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Wilms Tumor with Mulibrey Nanism: A Case Report and Review of Literature
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  • K Upasana,
  • Dhwanee Thakkar,
  • Dheeraj Gautam,
  • Manvinder Sachdev,
  • Anjali Yadav,
  • Rohit Kapoor,
  • Veena Raghunathan,
  • Manider Dhaliwal,
  • Katikeya Bhargava,
  • Sandhya Nair,
  • Jaiprakash Sharma,
  • Neha Rastogi,
  • Satya Yadav
K Upasana
Medanta The Medicity

Corresponding Author:[email protected]

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Dhwanee Thakkar
Fortis Memorial Research Institute
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Dheeraj Gautam
Medanta The Medicity
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Manvinder Sachdev
Medanta The Medicity
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Anjali Yadav
Medanta The Medicity
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Rohit Kapoor
Medanta The Medicity
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Veena Raghunathan
Medanta The Medicity
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Manider Dhaliwal
Medanta The Medicity
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Katikeya Bhargava
Medanta The Medicity
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Sandhya Nair
MedGenome Labs Ltd.
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Jaiprakash Sharma
Medanta The Medicity
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Neha Rastogi
Medanta The Medicity
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Satya Yadav
Medanta The Medicity
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Abstract

Mulibrey-Nanism (Muscle-liver-brain-eye nanism= dwarfism) is a rare syndrome. The underlying TRIM37 mutation predisposes these children to develop tumors frequently. Wilms tumor has been reported to be associated with this syndrome. Here we report a 2-year-old boy with Wilms tumor and Mulibrey-Nanism and review the published similar cases. Our patient had associated atrial septal defect, atrial flutter and an episode of cardiac arrest along with other features of Mulibrey Nanism. We managed him successfully with chemotherapy and surgery. A total of 14 cases (including present case) of Wilms tumor have been reported in Mulibrey-Nanism. Longest survivor has been 15-year-old.
26 Jul 2021Published in Cancer Reports. 10.1002/cnr2.1512