Maturation of Pulmonary Metastases of Wilms' Tumor after Therapy: A Case Report

Abstract Background Repeat pulmonary metastasectomy (PM) considerably improves the prognosis of patients with pulmonary metastases of osteosarcoma. Reports have demonstrated a significantly improved prognosis in patients who have undergone repeat metastasectomy for osteosarcoma; however, there have been no reports with more than six metastasectomies. Herein, we describe the long-term survival of a patient following resection of multiple tumors and other treatments for metastatic osteosarcoma. Case presentation A 28-year-old woman underwent extensive resection and postoperative adjuvant chemotherapy for right tibial sarcoma. Over the years, she developed repeated pulmonary metastases. First, 116 metastases were removed from the bilateral lungs. After that, multiple PMs of approximately 250 tumors and other treatments for deep metastatic lesions were performed. The patient died of the underlying disease 24 years after the primary surgery. Conclusions This case report demonstrates the long-term survival benefit of a multidisciplinary treatment centered on multiple metastasectomies.

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Is it always Wilms’ tumor? Localized cystic disease of the kidney in an infant. An extremely rare case report and review of the literature

Pediatric Reports ◽

10.4081/pr.2020.8483 ◽

2020 ◽

Vol 12 (1) ◽

Author(s):

Christos Kaselas ◽

Charikleia Demiri ◽

Vasilios Mouravas ◽

Eleni Koutra ◽

Kleanthis Anastasiadis ◽

...

Keyword(s):

Case Report ◽

Rare Case ◽

Wilms Tumor ◽

Pediatric Population ◽

Benign Disease ◽

Cystic Disease ◽

Proper Treatment ◽

Review Of The Literature ◽

Rare Case Report ◽

Renal Malignancies

Localized Cystic Disease of the Kidney (LCDK) is an extremely rare benign disease in pediatric population. Although its management is conservative and generally requires no treatment, the unfamiliarity with the disease can expose such patients to misdiagnosis as renal malignancies or uncertainty for proper treatment. We report such a case in an infant and review the current literature.

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Renal Sparing Surgery Using Focus Ultracision Harmonic Scalpel in Patients with Bilateral Wilms’ Tumor: Case Report

Balkan Medical Journal ◽

10.5152/balkanmedj.2013.7589 ◽

2013 ◽

Vol 30 (3) ◽

pp. 318-320 ◽

Cited By ~ 1

Author(s):

Murat Alkan ◽

Cemal Parlakgumus ◽

Serdar Hilmi Iskit ◽

Recep Tuncer ◽

Hasan Okur ◽

...

Keyword(s):

Case Report ◽

Harmonic Scalpel ◽

Wilms Tumor ◽

Bilateral Wilms Tumor

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Congenital Bilateral Wilms Tumor: A Case Report

Urology ◽

10.1016/j.urology.2021.08.011 ◽

2021 ◽

Author(s):

Deguang Meng ◽

Xiaofeng Chang ◽

Qinghua Ren ◽

Jiatong Xu ◽

Huanmin Wang

Keyword(s):

Case Report ◽

Wilms Tumor ◽

Bilateral Wilms Tumor

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Malignant Rhabdoid Tumor of the Lung in the Young Adult: A Case Report

Case Reports in Pulmonology ◽

10.1155/2011/323584 ◽

2011 ◽

Vol 2011 ◽

pp. 1-4 ◽

Cited By ~ 1

Author(s):

Adel Attia ◽

Moosa Suleman ◽

Hesham Mosleh

Keyword(s):

Case Report ◽

Young Adult ◽

Pediatric Oncology ◽

Wilms Tumor ◽

Rhabdoid Tumor ◽

Malignant Rhabdoid Tumor

Malignant rhabdoid tumor (MRT) is one of the most aggressive and lethal malignancies in pediatric oncology. Malignant rhabdoid tumor was initially described in 1978 as a rhabdomyosarcomatoid variant of a Wilms tumor because of its occurrence in the kidney and because of the resemblance of its cells to rhabdomyoblasts. The absence of muscular differentiation led Haas and colleagues to coin the term rhabdoid tumor of the kidney in 1981, Haas et al..

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Early Detection of Wilms' Tumor in a Child with Hemihypertnophy and Ovarian Cysts

PEDIATRICS ◽

10.1542/peds.70.1.135 ◽

1982 ◽

Vol 70 (1) ◽

pp. 135-136

Author(s):

Deborah Tolchin ◽

Mordecai Koenigsberg ◽

Maria Santorineou

Keyword(s):

Case Report ◽

Early Detection ◽

Ovarian Cyst ◽

Wilms Tumor ◽

Present Report ◽

Ovarian Cysts ◽

Term Pregnancy ◽

Intravenous Pyelogram ◽

Routine Examination ◽

Bilateral Wilms Tumor

There have been many reports of the association between hemihypertrophy and intraabdominal masses, including Wilms' tumor, hepatoma, and adrenal cortical neoplasias.1 The present report describes a patient with segmental hemihypertrophy, multiple ovarian cysts, and bilateral Wilms' tumor and suggests a screening regimen for patients with hemihypertrophy. CASE REPORT The patient was a 9 lb 14 oz product of a term pregnancy, who was well until a mass filling the entire right side of the abdomen was discovered on routine examination at 4 months of age. Intravenous pyelogram (IVP) confirmed a large prerenal mass which on ultrasound was felt to be an ovarian cyst.

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Isolated central nervous system metastasis in pediatric Wilms' tumor: A case report and review of literature

Urology Case Reports ◽

10.1016/j.eucr.2018.09.001 ◽

2018 ◽

Vol 21 ◽

pp. 78-80

Author(s):

Mehdi Borni ◽

Brahim Kammoun ◽

Fatma Kolsi ◽

Anis Abdelhedi ◽

Mohamed Zaher Boudawara

Keyword(s):

Central Nervous System ◽

Nervous System ◽

Case Report ◽

Wilms Tumor ◽

Review Of Literature ◽

Central Nervous System Metastasis

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Pediatric Anastomosing Hemangioma: Case Report and Review of Renal Vascular Tumors in Children

Pediatric and Developmental Pathology ◽

10.1177/1093526618809230 ◽

2018 ◽

Vol 22 (3) ◽

pp. 269-275 ◽

Cited By ~ 1

Author(s):

Alvin B Caballes ◽

Agustina D Abelardo ◽

Miguel J Farolan ◽

Januario Antonio D Veloso

Keyword(s):

Case Report ◽

Pediatric Patients ◽

Wilms Tumor ◽

Vascular Lesion ◽

Renal Tumors ◽

Vascular Tumors ◽

Malignant Neoplasms ◽

Therapeutic Implications ◽

Renal Vascular ◽

Anastomosing Hemangioma

The case involves a 10-year-old child who underwent a left radical nephrectomy for what was believed to be a Wilms’ tumor. Histopath examination indicated a benign vascular lesion, subsequently determined to be an anastomosing hemangioma of the kidney. A comparison with the previously cited pediatric patients with renal vascular tumors is provided, and the inconsistent diagnostic terminologies for these conditions are highlighted. The therapeutic implications of these predominantly benign renal tumors, in the context of the much more frequently encountered malignant neoplasms in children, are additionally discussed.

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