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Accurate short tandem repeat analysis for confirmation of rare gestational adrenal choriocarcinoma: a case report

Rare adrenal choriocarcinoma should be identified as gestational or nongestational choriocarcinoma because of their different treatment and prognosis. A 29-year-old parous women underwent curettage and right-oviduct resection successively due to irregular vaginal bleeding and positive human chorioni...

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Autores principales: Zhao, Lanbo, Ma, Sijia, Wang, Yiran, Feng, Xue, Li, Jie, Wang, Qiuping, Wang, Yawen, Liu, Shuhua, Li, Qiling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798973/
https://www.ncbi.nlm.nih.gov/pubmed/35117739
http://dx.doi.org/10.21037/tcr.2020.04.08
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author Zhao, Lanbo
Ma, Sijia
Wang, Yiran
Feng, Xue
Li, Jie
Wang, Qiuping
Wang, Yawen
Liu, Shuhua
Li, Qiling
author_facet Zhao, Lanbo
Ma, Sijia
Wang, Yiran
Feng, Xue
Li, Jie
Wang, Qiuping
Wang, Yawen
Liu, Shuhua
Li, Qiling
author_sort Zhao, Lanbo
collection PubMed
description Rare adrenal choriocarcinoma should be identified as gestational or nongestational choriocarcinoma because of their different treatment and prognosis. A 29-year-old parous women underwent curettage and right-oviduct resection successively due to irregular vaginal bleeding and positive human chorionic gonadotropin (HCG). Postoperative pathological examinations revealed no intrauterine and extrauterine pregnancy. After that, HCG continued to rise. A 7.6×10.3×11.0 cm mass was present in the left adrenal gland with an uneven inner density and a complete capsule by computed tomography (CT). A biopsy was performed on the mass, which showed us choriocarcinoma. Seven cycles of chemotherapy made her complete response and under supervision. Recurrent diagnosis was done after 3 months. The tumor specimen, the patient’s blood, and her husband’s blood were drawn for short tandem repeat (STR) analysis using polymerase chain reaction amplification kit. The genotype of the tumor cells was both maternal and patrilineal, which led to the diagnosis of adrenal gestational choriocarcinoma. The patient was scheduled for adrenalectomy and various chemotherapeutic interventions before and after operation. She achieved complete response and was being followed up again. STR analysis first aids in precise classification of this rare adrenal choriocarcinoma. We encourage using the method to analyze choriocarcinoma outside reproductive organs.
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spelling pubmed-87989732022-02-02 Accurate short tandem repeat analysis for confirmation of rare gestational adrenal choriocarcinoma: a case report Zhao, Lanbo Ma, Sijia Wang, Yiran Feng, Xue Li, Jie Wang, Qiuping Wang, Yawen Liu, Shuhua Li, Qiling Transl Cancer Res Case Report Rare adrenal choriocarcinoma should be identified as gestational or nongestational choriocarcinoma because of their different treatment and prognosis. A 29-year-old parous women underwent curettage and right-oviduct resection successively due to irregular vaginal bleeding and positive human chorionic gonadotropin (HCG). Postoperative pathological examinations revealed no intrauterine and extrauterine pregnancy. After that, HCG continued to rise. A 7.6×10.3×11.0 cm mass was present in the left adrenal gland with an uneven inner density and a complete capsule by computed tomography (CT). A biopsy was performed on the mass, which showed us choriocarcinoma. Seven cycles of chemotherapy made her complete response and under supervision. Recurrent diagnosis was done after 3 months. The tumor specimen, the patient’s blood, and her husband’s blood were drawn for short tandem repeat (STR) analysis using polymerase chain reaction amplification kit. The genotype of the tumor cells was both maternal and patrilineal, which led to the diagnosis of adrenal gestational choriocarcinoma. The patient was scheduled for adrenalectomy and various chemotherapeutic interventions before and after operation. She achieved complete response and was being followed up again. STR analysis first aids in precise classification of this rare adrenal choriocarcinoma. We encourage using the method to analyze choriocarcinoma outside reproductive organs. AME Publishing Company 2020-05 /pmc/articles/PMC8798973/ /pubmed/35117739 http://dx.doi.org/10.21037/tcr.2020.04.08 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Case Report
Zhao, Lanbo
Ma, Sijia
Wang, Yiran
Feng, Xue
Li, Jie
Wang, Qiuping
Wang, Yawen
Liu, Shuhua
Li, Qiling
Accurate short tandem repeat analysis for confirmation of rare gestational adrenal choriocarcinoma: a case report
title Accurate short tandem repeat analysis for confirmation of rare gestational adrenal choriocarcinoma: a case report
title_full Accurate short tandem repeat analysis for confirmation of rare gestational adrenal choriocarcinoma: a case report
title_fullStr Accurate short tandem repeat analysis for confirmation of rare gestational adrenal choriocarcinoma: a case report
title_full_unstemmed Accurate short tandem repeat analysis for confirmation of rare gestational adrenal choriocarcinoma: a case report
title_short Accurate short tandem repeat analysis for confirmation of rare gestational adrenal choriocarcinoma: a case report
title_sort accurate short tandem repeat analysis for confirmation of rare gestational adrenal choriocarcinoma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798973/
https://www.ncbi.nlm.nih.gov/pubmed/35117739
http://dx.doi.org/10.21037/tcr.2020.04.08
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