Mediastinal yolk sac tumor infiltrating the heart

Background: As a rare tumor, yolk sac tumor is a type of neoplasm that appears like the yolk sac, extraembryonic mesenchyme, and allantois. The mediastinum is the second most frequent area after the gonadal area. Case report: We present an extremely rare case of 15 years old boy with mediastinal yol...

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Опубліковано в: :Experimental Oncology
Дата:2018
Автори: Imaniar, R., Syahruddin, E., Soepandi, P.Z., Putra, A.C., Nurwidya, F.
Формат: Стаття
Мова:Англійська
Опубліковано: Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України 2018
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Онлайн доступ:https://nasplib.isofts.kiev.ua/handle/123456789/139256
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Назва журналу:Digital Library of Periodicals of National Academy of Sciences of Ukraine
Цитувати:Mediastinal yolk sac tumor infiltrating the heart / R. Imaniar, E. Syahruddin, P.Z. Soepandi, A.C. Putra, F. Nurwidya // Experimental Oncology. — 2018 — Т. 40, № 1. — С. 82-84. — Бібліогр.: 16 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
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author Imaniar, R.
Syahruddin, E.
Soepandi, P.Z.
Putra, A.C.
Nurwidya, F.
author_facet Imaniar, R.
Syahruddin, E.
Soepandi, P.Z.
Putra, A.C.
Nurwidya, F.
citation_txt Mediastinal yolk sac tumor infiltrating the heart / R. Imaniar, E. Syahruddin, P.Z. Soepandi, A.C. Putra, F. Nurwidya // Experimental Oncology. — 2018 — Т. 40, № 1. — С. 82-84. — Бібліогр.: 16 назв. — англ.
collection DSpace DC
container_title Experimental Oncology
description Background: As a rare tumor, yolk sac tumor is a type of neoplasm that appears like the yolk sac, extraembryonic mesenchyme, and allantois. The mediastinum is the second most frequent area after the gonadal area. Case report: We present an extremely rare case of 15 years old boy with mediastinal yolk sac tumor. The boy came with the chief complaint of swelling of the neck and face. Computed tomography scan of the chest revealed bulky mass with a cystic component that infiltrated the heart. The diagnosis of mediastinal yolk sac tumor was made after core needle biopsy. Histopathologic analysis revealed tumor mass with solid and microcystic structure and pleomorphic nucleus within the tumor cells. Laboratory finding showed elevated serum alpha-fetoprotein level reaching more than 8000 ng/ml. Echocardiography revealed a mass in the right atrium. The patient condition was rapidly deteriorated due to his vena cava superior syndrome. Unfortunately, the patient died two days after diagnosis and we did not have the chance to do the therapy. Conclusion: Mediastinal yolk sac tumor is a rare malignancy that requires comprehensive management. The diagnosis should be made based on histopathological findings with the addition of thoracic computer tomography scan to assess the degree of infiltration to surrounding organ. A life-threatening condition such as vena cava superior syndrome should be assessed promptly to allow for immediate treatment.
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publisher Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України
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spelling Imaniar, R.
Syahruddin, E.
Soepandi, P.Z.
Putra, A.C.
Nurwidya, F.
2018-06-19T21:19:20Z
2018-06-19T21:19:20Z
2018
Mediastinal yolk sac tumor infiltrating the heart / R. Imaniar, E. Syahruddin, P.Z. Soepandi, A.C. Putra, F. Nurwidya // Experimental Oncology. — 2018 — Т. 40, № 1. — С. 82-84. — Бібліогр.: 16 назв. — англ.
1812-9269
https://nasplib.isofts.kiev.ua/handle/123456789/139256
Background: As a rare tumor, yolk sac tumor is a type of neoplasm that appears like the yolk sac, extraembryonic mesenchyme, and allantois. The mediastinum is the second most frequent area after the gonadal area. Case report: We present an extremely rare case of 15 years old boy with mediastinal yolk sac tumor. The boy came with the chief complaint of swelling of the neck and face. Computed tomography scan of the chest revealed bulky mass with a cystic component that infiltrated the heart. The diagnosis of mediastinal yolk sac tumor was made after core needle biopsy. Histopathologic analysis revealed tumor mass with solid and microcystic structure and pleomorphic nucleus within the tumor cells. Laboratory finding showed elevated serum alpha-fetoprotein level reaching more than 8000 ng/ml. Echocardiography revealed a mass in the right atrium. The patient condition was rapidly deteriorated due to his vena cava superior syndrome. Unfortunately, the patient died two days after diagnosis and we did not have the chance to do the therapy. Conclusion: Mediastinal yolk sac tumor is a rare malignancy that requires comprehensive management. The diagnosis should be made based on histopathological findings with the addition of thoracic computer tomography scan to assess the degree of infiltration to surrounding organ. A life-threatening condition such as vena cava superior syndrome should be assessed promptly to allow for immediate treatment.
en
Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України
Experimental Oncology
Case report
Mediastinal yolk sac tumor infiltrating the heart
Article
published earlier
spellingShingle Mediastinal yolk sac tumor infiltrating the heart
Imaniar, R.
Syahruddin, E.
Soepandi, P.Z.
Putra, A.C.
Nurwidya, F.
Case report
title Mediastinal yolk sac tumor infiltrating the heart
title_full Mediastinal yolk sac tumor infiltrating the heart
title_fullStr Mediastinal yolk sac tumor infiltrating the heart
title_full_unstemmed Mediastinal yolk sac tumor infiltrating the heart
title_short Mediastinal yolk sac tumor infiltrating the heart
title_sort mediastinal yolk sac tumor infiltrating the heart
topic Case report
topic_facet Case report
url https://nasplib.isofts.kiev.ua/handle/123456789/139256
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AT putraac mediastinalyolksactumorinfiltratingtheheart
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