User:Mr. Ibrahem/Wilms' tumor

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Wilms' tumor
Other namesWilms's tumor, nephroblastoma
Cut section showing two halves of a Wilms' tumor. Note the prominent septa subdividing the sectioned surface and the protrusion of tumor into the renal pelvis, resembling sarcoma botryoides.
Pronunciation
SpecialtyOncology, urology
SymptomsBlood in the urine, abdominal mass, abdominal pain, high blood pressure[1][2]
ComplicationsSpread, Von Willebrand's disease[2]
Usual onset3 to 5 years old[2]
TypesStage I to V[1]
CausesUsually unclear[2]
Diagnostic methodMedical imaging[2]
Differential diagnosisClear cell renal sarcoma, rhabdoid renal tumor, congenital mesoblastic nephroma, renal cell cancer[2]
TreatmentSurgical removal of the kidney, chemotherapy[2]
PrognosisFive-year survival 78% to 92% depending on access to treatment[2]
Frequency650 cases per year (USA)[3]

Wilms' tumor, also known as nephroblastoma, is a type of kidney cancer that typically occurs in children.[1] Symptoms may include blood in the urine, abdominal mass, abdominal pain, or high blood pressure.[1][2] In about 5% of cases both kidneys are involved.[2] It can spread to the lungs, liver, bone, brain, or lymph nodes.[1] Other complications can include Von Willebrand's disease.[2]

The cause in most cases is unclear, though it is associated with a number of genetic changes.[2] It is rare for a person's parents to be affected.[2] About 10% of cases are associated with other birth defects, such as WAGR syndrome or Drash syndrome.[3] Diagnosis is usually by medical imaging as a biopsy may spread the disease.[2]

Treatment generally involves surgical removal of the kidney and chemotherapy.[2] The lymph nodes around the aorta are generally checked at the time of surgery for spread.[2] In more severe disease radiation therapy may be used.[2] The five year survival is 92% in the United States and 78% in the developing world.[2]

Wilms' tumor occurs in about 1 in 10,000 children less than a year old and 1 in 100,000 children less than 15 years old a year.[3] About 650 cases occur a year in the United States.[3] It is the most common type of kidney cancer in children under 15 years old and the 4th most common childhood cancer.[1][2] It occurs more commonly in Africans than East Asians.[2] It is named after Max Wilms, the German surgeon who first described it in 1899.[4][2]

References[edit]

  1. ^ a b c d e f "Wilms Tumor and Other Childhood Kidney Tumors Treatment (PDQ®)–Patient Version - National Cancer Institute". www.cancer.gov. 5 May 2006. Retrieved 25 January 2021.
  2. ^ a b c d e f g h i j k l m n o p q r s t u Leslie, SW; Sajjad, H; Murphy, PB (January 2020). "Wilms Tumor". PMID 28723033. {{cite journal}}: Cite journal requires |journal= (help)
  3. ^ a b c d "Wilms Tumor and Other Childhood Kidney Tumors Treatment (PDQ®)–Health Professional Version - National Cancer Institute". www.cancer.gov. 6 November 2020. Retrieved 25 January 2021.
  4. ^ "Max Wilms". www.whonamedit.com. Retrieved 25 January 2021.