Presacral Ganglioneuroma: Diagnostic Considerations and Therapeutic Strategy

Presacral ganglioneuroma is an extremely rare tumor of neural crest origin. To the best of our knowledge, less than 20 cases have been reported previously. The present study reports on a presacral ganglioneuroma, 10.5 × 8 × 4 cm in size, that was found incidentally in a 35-year-old man with prior hi...

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Main Authors: Konstantinos Vardas, Dimitrios Manganas, Georgios Papadimitriou, Vasileios Vougas, Athanasios Bakalis, Maria Chantziara, Dimitrios Exarhos, Spiros Drakopoulos
Format: Article
Language:English
Published: Karger Publishers 2013-11-01
Series:Case Reports in Oncology
Subjects:
Online Access:http://www.karger.com/Article/FullText/356707
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spelling doaj-50a2a14afc9c44a1acd95d22d6bdfcdb2020-11-24T21:00:27ZengKarger PublishersCase Reports in Oncology1662-65752013-11-016356156810.1159/000356707356707Presacral Ganglioneuroma: Diagnostic Considerations and Therapeutic StrategyKonstantinos VardasDimitrios ManganasGeorgios PapadimitriouVasileios VougasAthanasios BakalisMaria ChantziaraDimitrios ExarhosSpiros DrakopoulosPresacral ganglioneuroma is an extremely rare tumor of neural crest origin. To the best of our knowledge, less than 20 cases have been reported previously. The present study reports on a presacral ganglioneuroma, 10.5 × 8 × 4 cm in size, that was found incidentally in a 35-year-old man with prior history of diverticulitis. He was admitted to our hospital due to lower left abdominal pain. Abdominal computed tomography and magnetic resonance imaging confirmed the extension of the lesion from the S2 level to the coccyx. The mass had low signal intensity on T1-weighted images and heterogeneous high signal intensity on T2-weighted images with no intraspinal or rectal extension. T2-weighted images demonstrated a compartmentalized solid tumor with cystic components. Complete tumor resection with free surgical margins was achieved using an abdominal approach. The patient remains asymptomatic 2 years after surgery. We emphasize on clinical features, radiologic appearance and surgical treatment of this rare entity. The clinical and pathologic features of previously reported studies are also briefly reviewed.http://www.karger.com/Article/FullText/356707GanglioneuromaPresacral ganglioneuromaRetrorectal tumors
collection DOAJ
language English
format Article
sources DOAJ
author Konstantinos Vardas
Dimitrios Manganas
Georgios Papadimitriou
Vasileios Vougas
Athanasios Bakalis
Maria Chantziara
Dimitrios Exarhos
Spiros Drakopoulos
spellingShingle Konstantinos Vardas
Dimitrios Manganas
Georgios Papadimitriou
Vasileios Vougas
Athanasios Bakalis
Maria Chantziara
Dimitrios Exarhos
Spiros Drakopoulos
Presacral Ganglioneuroma: Diagnostic Considerations and Therapeutic Strategy
Case Reports in Oncology
Ganglioneuroma
Presacral ganglioneuroma
Retrorectal tumors
author_facet Konstantinos Vardas
Dimitrios Manganas
Georgios Papadimitriou
Vasileios Vougas
Athanasios Bakalis
Maria Chantziara
Dimitrios Exarhos
Spiros Drakopoulos
author_sort Konstantinos Vardas
title Presacral Ganglioneuroma: Diagnostic Considerations and Therapeutic Strategy
title_short Presacral Ganglioneuroma: Diagnostic Considerations and Therapeutic Strategy
title_full Presacral Ganglioneuroma: Diagnostic Considerations and Therapeutic Strategy
title_fullStr Presacral Ganglioneuroma: Diagnostic Considerations and Therapeutic Strategy
title_full_unstemmed Presacral Ganglioneuroma: Diagnostic Considerations and Therapeutic Strategy
title_sort presacral ganglioneuroma: diagnostic considerations and therapeutic strategy
publisher Karger Publishers
series Case Reports in Oncology
issn 1662-6575
publishDate 2013-11-01
description Presacral ganglioneuroma is an extremely rare tumor of neural crest origin. To the best of our knowledge, less than 20 cases have been reported previously. The present study reports on a presacral ganglioneuroma, 10.5 × 8 × 4 cm in size, that was found incidentally in a 35-year-old man with prior history of diverticulitis. He was admitted to our hospital due to lower left abdominal pain. Abdominal computed tomography and magnetic resonance imaging confirmed the extension of the lesion from the S2 level to the coccyx. The mass had low signal intensity on T1-weighted images and heterogeneous high signal intensity on T2-weighted images with no intraspinal or rectal extension. T2-weighted images demonstrated a compartmentalized solid tumor with cystic components. Complete tumor resection with free surgical margins was achieved using an abdominal approach. The patient remains asymptomatic 2 years after surgery. We emphasize on clinical features, radiologic appearance and surgical treatment of this rare entity. The clinical and pathologic features of previously reported studies are also briefly reviewed.
topic Ganglioneuroma
Presacral ganglioneuroma
Retrorectal tumors
url http://www.karger.com/Article/FullText/356707
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