Surgical resection in patient with teratoma with somatic‐type malignancy transformed into rhabdomyosarcoma resulted in long‐term survival

Introduction Testicular germ cell tumors with somatic‐type malignancy, wherein teratomas transform into sarcomas, is drug resistant and has a poor prognosis. Case presentation A 43‐year‐old man presented with a left testicular tumor, multiple pulmonary metastases, and mediastinal and para‐aortic lym...

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Main Authors: Junji Kitamura, Mitsuhiro Tambo, Ayano Nishijima, Kazuki Masuda, Jimpei Miyakawa, Yu Nakamura, Masachika Fujiwara, Takeshi Kishida, Hiroyuki Ito, Hiroshi Fukuhara
Format: Article
Language:English
Published: Wiley 2023-09-01
Series:IJU Case Reports
Subjects:
Online Access:https://doi.org/10.1002/iju5.12610
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author Junji Kitamura
Mitsuhiro Tambo
Ayano Nishijima
Kazuki Masuda
Jimpei Miyakawa
Yu Nakamura
Masachika Fujiwara
Takeshi Kishida
Hiroyuki Ito
Hiroshi Fukuhara
author_facet Junji Kitamura
Mitsuhiro Tambo
Ayano Nishijima
Kazuki Masuda
Jimpei Miyakawa
Yu Nakamura
Masachika Fujiwara
Takeshi Kishida
Hiroyuki Ito
Hiroshi Fukuhara
author_sort Junji Kitamura
collection DOAJ
description Introduction Testicular germ cell tumors with somatic‐type malignancy, wherein teratomas transform into sarcomas, is drug resistant and has a poor prognosis. Case presentation A 43‐year‐old man presented with a left testicular tumor, multiple pulmonary metastases, and mediastinal and para‐aortic lymph node metastases. The testicular tumors were diagnosed as germ cell tumors. After bleomycin, etoposide, and cisplatin chemotherapy; right upper lobectomy for the pulmonary metastasis; and paclitaxel, ifosfamide, and cisplatin chemotherapy, rapidly progressing mediastinal lymph node metastasis was observed. It was resected at another specialized center owing to the challenging surgical approach. The histopathological diagnosis of the resected tumor was a teratoma with somatic‐type malignancy (rhabdomyosarcoma). Subsequently, left hilar lymph node metastasectomy and left upper lobectomy were performed for the pulmonary metastases. The patient survived for more than 8 years after initial treatment. Conclusion Surgery, although challenging, may yield long‐term survival for patients with testicular germ cell tumors with sarcomatous transformation.
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spelling doaj.art-648f7e7ed8b943fcb4753fec11a4d7cb2023-09-04T00:11:48ZengWileyIJU Case Reports2577-171X2023-09-016530230510.1002/iju5.12610Surgical resection in patient with teratoma with somatic‐type malignancy transformed into rhabdomyosarcoma resulted in long‐term survivalJunji Kitamura0Mitsuhiro Tambo1Ayano Nishijima2Kazuki Masuda3Jimpei Miyakawa4Yu Nakamura5Masachika Fujiwara6Takeshi Kishida7Hiroyuki Ito8Hiroshi Fukuhara9Department of Urology Kyorin University School of Medicine Mitaka Tokyo JapanDepartment of Urology Kyorin University School of Medicine Mitaka Tokyo JapanDepartment of Urology Kyorin University School of Medicine Mitaka Tokyo JapanDepartment of Urology Kyorin University School of Medicine Mitaka Tokyo JapanDepartment of Urology Kyorin University School of Medicine Mitaka Tokyo JapanDepartment of Urology Kyorin University School of Medicine Mitaka Tokyo JapanDepartment of Pathology Kyorin University School of Medicine Mitaka Tokyo JapanDepartment of Urology Kanagawa Cancer Center Yokohama Kanagawa JapanDepartment of Thoracic Surgery Kanagawa Cancer Center Yokohama Kanagawa JapanDepartment of Urology Kyorin University School of Medicine Mitaka Tokyo JapanIntroduction Testicular germ cell tumors with somatic‐type malignancy, wherein teratomas transform into sarcomas, is drug resistant and has a poor prognosis. Case presentation A 43‐year‐old man presented with a left testicular tumor, multiple pulmonary metastases, and mediastinal and para‐aortic lymph node metastases. The testicular tumors were diagnosed as germ cell tumors. After bleomycin, etoposide, and cisplatin chemotherapy; right upper lobectomy for the pulmonary metastasis; and paclitaxel, ifosfamide, and cisplatin chemotherapy, rapidly progressing mediastinal lymph node metastasis was observed. It was resected at another specialized center owing to the challenging surgical approach. The histopathological diagnosis of the resected tumor was a teratoma with somatic‐type malignancy (rhabdomyosarcoma). Subsequently, left hilar lymph node metastasectomy and left upper lobectomy were performed for the pulmonary metastases. The patient survived for more than 8 years after initial treatment. Conclusion Surgery, although challenging, may yield long‐term survival for patients with testicular germ cell tumors with sarcomatous transformation.https://doi.org/10.1002/iju5.12610metastasisrhabdomyosarcomasurgeryteratomatesticular germ cell tumor
spellingShingle Junji Kitamura
Mitsuhiro Tambo
Ayano Nishijima
Kazuki Masuda
Jimpei Miyakawa
Yu Nakamura
Masachika Fujiwara
Takeshi Kishida
Hiroyuki Ito
Hiroshi Fukuhara
Surgical resection in patient with teratoma with somatic‐type malignancy transformed into rhabdomyosarcoma resulted in long‐term survival
IJU Case Reports
metastasis
rhabdomyosarcoma
surgery
teratoma
testicular germ cell tumor
title Surgical resection in patient with teratoma with somatic‐type malignancy transformed into rhabdomyosarcoma resulted in long‐term survival
title_full Surgical resection in patient with teratoma with somatic‐type malignancy transformed into rhabdomyosarcoma resulted in long‐term survival
title_fullStr Surgical resection in patient with teratoma with somatic‐type malignancy transformed into rhabdomyosarcoma resulted in long‐term survival
title_full_unstemmed Surgical resection in patient with teratoma with somatic‐type malignancy transformed into rhabdomyosarcoma resulted in long‐term survival
title_short Surgical resection in patient with teratoma with somatic‐type malignancy transformed into rhabdomyosarcoma resulted in long‐term survival
title_sort surgical resection in patient with teratoma with somatic type malignancy transformed into rhabdomyosarcoma resulted in long term survival
topic metastasis
rhabdomyosarcoma
surgery
teratoma
testicular germ cell tumor
url https://doi.org/10.1002/iju5.12610
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