Difference between revisions of "Renal oncocytosis"

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==General==
==General==
*Rare.
*Rare.
*May be seen in the context of [[Birt–Hogg–Dubé syndrome]] or renal failure or may be sporadic.
*May be seen in the context of [[Birt–Hogg–Dubé syndrome]] or [[chronic renal failure]] or may be sporadic.<ref name=pmid23018240/>


==Gross==
==Gross==

Revision as of 04:03, 4 December 2015

Renal oncocytosis
Diagnosis in short
LM DDx other renal tumours with eosinophilic cytoplasm
IHC characteristic of the histologic appearance - stain like oncocytoma, ChRCC and hybrid tumour
Gross multiple brown kidney nodules (bilateral or unilateral)
Site kidney - see kidney tumours

Syndromes Birt–Hogg–Dubé syndrome

Prevalence rare
Radiology multiple renal tumours
Clin. DDx metastatic disease, multifocal renal cell carcinoma

Renal oncocytosis is the presence of multiple oncocytic lesions within the kidney.[1]

General

Gross

  • Multiple (unilateral or bilateral) brown-coloured nodules.[1]

Microscopic

Features:

DDx:

IHC

See also

References

  1. 1.0 1.1 1.2 1.3 Kuroda, N.; Tanaka, A.; Ohe, C.; Mikami, S.; Nagashima, Y.; Sasaki, T.; Inoue, K.; Hes, O. et al. (Nov 2012). "Review of renal oncocytosis (multiple oncocytic lesions) with focus on clinical and pathobiological aspects.". Histol Histopathol 27 (11): 1407-12. PMID 23018240.