Chromophobe renal cell carcinoma with sarcomatoid and heterologous osteosarcoma-like differentiation: a case report and literature review

Author:

Abuorouq Saleh12,Sahawneh Firas3,Halalsheh Omar45,Haddad Husam K6,Mekail Raed3,Alzoubi Hiba78,Alrjoub Mo’ath95,Serhan Hashem A10ORCID

Affiliation:

1. Department of Clinical Medical Sciences , Urology Division, Faculty of Medicine, , Irbid 21163 , Jordan

2. Yarmouk University , Urology Division, Faculty of Medicine, , Irbid 21163 , Jordan

3. Private Sector, Department of Urology , Irbid 21110 , Jordan

4. Department of Urology , Faculty of Medicine, , Irbid 22110 , Jordan

5. Jordan University of Science and Technology , Faculty of Medicine, , Irbid 22110 , Jordan

6. Department of Pathology and Laboratory Medicine, Ministry of Health , Amman 11118 , Jordan

7. Department of Basic Medical Sciences , Pathology Division, Faculty of Medicine, , Irbid 21163 , Jordan

8. Yarmouk University , Pathology Division, Faculty of Medicine, , Irbid 21163 , Jordan

9. Department of Pathology and Microbiology , Faculty of Medicine, , Irbid 22110 , Jordan

10. Department of Ophthalmology, Hamad Medical Corporations , Doha 3050 , Qatar

Abstract

Abstract Chromophobe renal cell carcinoma (CRCC) is a subtype of renal cell carcinoma (RCC) with a favorable prognosis. Sarcomatoid differentiation in RCC is assumed to be the outcome of the parent tumor’s dedifferentiation and associated with poorer prognosis. Sarcomatoid differentiation can be detected in CRCC as well as other subtypes, but the occurrence of divergent osteosarcoma-like components in sarcomatoid CRCC is extremely unusual. Only six cases have been previously reported in the literature, we reviewed them and presented the seventh case in a 71-year-old male who had a left kidney heterogeneous mass. The resected tumor showed a sarcoma-like spindle cell area with an adjacent osteosarcoma area producing lacy bone material and bony trabeculae in a hard area mixed with a typical CRCC. In conclusion, sarcomatoid CRCC with osteosarcomatous differentiation is a very rare tumor and should be kept in mind especially when dealing with small or frozen sections biopsies.

Funder

Qatar National Library

Publisher

Oxford University Press (OUP)

Subject

Surgery

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