Literature DB >> 21119287

Neurofibroma of kidney: an uncommon neoplasm and diagnostic dilemma with solitary fibrous tumor.

Santosh Kumar Mondal1, Mamata Guha Mallick, Ranjana Bandyopadhyay, Palash Kumar Mondal.   

Abstract

Neurofibroma of kidney is an extremely rare tumor. To our knowledge, only five such cases have been reported worldwide till date. Here, we report a solitary neurofibroma of right kidney in a 54-year-old woman. Radiological investigations (ultrasonography and computed tomography) detected a solid mass in the upper pole of right kidney and clinicoradiologically renal cell carcinoma was suspected. A radical nephrectomy was performed under diagnosis of cancer. Microscopically, tumor consisted of benign spindle-shaped cells accompanied by fibrous tissue. Differential diagnoses of neurofibroma and solitary fibrous tumor (SFT) were made on morphological features. Immunohistochemically, the tumor cells were positive for S-100 protein, but negative for CD34 and CD99. Thus, a diagnosis of neurofibroma was established.

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Year:  2010        PMID: 21119287     DOI: 10.4103/0973-1482.73347

Source DB:  PubMed          Journal:  J Cancer Res Ther        ISSN: 1998-4138            Impact factor:   1.805


  2 in total

1.  Parapelvic solitary neurofibroma of the kidney.

Authors:  Bhupendra Pal Singh; Srinivas Arakalagud Krishnaswamy; Atin Singhai; Satyanarayan Sankhwar
Journal:  BMJ Case Rep       Date:  2015-06-10

2.  Retroperitoneal pararenal isolated neurofibroma: report of a case and review of literature.

Authors:  C Corbellini; A Vingiani; F Maffini; A Chiappa; E Bertani; B Andreoni
Journal:  Ecancermedicalscience       Date:  2012-05-15
  2 in total

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