Klinefelter Syndrome with Poor Risk Extragonadal Germ Cell Tumor

Germ cell tumors are the most common malignancy in men aged 15-35 years old, with a small percentage presenting in an extragonadal location. These tumors are seldom identified in the gastrointestinal tract. There is increased risk of extragonadal germ cell tumors (EGCT) in men with Klinefelter syndr...

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Main Authors: Jeremy A. Konheim, Jonathan A. Israel, Scott E. Delacroix
Format: Article
Language:English
Published: Elsevier 2017-01-01
Series:Urology Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2214442016301127
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author Jeremy A. Konheim
Jonathan A. Israel
Scott E. Delacroix
author_facet Jeremy A. Konheim
Jonathan A. Israel
Scott E. Delacroix
author_sort Jeremy A. Konheim
collection DOAJ
description Germ cell tumors are the most common malignancy in men aged 15-35 years old, with a small percentage presenting in an extragonadal location. These tumors are seldom identified in the gastrointestinal tract. There is increased risk of extragonadal germ cell tumors (EGCT) in men with Klinefelter syndrome (KS). We report a rare case of a 37-year-old male with KS and EGCT discovered in the duodenum and pelvis. After treatment with Bleomycin-Etoposide-Cisplatin (BEP), he developed growing teratoma syndrome (GTS) and myelodysplasia. Despite surgical excision of the pelvic growing teratoma, he unfortunately died secondary to complications of severe bone marrow suppression.
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spelling doaj.art-9a4aadb02b8545b8bdf12d651b3ea46d2022-12-21T19:47:38ZengElsevierUrology Case Reports2214-44202017-01-0110C1310.1016/j.eucr.2016.09.006Klinefelter Syndrome with Poor Risk Extragonadal Germ Cell TumorJeremy A. KonheimJonathan A. IsraelScott E. DelacroixGerm cell tumors are the most common malignancy in men aged 15-35 years old, with a small percentage presenting in an extragonadal location. These tumors are seldom identified in the gastrointestinal tract. There is increased risk of extragonadal germ cell tumors (EGCT) in men with Klinefelter syndrome (KS). We report a rare case of a 37-year-old male with KS and EGCT discovered in the duodenum and pelvis. After treatment with Bleomycin-Etoposide-Cisplatin (BEP), he developed growing teratoma syndrome (GTS) and myelodysplasia. Despite surgical excision of the pelvic growing teratoma, he unfortunately died secondary to complications of severe bone marrow suppression.http://www.sciencedirect.com/science/article/pii/S2214442016301127Extragonadal germ cell tumorKlinefelter syndromeGrowing teratoma syndromeMyelodysplasia
spellingShingle Jeremy A. Konheim
Jonathan A. Israel
Scott E. Delacroix
Klinefelter Syndrome with Poor Risk Extragonadal Germ Cell Tumor
Urology Case Reports
Extragonadal germ cell tumor
Klinefelter syndrome
Growing teratoma syndrome
Myelodysplasia
title Klinefelter Syndrome with Poor Risk Extragonadal Germ Cell Tumor
title_full Klinefelter Syndrome with Poor Risk Extragonadal Germ Cell Tumor
title_fullStr Klinefelter Syndrome with Poor Risk Extragonadal Germ Cell Tumor
title_full_unstemmed Klinefelter Syndrome with Poor Risk Extragonadal Germ Cell Tumor
title_short Klinefelter Syndrome with Poor Risk Extragonadal Germ Cell Tumor
title_sort klinefelter syndrome with poor risk extragonadal germ cell tumor
topic Extragonadal germ cell tumor
Klinefelter syndrome
Growing teratoma syndrome
Myelodysplasia
url http://www.sciencedirect.com/science/article/pii/S2214442016301127
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AT scottedelacroix klinefeltersyndromewithpoorriskextragonadalgermcelltumor