Prognosis of childhood abdominopelvic rhabdomyosarcoma: Case series

Introduction: Rhabdomyosarcoma, the most common malignant mesenchymal tumour in children, primarily affects the urogenitals. In Europe, the prognosis of the localised forms is excellent, whereas in sub-saharan Africa, it is reserved. This observation study aimed to report the diagnostic, therapeutic...

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Main Authors: Kokoé Agblévi Midékor Gonébo, Moufidath Sounkéré Soro, Rébécca Bonny Obro, Amenan Kan Sophie Kouassi Dria, Sigué Jean Jaurès Ouattara, Yapi Landry Aké, Nicolas Moh Ello
Format: Article
Language:English
Published: Elsevier 2023-06-01
Series:Journal of Pediatric Surgery Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2213576623000593
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author Kokoé Agblévi Midékor Gonébo
Moufidath Sounkéré Soro
Rébécca Bonny Obro
Amenan Kan Sophie Kouassi Dria
Sigué Jean Jaurès Ouattara
Yapi Landry Aké
Nicolas Moh Ello
author_facet Kokoé Agblévi Midékor Gonébo
Moufidath Sounkéré Soro
Rébécca Bonny Obro
Amenan Kan Sophie Kouassi Dria
Sigué Jean Jaurès Ouattara
Yapi Landry Aké
Nicolas Moh Ello
author_sort Kokoé Agblévi Midékor Gonébo
collection DOAJ
description Introduction: Rhabdomyosarcoma, the most common malignant mesenchymal tumour in children, primarily affects the urogenitals. In Europe, the prognosis of the localised forms is excellent, whereas in sub-saharan Africa, it is reserved. This observation study aimed to report the diagnostic, therapeutic, evolutionary, and prognostic aspects of rhabdomyosarcoma. Case presentation: This was a series of six observations in four boys and two girls, all of whom had no significant medical history. An abdominal mass in two patients and a pelvic mass in the others evolved over 10 days to 4 months. All localizations were complicated by signs of compression: urinary for the pelvic and digestive for the abdomen. CT tomography revealed urogenital localisation in four patients and abdominal localisation in one patient. A histological examination revealed embryonic rhabdomyosarcoma in all patients. Chemotherapy was neoadjuvant in five patients and postoperative in one patient. Immediate tumour resection was performed in one patient. All patients died: five during chemotherapy and one following recurrence after 1 year of remission. Conclusion: The prognosis of rhabdomyosarcomas is linked to delays in consultation, tumour size, histological type, and therapeutic difficulties. Adequate management of this condition requires multidisciplinary consultation.
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spelling doaj.art-d2fb68c2c1234a998a46a82b61a572b02023-05-11T04:23:54ZengElsevierJournal of Pediatric Surgery Case Reports2213-57662023-06-0193102633Prognosis of childhood abdominopelvic rhabdomyosarcoma: Case seriesKokoé Agblévi Midékor Gonébo0Moufidath Sounkéré Soro1Rébécca Bonny Obro2Amenan Kan Sophie Kouassi Dria3Sigué Jean Jaurès Ouattara4Yapi Landry Aké5Nicolas Moh Ello6Corresponding author. Pediatric Surgery Department of Cocody University Hospital, 22 BP 1178 Abidjan 22, Abidjan, Cote d’Ivoire.; Pediatric Surgery Department of Cocody University Hospital, Abidjan, Cote d’IvoirePediatric Surgery Department of Cocody University Hospital, Abidjan, Cote d’IvoirePediatric Surgery Department of Cocody University Hospital, Abidjan, Cote d’IvoirePediatric Surgery Department of Cocody University Hospital, Abidjan, Cote d’IvoirePediatric Surgery Department of Cocody University Hospital, Abidjan, Cote d’IvoirePediatric Surgery Department of Cocody University Hospital, Abidjan, Cote d’IvoirePediatric Surgery Department of Cocody University Hospital, Abidjan, Cote d’IvoireIntroduction: Rhabdomyosarcoma, the most common malignant mesenchymal tumour in children, primarily affects the urogenitals. In Europe, the prognosis of the localised forms is excellent, whereas in sub-saharan Africa, it is reserved. This observation study aimed to report the diagnostic, therapeutic, evolutionary, and prognostic aspects of rhabdomyosarcoma. Case presentation: This was a series of six observations in four boys and two girls, all of whom had no significant medical history. An abdominal mass in two patients and a pelvic mass in the others evolved over 10 days to 4 months. All localizations were complicated by signs of compression: urinary for the pelvic and digestive for the abdomen. CT tomography revealed urogenital localisation in four patients and abdominal localisation in one patient. A histological examination revealed embryonic rhabdomyosarcoma in all patients. Chemotherapy was neoadjuvant in five patients and postoperative in one patient. Immediate tumour resection was performed in one patient. All patients died: five during chemotherapy and one following recurrence after 1 year of remission. Conclusion: The prognosis of rhabdomyosarcomas is linked to delays in consultation, tumour size, histological type, and therapeutic difficulties. Adequate management of this condition requires multidisciplinary consultation.http://www.sciencedirect.com/science/article/pii/S2213576623000593Case seriesChildPelvisPrognosisRhabdomyosarcoma
spellingShingle Kokoé Agblévi Midékor Gonébo
Moufidath Sounkéré Soro
Rébécca Bonny Obro
Amenan Kan Sophie Kouassi Dria
Sigué Jean Jaurès Ouattara
Yapi Landry Aké
Nicolas Moh Ello
Prognosis of childhood abdominopelvic rhabdomyosarcoma: Case series
Journal of Pediatric Surgery Case Reports
Case series
Child
Pelvis
Prognosis
Rhabdomyosarcoma
title Prognosis of childhood abdominopelvic rhabdomyosarcoma: Case series
title_full Prognosis of childhood abdominopelvic rhabdomyosarcoma: Case series
title_fullStr Prognosis of childhood abdominopelvic rhabdomyosarcoma: Case series
title_full_unstemmed Prognosis of childhood abdominopelvic rhabdomyosarcoma: Case series
title_short Prognosis of childhood abdominopelvic rhabdomyosarcoma: Case series
title_sort prognosis of childhood abdominopelvic rhabdomyosarcoma case series
topic Case series
Child
Pelvis
Prognosis
Rhabdomyosarcoma
url http://www.sciencedirect.com/science/article/pii/S2213576623000593
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