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©The Author(s) 2025.
World J Clin Pediatr. Dec 9, 2025; 14(4): 106219
Published online Dec 9, 2025. doi: 10.5409/wjcp.v14.i4.106219
Published online Dec 9, 2025. doi: 10.5409/wjcp.v14.i4.106219
Table 1 Gestational alloimmune liver disease cases summary table
| Case 1 | Case 2 | Case 3 | Case 4 | |
| Mothers’ characteristics | 26-year-old, gravida 2, para 2 | 34-year-old, gravida 5, para 3A2 | 31-year-old, gravida 2, para 1A1 | 32-year-old, gravida 2, para 0A1, N-methyl-D-aspartate encephalitis at 30 gestation weeks |
| Antenatal findings | None | Oligoamnios, asymmetric intrauterine growth restriction | None | Intrauterine growth restriction |
| Term of birth (weeks of gestation) | 39 | 37 | 33 | 34 |
| Preterm birth cause | N/A | N/A | Placental abruption | Maternal encephalitis |
| Major clinical presentation | Hypoglycemia | Hypoglycemia | Hypoglycemia, birth asphyxia, hepatorenal syndrome, hepatomegaly | Hypoglycemia |
| Laboratory findings | Thrombocytopenia, coagulopathy, hyperammonemia, iron saturation level 86% | Thrombocytopenia, cholestasis, high ferritin (4103 μg/L) | Thrombocytopenia, cholestasis, coagulopathy, hypoalbuminemia, high ferritin (3347 μg/L), iron saturation level 88% | Thrombocytopenia, cholestasis, coagulopathy, hypoalbuminemia, high ferritin (2515 μg/L) |
| Liver ultrasound findings | Portosystemic shunt: Patent ductus venosus | Portosystemic shunt: Patent ductus venosus | Heterogenous liver | Heterogenous liver, portosystemic shunt: Patent ductus venosus |
| Magnetic resonance imaging findings | Not performed | No hepatic or extrahepatic siderosis | No hepatic siderosis. Nonspecific for GALD | Hepatic siderosis |
| Salivary glands pathology | No iron deposits | No iron deposits | No iron deposits (Prussian blue) | No iron deposits |
| Liver pathology | Fibrosis, remodeling of the hepatic parenchyma, iron overload. Conclusion: GALD confirmed | Portal fibrosis, giant hepatocytes, siderosis. Conclusion: Nonspecific hepatitis | Membrane attack complex negative, fibrosis, siderosis. Conclusion: GALD confirmed | On autopsy: Fibrosis, siderosis +++, siderosis of pancreas |
| Treatments | Embolization of porto-systemic shunt and liver transplantation | None | Two doses of IVIG | Three doses of IVIG. Double volume exchange transfusion. Listed for liver transplantation |
| Outcomes | Normal liver function and normal growth | Spontaneous amelioration of liver function. Now: Normal liver function | Now: Normal liver function | Dead from cerebral hemorrhage |
| Subsequent pregnancy | No | No | Yes | Yes |
| Antenatal IVIG | N/A | N/A | Yes (14-16-18-19 weeks then every week) | Yes |
| Outcome for subsequent pregnancy | N/A | N/A | Healthy child | Healthy child |
- Citation: Helali N, Gagnon H, Álvarez F. Gestational alloimmune liver disease reconsidered: Advocating for a new nomenclature and enhanced diagnosis accuracy. World J Clin Pediatr 2025; 14(4): 106219
- URL: https://www.wjgnet.com/2219-2808/full/v14/i4/106219.htm
- DOI: https://dx.doi.org/10.5409/wjcp.v14.i4.106219
