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Gestational trophoblastic disease: an update

  • Special Section : Cancer in Pregnancy
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Abstract

Gestational trophoblastic diseases (GTD) encompass a spectrum of rare pre-malignant and malignant entities originating from trophoblastic tissue. This updated review will highlight important radiological features, pathology and classification, and provide insight into the clinical management of these uncommon disorders. There is a wide geographic variation with the incidence of hydatidiform mole varying between 0.57 and 2 per 1000 pregnancies. The use of ultrasound (US) in the management of early pregnancy symptoms and complications has positively impacted the earlier detection of these diseases and resulted in diminished morbidity. Additional imaging modalities are reserved for problem solving or assessment of pulmonary manifestations of molar pregnancy. Having an awareness of their pleomorphic sonographic presentation and additional pathology that can mimic GTD is critical to avoiding pitfalls. Histologic and molecular analysis further aids in differential diagnosis. Gestational trophoblastic neoplasia (GTN) is inclusive of all malignant GTDs, and arises after 20% of molar pregnancies but can also be seen with non-molar gestations. Biochemical monitoring with human chorionic gonadotrophin is imperative for ongoing monitoring and surveillance and allows early detection of this entity. Doppler US is used for confirmation of diagnosis with magnetic resonance imaging (MRI) reserved for problem solving or assessment of myometrial invasion. This is of heightened relevance in patients undergoing surgical management. Cross sectional imaging is reserved for patients in the setting of GTN for the purposes of staging, prognostication and in the setting of recurrent disease. This may require a combination of computed tomography, MRI and positron emission tomography. Doppler US can provide insight into chemotherapeutic response/predict resistance in patients with GTN. As our understanding of these disorders evolves, there has been maturation in management options with a shift from traditional chemotherapy to innovative immunotherapy, particularly in the setting of resistant or high-risk disease.

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Appendix

Appendix

Glossary of abbreviations

hCG

Human chorionic gonadotrophin

GTD

Gestational trophoblastic disease

GTN

Gestational trophoblastic neoplasia

HM

Hydatidiform mole

PHM

Partial hydatidiform mole

CHM

Complete hydatidiform mole

IHM

Invasive hydatidiform mole

PI

Pulsatility index

RI

Resistive index

UAPI

Uterine artery pulsatility index

RPOC

Retained products of conception

PID

Pelvic inflammatory disease

MRI

Magnetic resonance imaging

CS

Caesarian section

PMD

Placental mesenchymal dysplasia

IUGR

Intra uterine growth retardation

GCC

Gestational choriocarcinoma

MTT

Mixed trophoblastic tumour

PSTT

Placental site trophoblastic tumour

ETT

Epithelioid trophoblastic tumour

AV

Arteriovenous

AVM

Arteriovenous malformation

CXR

Chest X-ray

GGO

Ground glass opacity

MRI protocol for imaging pelvic GTD

Technique

Pulse sequence

FOV (cm)

Section thickness (mm)

Matrix

Coronal T2W

SSFSE or TSE

36–40

6, skip 0.5–1 mm

256 × 256

Sagittal T2W (no FS)

TSE or FSE

24–26

4

256 × 256

Sagittal DWI

b (50,500,1000)

28–32

4

80–128 × 80–128

Axial oblique T2W (perpendicular to long axis of uterus)

TSE or FSE

24–26

3–4, skip 0.5 mm

256–320 × 256–320

Axial oblique DWI in same plane as above

b (50,500,1000)

28–32

4

80–128 × 80–128

Axial T1W from bifurcation to perineum

TSE or FSE

30–34

5, skip 1 mm

256–320 × 256 -320

Sagittal pre and post contrast T1W

3D GRE

28

4

256 × 192

Axial oblique delayed post contrast (180 s)

3D GRE

28

3–4

256–320 × 192–224

Axial delayed post gad T1W

3D GRE

28

6

256 × 192

  1. FOV  field of view, FSE  fast spin echo, GRE gradient echo, SSFSE single-shot fast spin-echo, T1W  T1 weighted imaging, TSE turbo spin-echo, T2W T2 weighted imaging

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Chawla, T., Bouchard-Fortier, G., Turashvili, G. et al. Gestational trophoblastic disease: an update. Abdom Radiol 48, 1793–1815 (2023). https://doi.org/10.1007/s00261-023-03820-5

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