Abstract
Pediatric peritoneal sarcomatosis is an exceedingly rare entity with unknown incidence. Within these tumors, primary peritoneal rhabdomyosarcoma constitutes a small fraction. Majority of them are probably treated inadequately and have dismal outcomes. A favorable subset exists where aggressive treatment in the form of cytoreductive surgery supplemented by hyperthermic intraperitoneal chemotherapy in the multimodal setting can be attempted. We present a case of primary peritoneal embryonal rhabdomyosarcoma in a 2-year-old child who was treated with systemic chemotherapy, cytoreductive surgery, and hyperthermic intraperitoneal chemotherapy while avoiding radiation, with its evidence and rationale.
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All data was retrieved from electronic medical records of the hospital.
Abbreviations
- CECT:
-
Contrast-enhanced computerized tomography
- CRS:
-
Cytoreductive surgery
- DFS:
-
Disease-free survival
- DSRCT:
-
Desmoplastic small round cell tumor
- FDG:
-
18 Fluorodeoxyglucose
- HIPEC:
-
Hyperthermic intraperitoneal chemotherapy
- OS:
-
Overall survival
- PCI:
-
Peritoneal carcinomatosis index
- PET:
-
Positron emission tomography
- RMS:
-
Rhabdomyosarcoma
- SUVmax:
-
Maximum standardized uptake value
- WAP-RT:
-
Whole abdominopelvic radiation therapy
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We thank the patient’s family for consenting to publish their case details.
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Mufaddal Kazi: Designed and wrote the manuscript; performed surgery
Sajid S. Qureshi: Designed and critically reviewed the manuscript; performed surgery
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All procedures followed were in accordance with the ethical standards of the responsible committee (institutional and national). Ethics committee approval was not required for the case report. Consent for publication from the patient was obtained.
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The authors declare no competing interests.
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Kazi, M., Qureshi, S.S. Primary Peritoneal Rhabdomyosarcomatosis in a 2-Year-Old Child Treated with Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy — Case Report and Review of Literature. Indian J Surg Oncol 12 (Suppl 2), 322–326 (2021). https://doi.org/10.1007/s13193-021-01351-3
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DOI: https://doi.org/10.1007/s13193-021-01351-3