Primary Rhabdomyosarcoma of Pancreas: An Extremely Rare Entity

The most recognized soft-tissue sarcoma in children is represented by Rhabdomyosarcoma (RMS). RMS is derived from striated muscle cells or their mesenchymal precursors, with the potential for skeletal muscle differentiation. The most frequent location sites are head and neck, pelvis and extremities....

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Published in:Türk onkoloji dergisi 2020, Vol.35 (2)
Main Author: sakhri, saida
Format: Article
Language:English
Subjects:
Abdomen
Adults
Biopsy
Case reports
Chemotherapy
Conflicts of interest
Cysts
Lymphatic system
Medical diagnosis
Medical imaging
Medical prognosis
Metastasis
Pain
Patients
Pediatrics
Rhabdomyosarcoma
Sarcoma
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description The most recognized soft-tissue sarcoma in children is represented by Rhabdomyosarcoma (RMS). RMS is derived from striated muscle cells or their mesenchymal precursors, with the potential for skeletal muscle differentiation. The most frequent location sites are head and neck, pelvis and extremities. However, the pancreatic location is an unusual circumstance. In this study, we report a case of a 20-yearold woman who was consulted for abdominal pain and severe vomiting. A suspicious pancreatic mass was revealed by radiological investigations. The biopsy with histological exam concluded to RMS of the pancreas. Further investigations showed a metastatic supra-clavicular lymph node. The patient was proposed for biliary stent and palliative chemotherapy, but unfortunately, she passed away five months years following the diagnosis of RMS. However, RMS is frequent in childhood, but the pancreatic location is extremely rare. The physician should keep in mind the primary pancreatic location of rhabdomyosarcoma in young patients.
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subjects Abdomen
Adults
Biopsy
Case reports
Chemotherapy
Conflicts of interest
Cysts
Lymphatic system
Medical diagnosis
Medical imaging
Medical prognosis
Metastasis
Pain
Patients
Pediatrics
Rhabdomyosarcoma
Sarcoma
title Primary Rhabdomyosarcoma of Pancreas: An Extremely Rare Entity
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