EP11.19: A rare presentation: suspected hemolytic uremic syndrome in early pregnancy

Hemolytic uremic syndrome (HUS) is a rare pregnancy complication (1/25,000) with microangiopathy as a hallmark feature. Differentiating HUS from other obstetric complications poses a significant challenge. We present the case of a patient at 17 weeks gestation presenting with microangiopathy. A 38 year old pregnant woman, G4P1A3 with prior miscarriages, an ectopic pregnancy, and one Caesarean section at term, presented at 17 weeks with cephalea, vomiting, and visual blur (4 days). Current pregnancy was IVF induced and the patient reported enoxaparin and aspirin use for thromboprophylaxis. Past medical history was unremarkable for hypertension, allergies, or substance abuse, although she reported recent food poisoning. Physical examination revealed signs of microangiopathy, including pale conjunctivae, palpebral edema, ecchymosis, and proteinuria. Blood pressure was normal (100/80 mmHg). Ultrasound confirmed fetal viability. Laboratory findings were concerning for microangiopathic hemolytic anemia with a hemoglobin of 6.8 g/dL, a platelet count of 36,000/μL, and a markedly elevated creatinine level of 637.79 μmol/L. Liver function tests were within normal limits. Atypical HELLP syndrome or HUS were suspected given the clinical presentation and laboratory abnormalities. The patient received transfusions and underwent Caesarean section due to ongoing concerns, the surgery was complicated by uterine atony, requiring medical and vascular procedures to achieve hemostasis. Postoperatively, deteriorating renal function required hemodialysis. The diagnosis of HUS was ultimately suspected due to the persistent renal dysfunction despite delivery and the absence of ADAMTS testing, which was unavailable. In conclusion, this case underscores the importance of including HUS in the differential diagnosis for pregnant women presenting with anemia, thrombocytopenia, and acute renal failure. Early diagnosis is crucial due to the potential for severe maternal complications.

Authors

Institutions

Publication Details

Journal
Ultrasound in Obstetrics and Gynecology
Published
2024-09-01
DOI
https://doi.org/10.1002/uog.28542
Primary Topic
Complement system in diseases
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

EP11.19: A rare presentation: suspected hemolytic uremic syndrome in early pregnancy

Mariem Garci, Cyrine Belghith, Aziza Akacha, Olfa Slimani et al.
Ultrasound in Obstetrics and Gynecology
Complement system in diseases
article

EP11.19: A rare presentation: suspected hemolytic uremic syndrome in early pregnancy

Mariem Garci, Cyrine Belghith, Aziza Akacha, Olfa Slimani, Ons Mrad, Nour Zhiri, Olfa Ben Moumen, J. Amich, Chourouk Yahyaoui, A. Azzouni, N Mathlouthi, Mounir Makni
article en

Abstract

Hemolytic uremic syndrome (HUS) is a rare pregnancy complication (1/25,000) with microangiopathy as a hallmark feature. Differentiating HUS from other obstetric complications poses a significant challenge. We present the case of a patient at 17 weeks gestation presenting with microangiopathy. A 38 year old pregnant woman, G4P1A3 with prior miscarriages, an ectopic pregnancy, and one Caesarean section at term, presented at 17 weeks with cephalea, vomiting, and visual blur (4 days). Current pregnancy was IVF induced and the patient reported enoxaparin and aspirin use for thromboprophylaxis. Past medical history was unremarkable for hypertension, allergies, or substance abuse, although she reported recent food poisoning. Physical examination revealed signs of microangiopathy, including pale conjunctivae, palpebral edema, ecchymosis, and proteinuria. Blood pressure was normal (100/80 mmHg). Ultrasound confirmed fetal viability. Laboratory findings were concerning for microangiopathic hemolytic anemia with a hemoglobin of 6.8 g/dL, a platelet count of 36,000/μL, and a markedly elevated creatinine level of 637.79 μmol/L. Liver function tests were within normal limits. Atypical HELLP syndrome or HUS were suspected given the clinical presentation and laboratory abnormalities. The patient received transfusions and underwent Caesarean section due to ongoing concerns, the surgery was complicated by uterine atony, requiring medical and vascular procedures to achieve hemostasis. Postoperatively, deteriorating renal function required hemodialysis. The diagnosis of HUS was ultimately suspected due to the persistent renal dysfunction despite delivery and the absence of ADAMTS testing, which was unavailable. In conclusion, this case underscores the importance of including HUS in the differential diagnosis for pregnant women presenting with anemia, thrombocytopenia, and acute renal failure. Early diagnosis is crucial due to the potential for severe maternal complications.

Ultrasound in Obstetrics and GynecologyVol. 64(S1)
Tunis University (TN), Hôpital Charles-Nicolle (TN), Faculté de médecine de Tunis, Tunis El Manar University (TN)
Good health and well-being
Openalex Percentile: Top 81%
Complement system in diseases
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.