SavedAdd your journal

Journals / The Journal of Pediatric Research / 2022 / Cilt: 9 - Sayı: 2

An Astonishing Extrarenal Wilms Localisation; Spinal Cord

Ayşe Gülnur TOKUÇ
Nurşah EKER
Burcu Tufan TAŞ
Süheyla UYAR BOZKURT
Mustafa SAKAR
Seda ARAS
Kadriye Ebru AKAR
Pages
188–191
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Here, we report on a case with immature renal cells located in the lumber spinal cord associated with spinal dysraphism and the development of Wilms’ tumour there after one year.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Wilms’ tumour is a renal tumour mostly seen during the first 5 years of life and it accounts for 95% of renal malignancies during childhood.
📊
Key Findings & Data:The estimated rate of nephroblastoma outside the kidneys is approximately 0.5 to 1% of Wilms’ tumour cases.
💡
Conclusion & Impact:Here, we report on a case with immature renal cells located in the lumber spinal cord associated with spinal dysraphism and the development of Wilms’ tumour there after one year.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Wilms’ tumour is a renal tumour mostly seen during the first 5 years of life and it accounts for 95% of renal malignancies during childhood. Its origin is primitive metanephric cells and, very rarely, it may occur in places other than the kidneys. The estimated rate of nephroblastoma outside the kidneys is approximately 0.5 to 1% of Wilms’ tumour cases. In this article, we report on a 3-year-old female patient who first presented with spinal dysraphism and a mass in the lumbar spinal cord with a histopathological diagnosis of nephrogenic rest, and after one year, a Wilms tumour arose in this location. This is a very rare extrarenal Wilms’ tumour location. Here, we report on a case with immature renal cells located in the lumber spinal cord associated with spinal dysraphism and the development of Wilms’ tumour there after one year.

🔖

Cite This Article

TOKUÇ, A. G., EKER, N., TAŞ, B. T., BOZKURT, S. U., SAKAR, M., ARAS, S., AKAR, K. E. (2022). An Astonishing Extrarenal Wilms Localisation; Spinal Cord. The Journal of Pediatric Research, Cilt: 9 - Sayı: 2, 188–191. https://ajindex.com/articles/407372

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (17)

  1. Moyson F, Maurus-Desmarez R, Gompel C. [Mediastinal Wilms’ tumor?]. Acta Chir Belg 1961; Suppl 2:118-28
  2. Armanda V, Culić S, Pogorelić Z, Kuljiš D, Budimir D, Kuzmić- Prusac I. Rare localization of extrarenal nephroblastoma in 1-month-old female infant. J Pediatr Urol 2012; 8:e43-5
  3. Song JS, Kim IK, Kim YM, Khang SK, Kim KR, Lee Y. Extrarenal teratoid Wilms’ tumor: two cases in unusual locations, one associated with elevated serum AFP. Pathol Int 2010; 60:35-41
  4. Wu Y, Zhu X, Wang X, Wang H, Cao X, Wang J. Extrarenal nephroblastomatosis in children: a report of two cases. BMC Pediatr 2014; 14:255
  5. Andrews PE, Kelalis PP, Haase GM. Extrarenal Wilms’ tumor: results of the National Wilms’ Tumor Study. J Pediatr Surg 1992; 27:1181-4
  6. Mickle JP, McLennan JE. Malignant teratoma arising within a lipomeningocele. Case report. J Neurosurg 1975; 43:761-3
  7. Sharma MC, Jain D, Sarkar C, et al. Lumbosacral Wilms’ tumor as a component of immature teratoma associated with spinal dysraphism--a rare case and short literature review. Fetal Pediatr Pathol 2009; 28:201-8
  8. Song JS, Kim IK, Kim YM, Khang SK, Kim KR, Lee Y. Extrarenal teratoid Wilms’ tumor: two cases in unusual locations, one associated with elevated serum AFP. Pathol Int 2010; 60:35-41
  9. Tebbi K, Ragab AH, Ternberg JL, Vietti TJ. An extrarenal Wilms’ tumor arising from a sacrococcygeal teratoma. Clin Pediatr (Phila) 1974; 13:1019-21
  10. Sharma MC, Aggarwal M, Ralte AM, et al. Clinicopathological study of spinal teratomas. A series of 10 case. J Neurosurg Sci 2003; 47:95-100
  11. Posalaky Z, Drake RM, Mawk JR, et al. Ectopic immature renal tissue over the dorsum of lumbar and sacral area in two infants. Pediatrics 1982; 69:336-9
  12. Fahner JB, Switzer R, Freyer DR, Mann JD, Mann RJ. Extrarenal Wilms’ tumor. Unusual presentation in the lumbosacral region. Am J Pediatr Hematol Oncol 1993; 15:117-9
  13. Ratajczak MZ, Schneider G, Sellers ZP, Kucia M, Kakar SS. The embryonic rest hypothesis of cancer development: an old XIX century theory revisited. J Cancer Stem Cell Res 2014; 2:e1001
  14. Sell S. On the stem cell origin of cancer. Am J Pathol 2010; 176:2584-494
  15. Fernbach SK, Naidich TP, McLone DG, Leestma JE. Computed tomography of primary intrathecal Wilms tumor with diastematomyelia. J Comput Assist Tomogr 1984; 8:523-8
  16. Grobstein C. Inductive tissue interaction in development. Adv Cancer Res 1956; 4:187-236
  17. Deshpande AV, Gawali JS, Sanghani HH, Shenoy AS, Patankar JZ, Borw