Retroperitoneal fibrosis
Retroperitoneal fibrosis is a rare thingy urologists and rheumatologists dealt with.
General
- May cause obstructive uropathy.[1]
- One of the many IgG4-related systemic diseases.[2]
Treatment:
- Immunosuppression.
Microscopic
- Fibrous tissue (pink background) with inflammatory cells (plasma cells, benign lymphocytes and eosinophils).
Note:
- Entrapped adipocytes (white open spaces) are common.
Images
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A. KIDNEY, RIGHT, RADICAL NEPHRECTOMY: - SEVERE PYELONEPHRITIS, CHRONIC ACTIVE. - EXTENSIVE TOTAL SCLEROSIS OF GLOMERULI AND INTERSTITIAL FIBROSIS (END-STAGE KIDNEY). - PERIRENAL FAT WITH FOCI OF FAT NECROSIS, FIBROSIS AND A MIXED INFLAMMATORY INFILTRATE WITH PLASMA CELLS. - NEGATIVE FOR MALIGNANCY. B. SOFT TISSUE, RETROPERITONEUM, BIOPSY: - FIBROTIC SOFT TISSUE WITH A MINIMAL FOCAL LYMPHOCYTIC INFILTRATE. - NEGATIVE FOR MALIGNANCY.
See also
References
- ↑ 1.0 1.1 Rodríguez Jornet, A.; Andreu Navarro, FJ.; Orellana Fernández, R.; Ibeas López, J.; García García, M. (2009). "[Idiopathic retroperitoneal fibrosis: clinico-pathological characteristics].". Nefrologia 29 (4): 298-303. doi:10.3265/Nefrologia.2009.29.4.5344.en.full. PMID 19668300.
- ↑ Kamisawa, T.; Okamoto, A. (Jul 2008). "IgG4-related sclerosing disease.". World J Gastroenterol 14 (25): 3948-55. PMID 18609677.
- ↑ URL: http://www.mypacs.net/cases/RETROPERITONEAL-FIBROSIS-17484372.html. Accessed on: 20 October 2011.