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A Diagnosis of Choriocarcinoma in a Parturient Presenting With Intracranial Hemorrhage

Choriocarcinoma in a viable pregnancy is uncommon. The diagnosis can easily be missed when there is an explanation for the clinical symptoms that the cancer can mimic. We present the case of a primigravid patient whose choriocarcinoma was initially missed as a result of seemingly obvious explanation...

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Autores principales: Romeo, Deborah A., Gutman, David A., Sirianni, Joel, Marotta, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993443/
https://www.ncbi.nlm.nih.gov/pubmed/35464325
http://dx.doi.org/10.14740/jmc3898
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author Romeo, Deborah A.
Gutman, David A.
Sirianni, Joel
Marotta, Michael
author_facet Romeo, Deborah A.
Gutman, David A.
Sirianni, Joel
Marotta, Michael
author_sort Romeo, Deborah A.
collection PubMed
description Choriocarcinoma in a viable pregnancy is uncommon. The diagnosis can easily be missed when there is an explanation for the clinical symptoms that the cancer can mimic. We present the case of a primigravid patient whose choriocarcinoma was initially missed as a result of seemingly obvious explanations for her atypical history and disease manifestation. The patient is a Caucasian female at 30 weeks and 5 days of gestation who presented with persistent headaches and new-onset tonic-clonic seizures found on brain magnetic resonance imaging (MRI) to have a left intracranial hematoma, a 5 mm midline shift, and multiple foci of restricted diffusion. Cerebral angiogram demonstrated arteriovenous malformations (AVMs). The fetus was emergently delivered 1 week into hospitalization for non-reassuring fetal heart tracings in the setting of maternal lethargy secondary to continued AVM hemorrhage. The patient’s hospital course was complicated by four episodes of intracranial bleeding and edema requiring neurosurgical intervention. Three weeks after hospitalization she was discharged to a rehabilitation center, shortly after which placental biopsy demonstrated choriocarcinoma. MRI after readmission demonstrated extensive metastatic disease and human chorionic gonadotropin (hCG) levels were greater than 225,000 mIU/mL. Despite two additional neurosurgical procedures and extensive chemotherapy the patient died 3 months after initial presentation. Choriocarcinoma is extremely rare in viable pregnancies, but it should be considered when a parturient presents with intracranial bleeding. A high level of suspicion and serial serum hCG levels may lead to early and potentially life-saving multidrug chemotherapy. With a broader differential, earlier hCG measurement, and earlier treatment, our patient may have survived.
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spelling pubmed-89934432022-04-22 A Diagnosis of Choriocarcinoma in a Parturient Presenting With Intracranial Hemorrhage Romeo, Deborah A. Gutman, David A. Sirianni, Joel Marotta, Michael J Med Cases Case Report Choriocarcinoma in a viable pregnancy is uncommon. The diagnosis can easily be missed when there is an explanation for the clinical symptoms that the cancer can mimic. We present the case of a primigravid patient whose choriocarcinoma was initially missed as a result of seemingly obvious explanations for her atypical history and disease manifestation. The patient is a Caucasian female at 30 weeks and 5 days of gestation who presented with persistent headaches and new-onset tonic-clonic seizures found on brain magnetic resonance imaging (MRI) to have a left intracranial hematoma, a 5 mm midline shift, and multiple foci of restricted diffusion. Cerebral angiogram demonstrated arteriovenous malformations (AVMs). The fetus was emergently delivered 1 week into hospitalization for non-reassuring fetal heart tracings in the setting of maternal lethargy secondary to continued AVM hemorrhage. The patient’s hospital course was complicated by four episodes of intracranial bleeding and edema requiring neurosurgical intervention. Three weeks after hospitalization she was discharged to a rehabilitation center, shortly after which placental biopsy demonstrated choriocarcinoma. MRI after readmission demonstrated extensive metastatic disease and human chorionic gonadotropin (hCG) levels were greater than 225,000 mIU/mL. Despite two additional neurosurgical procedures and extensive chemotherapy the patient died 3 months after initial presentation. Choriocarcinoma is extremely rare in viable pregnancies, but it should be considered when a parturient presents with intracranial bleeding. A high level of suspicion and serial serum hCG levels may lead to early and potentially life-saving multidrug chemotherapy. With a broader differential, earlier hCG measurement, and earlier treatment, our patient may have survived. Elmer Press 2022-04 2022-03-25 /pmc/articles/PMC8993443/ /pubmed/35464325 http://dx.doi.org/10.14740/jmc3898 Text en Copyright 2022, Romeo et al. https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Romeo, Deborah A.
Gutman, David A.
Sirianni, Joel
Marotta, Michael
A Diagnosis of Choriocarcinoma in a Parturient Presenting With Intracranial Hemorrhage
title A Diagnosis of Choriocarcinoma in a Parturient Presenting With Intracranial Hemorrhage
title_full A Diagnosis of Choriocarcinoma in a Parturient Presenting With Intracranial Hemorrhage
title_fullStr A Diagnosis of Choriocarcinoma in a Parturient Presenting With Intracranial Hemorrhage
title_full_unstemmed A Diagnosis of Choriocarcinoma in a Parturient Presenting With Intracranial Hemorrhage
title_short A Diagnosis of Choriocarcinoma in a Parturient Presenting With Intracranial Hemorrhage
title_sort diagnosis of choriocarcinoma in a parturient presenting with intracranial hemorrhage
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993443/
https://www.ncbi.nlm.nih.gov/pubmed/35464325
http://dx.doi.org/10.14740/jmc3898
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