Malignant rhabdoid tumor of kidney and brain in an infant

Shukla, Deepti; Pradhan, Aditya; Bhardwaj, Mukesh; Malhotra, Veena

doi:10.1007/s13312-015-0570-9

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2024

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Cited by 3 publications

(2 citation statements)

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“…It has been suggested that the origin could be from primitive cells in the renal medulla. Rhabdoid tumors of the kidney consist of cells organized in diffuse sheets, alveolar or trabecular patterns [4,5].…”

Section: Case Discussionmentioning

confidence: 99%

See 1 more Smart Citation

Rhabdoid Tumor of the Kidney in Children: A Case Report

Noor Al,

Afrah Al,

Mohamed Abdel

et al. 2024

Int J Radiol Imaging Technol

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Section: Case Discussionmentioning

confidence: 99%

“…Lack of immunohistochemical staining for SMARCB1 gene (also known as SNF5, INI-I, or BAF47) support histologic diagnosis of malignant renal rhabdoid tumors. Inactivating both copies of a gene by deletions or mutations at chromosomal location 22q11.23 cause biallelic inactivation of SMARCB1 tumor suppressor gene [4,5,7].…”

Section: Discussionmentioning

confidence: 99%

Rhabdoid Tumor of the Kidney in Children: A Case Report

Noor Al,

Afrah Al,

Mohamed Abdel

et al. 2024

Int J Radiol Imaging Technol

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Synchronous Central Nervous System Atypical Teratoid/Rhabdoid Tumor and Malignant Rhabdoid Tumor of the Kidney: Case Report of a Long-Term Survivor and Review of the Literature

et al. 2018

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Rhabdoid renal tumor: an aggressive embryonal tumor in an infant — a case report

et al. 2022

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Background Malignant rhabdoid tumor of the kidney is the most aggressive childhood renal tumor. A preoperative diagnosis is critical in order to correctly establish a therapeutic strategy and a full metastatic workup. Case presentation We report on a 3-month-old case with fever, diarrhea, and abdominal distension treated surgically with adjuvant chemotherapy. The diagnosis was confirmed postoperatively. Relapse was quick, and the child died 5 months after surgical resection. Conclusions Rhabdoid renal tumor in young age is associated with a high mortality rate even with invasive strategies. Case reports and research are critical for evaluating existing protocols and improving prognosis. Diverse clinical trials are being conducted in the hopes of improving the prognosis of rhabdoid renal tumors.

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Malignant rhabdoid tumor of kidney and brain in an infant

Abstract: Children presenting with embroynal brain tumor, should be investigated for renal tumors and vice versa.

Cited by 3 publications

References 8 publications

Rhabdoid Tumor of the Kidney in Children: A Case Report

Rhabdoid Tumor of the Kidney in Children: A Case Report

Synchronous Central Nervous System Atypical Teratoid/Rhabdoid Tumor and Malignant Rhabdoid Tumor of the Kidney: Case Report of a Long-Term Survivor and Review of the Literature

Rhabdoid renal tumor: an aggressive embryonal tumor in an infant — a case report

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