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Tubal choriocarcinoma presented as ruptured ectopic pregnancy: a case report and review of the literature
BACKGROUND: Tubal choriocarcinoma is an extremely rare but highly malignant trophoblastic tumor, which may be either gestational or non-gestational in origin. Due to atypical clinical manifestations and symptoms similar to ectopic pregnancy, it is easily to be confused with ectopic pregnancy. In add...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488679/ https://www.ncbi.nlm.nih.gov/pubmed/32919475 http://dx.doi.org/10.1186/s12957-020-02021-4 |
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author | Xu, Shengjie Song, Xiaohong Jin, Chengjuan Li, Yanli |
author_facet | Xu, Shengjie Song, Xiaohong Jin, Chengjuan Li, Yanli |
author_sort | Xu, Shengjie |
collection | PubMed |
description | BACKGROUND: Tubal choriocarcinoma is an extremely rare but highly malignant trophoblastic tumor, which may be either gestational or non-gestational in origin. Due to atypical clinical manifestations and symptoms similar to ectopic pregnancy, it is easily to be confused with ectopic pregnancy. In addition, inadequate understanding of this rare disease by clinicians often leads to misdiagnosis or missed diagnosis, which in turn results in delayed treatment or even tumor metastasis. CASE PRESENTATION: This report summarized a case of a woman who was finally diagnosed as tubal choriocarcinoma through the follow-up of serum β hCG levels and histopathological results after undergoing salpingectomy for being misdiagnosed as ectopic pregnancy. Five courses of adjuvant chemotherapy (5-fluorouracil, actinomycin-D, vinorelbine regime) have been administered to the patient in the prevention of any recurrences. During 1-year follow-up, the patient was asymptomatic and presented no evidence of recurrence. CONCLUSIONS: Tubal choriocarcinoma is easily to be confused with ectopic pregnancy. By analyzing this case and previous related cases, we aimed to provide references for clinicians in the diagnosis and treatment of tubal choriocarcinoma. |
format | Online Article Text |
id | pubmed-7488679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74886792020-09-16 Tubal choriocarcinoma presented as ruptured ectopic pregnancy: a case report and review of the literature Xu, Shengjie Song, Xiaohong Jin, Chengjuan Li, Yanli World J Surg Oncol Case Report BACKGROUND: Tubal choriocarcinoma is an extremely rare but highly malignant trophoblastic tumor, which may be either gestational or non-gestational in origin. Due to atypical clinical manifestations and symptoms similar to ectopic pregnancy, it is easily to be confused with ectopic pregnancy. In addition, inadequate understanding of this rare disease by clinicians often leads to misdiagnosis or missed diagnosis, which in turn results in delayed treatment or even tumor metastasis. CASE PRESENTATION: This report summarized a case of a woman who was finally diagnosed as tubal choriocarcinoma through the follow-up of serum β hCG levels and histopathological results after undergoing salpingectomy for being misdiagnosed as ectopic pregnancy. Five courses of adjuvant chemotherapy (5-fluorouracil, actinomycin-D, vinorelbine regime) have been administered to the patient in the prevention of any recurrences. During 1-year follow-up, the patient was asymptomatic and presented no evidence of recurrence. CONCLUSIONS: Tubal choriocarcinoma is easily to be confused with ectopic pregnancy. By analyzing this case and previous related cases, we aimed to provide references for clinicians in the diagnosis and treatment of tubal choriocarcinoma. BioMed Central 2020-09-12 /pmc/articles/PMC7488679/ /pubmed/32919475 http://dx.doi.org/10.1186/s12957-020-02021-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Xu, Shengjie Song, Xiaohong Jin, Chengjuan Li, Yanli Tubal choriocarcinoma presented as ruptured ectopic pregnancy: a case report and review of the literature |
title | Tubal choriocarcinoma presented as ruptured ectopic pregnancy: a case report and review of the literature |
title_full | Tubal choriocarcinoma presented as ruptured ectopic pregnancy: a case report and review of the literature |
title_fullStr | Tubal choriocarcinoma presented as ruptured ectopic pregnancy: a case report and review of the literature |
title_full_unstemmed | Tubal choriocarcinoma presented as ruptured ectopic pregnancy: a case report and review of the literature |
title_short | Tubal choriocarcinoma presented as ruptured ectopic pregnancy: a case report and review of the literature |
title_sort | tubal choriocarcinoma presented as ruptured ectopic pregnancy: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488679/ https://www.ncbi.nlm.nih.gov/pubmed/32919475 http://dx.doi.org/10.1186/s12957-020-02021-4 |
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