LUMBOSACRAL WILMS' TUMOR AS A COMPONENT OF IMMATURE TERATOMA ASSOCIATED WITH SPINAL DYSRAPHISM—A RARE CASE AND SHORT LITERATURE REVIEW

2009 ◽  
Vol 28 (5) ◽  
pp. 201-208 ◽  
Author(s):  
Mehar Chand Sharma ◽  
Deepali Jain ◽  
Chitra Sarkar ◽  
Veereshwar Bhatnagar ◽  
Arvind Rishi ◽  
...  
Keyword(s):  
Literature Review ◽  
Rare Case ◽  
Wilms Tumor ◽  
Spinal Dysraphism ◽  
Immature Teratoma

LUMBOSACRAL WILMS' TUMOR AS A COMPONENT OF IMMATURE TERATOMA ASSOCIATED WITH SPINAL DYSRAPHISM—A RARE CASE AND SHORT LITERATURE REVIEW

2009 ◽  
Vol 28 (5) ◽  
pp. 201-208 ◽  
Author(s):  
Mehar Chand Sharma ◽  
Deepali Jain ◽  
Chitra Sarkar ◽  
Veereshwar Bhatnagar ◽  
Arvind Rishi ◽  
...  
Keyword(s):  
Literature Review ◽  
Rare Case ◽  
Wilms Tumor ◽  
Spinal Dysraphism ◽  
Immature Teratoma

scholarly journals An unusual Wilms tumor with urethral recurrence: rare case report and literature review

2015 ◽  
Vol 2 (4) ◽  
Author(s):  
Elizaveta Chernetsova ◽  
Ahmed Nasr ◽  
Luis Gerra ◽  
Bilaal Kabir ◽  
Marie JeongMin Kim ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Case ◽  
Wilms Tumor ◽  
Rare Case Report ◽  
Urethral Recurrence

scholarly journals Immature teratoma of kidney in a 5-month-old child

2013 ◽  
Vol 3 (5) ◽  
pp. 425-427
Author(s):  
RC Adhikari ◽  
G Sayami
Keyword(s):  
Preoperative Diagnosis ◽  
Rare Case ◽  
Wilms Tumor ◽  
Histopathological Examination ◽  
Abdominal Mass ◽  
Left Kidney ◽  
Immature Teratoma ◽  
Female Infant ◽  
Imaging Findings

We report a rare case of immature renal teratoma in a 5-month-old female infant. The patient presented with abdominal mass, which was found to arise from the left kidney. The preoperative diagnosis of Wilms’ tumor was based on clinical and imaging findings. The patient was managed with nephrectomy and had normal recovery. The histopathological examination of nephrectomy specimen revealed grade 2 immature teratoma. Journal of Pathology of Nepal (2013) Vol. 3, No.1, Issue 5, 425-527 DOI: http://dx.doi.org/10.3126/jpn.v3i5.7875

Popliteal nodal metastasis from squamous cell cancer of the foot. Case report and literature review

2019 ◽  
pp. 1-2
Keyword(s):  
Case Report ◽  
Lymph Node ◽  
Literature Review ◽  
Squamous Cell ◽  
Rare Case ◽  
Squamous Cell Cancer ◽  
Cell Cancer ◽  
Nodal Metastasis ◽  
Regional Disease ◽  
The Right

We report a very rare case of squamous cell cancer of the right foot which had metastasize to the ipsilateral popliteal lymph node after initial diagnosis and treatment for the loco-regional disease.

A rare case of heterotopic pregnancy after a single embryo transfer: A case report and literature review

2021 ◽  
Author(s):  
Satoshi Hosoya ◽  
Yuta Kasahara ◽  
Hiromi Komazaki ◽  
Hiroshi Kishi ◽  
Hirokuni Takano ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Embryo Transfer ◽  
Rare Case ◽  
Single Embryo Transfer ◽  
Heterotopic Pregnancy

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

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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