We report a case of congenital retroperitoneal trointestinal toxicity. The treatment resulted in fibrosarcoma presenting in a 17-day-old male clinical remission after 9 months of follow-up. in which surgical tumor debulking was followed A review of the current literature revealed the by chemotherapy
Retroperitoneal paraganglioma and systemic amyloidosis. A case report
✍ Scribed by Celestino Rey; José C. Escribano; M. Teresa Vidal
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 461 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0008-543X
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✦ Synopsis
The case of a 50-year-old woman with a retroperitoneal paraganglioma and nephrotic syndrome is presented. After the tumor was removed deposits of amyloid material were observed in the paraganglioma, kidneys, and liver. There was no thrombosis of the renal vein. The clinical picture (fever and nephrotic syndrome) was similar to that of patients with amyloidosis associated with neoplasms. The nephrotic syndrome disappeared 8 months after the operation. The patient has not had fever or nephrotic manifestations over the past 4 years and is asymptomatic at the present time. We believe this to be the first reported case of paraganglioma associated with amyloidosis. Nor have we found any references to clinical and biological remission of the nephrotic syndrome following surgical removal of the concomitant neoplasm.
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## LETTERS restriction, prednisone 100 mg daily, and Dilantin 300 mg daily. Urine output increased from 600 cc to 1,800 cc daily. The serum sodium rose to 142 mEq/liter. His mental status improved dramatically, and there was no further seizure activity. The subsequent course was complicated by a p