea and vomiting in pregnancy is called hyperemesis gravidarum.

Nausea and vomiting are normal during early pregnancy.

Symptoms usually start from 4 – 7 weeks, are worst around 10 – 12 weeks and resolve by 16 – 20 weeks. Symptoms can persist throughout pregnancy.

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14
Q

What causes nausea and vomiting in pregnancy?

A

The placenta produces hCG during pregnancy. This hormone is thought to be responsible for nausea and vomiting.

Theoretically, higher levels of hCG result in worse symptoms.

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15
Q

Criteria for diagnosis of Hyperemesis gravidarum

A
  • More than 5 % weight loss compared with before pregnancy
  • Dehydration
  • Electrolyte imbalance
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16
Q

What anti emetics are used for the management of hyperemesis gravidarum?

A
  1. Prochlorperazine (stemetil)
  2. Cyclizine
  3. Ondansetron
  4. Metoclopramide
17
Q

Ovarian hyperstimulation syndrome (OHSS)

A

A complication of ovarian stimulation during IVF infertility treatment.

It is associated with the use of hCG to mature the follicles during the final steps of ovarian stimulation.

18
Q

Psychophysiology of Ovarian hyperstimulation syndrome (OHSS)

A

An increase in vascular endothelial growth factor (VEGF) released by the granulosa cells of the follicles.

VEGF increases vascular permeability, causing fluid to leak from capillaries. Fluid moves from the intravascular space to the extravascular space. This results in oedema, ascites and hypovolaemia.

The use of gonadotrophins (LH and FSH) during ovarian stimulation results in the development of multiple follicles.

OHSS is provoked by the “trigger injection” of hCG 36 hours before oocyte collection. HCG stimulates the release of VEGF from the follicles.

There is also activation of the renin-angiotensin system.

19
Q

What system is activated in Ovarian hyperstimulation syndrome (OHSS)?

A

Renin-angiotensin system

20
Q

Risk factors for Ovarian hyperstimulation syndrome (OHSS)

A
	Younger age
	Lower BMI
	Raised anti-Müllerian hormone 
	Higher antral follicle count
	Polycystic ovarian syndrome
	Raised oestrogen levels
21
Q

What is anti-Müllerian hormone useful for?

A

Useful marker of ovarian function. Granulosa cells of growing follicles secrete AMH, and its serum levels reflect the remaining follicular pool and thus the remaining length of a woman’s reproductive lifespan.

22
Q

Women are individually assessed for their risk of developing OHSS, how are the patients monitored for OHSS?

A
  1. Serum oestrogen levels (higher levels indicate a higher risk)
  2. Ultrasound monitor of the follicles (higher number and larger size indicate a higher risk)
23
Q

Features of OHSS

A
	Abdominal pain and bloating
	Nausea and vomiting
	Diarrhoea
	Hypotension
	Hypovolaemia
	Ascites
	Pleural effusions
	Renal failure
	Peritonitis 
	Prothrombotic state (risk of DVT and PE)
24
Q

Difference between early & late OHSS.

A

Early OHSS presents within 7 days of the hCG injection.

Late OHSS presents from 10 days onwards.

25
Q

What are the 4 classifications for the severity of OHSS based on symptoms?

A
  1. Mild
  2. Moderate
  3. Severe
  4. Critical
26
Q

What is the symptoms of mild OHSS?

A

Abdominal pain and bloating

27
Q

What is the symptoms of Moderate OHSS?

A

Nausea and vomiting with ascites seen on ultrasound

28
Q

What is the symptoms of Severe OHSS?

A

Ascites, low urine output (oliguria), low serum albumin, high potassium and raised haematocrit (>45%)

29
Q

What is the symptoms of Critical OHSS?

A

Tense ascites, no urine output (anuria), thromboembolism and acute respiratory distress syndrome (ARDS)

30
Q

Management of OHSS

A
  1. Oral fluids
  2. Monitoring of urine output
  3. LMWHs (to prevent thromboembolism)
  4. Ascitic fluid removal if required
  5. IV colloids
31
Q

Haematocrit

A

Is the concentration of red blood cells in the blood.

When the haematocrit goes up, this indicates less fluid in the intravascular space, as the blood is becoming more concentrated. Raised haematocrit can indicate dehydration.

32
Q

What does a raised haematocrit suggest?

A

can indicate dehydration