Background: Amyloidosis is a collection of disorders characterized by the extracellular deposition of amyloid, a specialized fibrous protein, in diverse tissues, leading to functional impairments.
Case Presentation: A 70-year old Asian-Japanese female was referred to our department for further examination of her left hydronephrosis come from lower ureteral obstruction. Contrast enhanced CT and retrograde pyelo-nephrography revealed left ureteral tumor. Though ureteroscropic biopsy did not show malignant pathological findings, ureteroscopic image suspected malignant disease, thus nephroureterectomy was performed. Pathological findings revealed localized ureteral amyloidosis. Whole body examination including gastro endoscopy and cardio ultrasonography could not reveal amyloidosis except ureter. She was free from recurrence 9 months postoperatively.
Conclusion: We herein report a rare case of localized ureteral amyloidosis.
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http://dx.doi.org/10.1186/s13256-023-04138-y | DOI Listing |
J Med Case Rep
October 2023
Departments of Urology, Yokohama Municipal Citizen's Hospital, Yokohama, Japan.
Urol Case Rep
November 2023
Department of Urology, Tokyo Women's Medical University Yachiyo Medical Center, Japan.
Urol Case Rep
March 2022
Anatomic Pathology, Department of Pathology, The Ohio State University Wexner Medical Center, E411 Doan Hall, 410 W. 10th Ave, Columbus, OH, 43210, USA.
Primary amyloidosis of the ureter is a rare disease that is difficult to distinguish from urothelial carcinoma. Only 50 cases of primary ureter amyloidosis have been reported since it was first described in 1937. Of these, only five cases of ureter amyloidosis with osseous metaplasia were reported.
View Article and Find Full Text PDFUrol Case Rep
January 2022
Department of Urology, Galdakao-Usansolo Hospital, Labeaga Auzoa, 48960, Galdakao, Vizcaya, Spain.
Ureteral amyloidosis is a rare entity and of interest to urologists, hematologists, radiologists, and pathologists because it mimics urothelial cell carcinoma clinically, endoscopically and radiologically. A pre-operative ureteroscopy or surgical biopsy is required, and it is essential to exclude systemic amyloidosis. We report a male who was diagnosed with IIIA stage lymphoplasmacytic lymphoma associating systemic amyloidosis with concomitant hematuria.
View Article and Find Full Text PDFUrology
December 2020
Yale Cancer Center, Department of Medical Oncology, New Haven, CT.
Amyloid of the ureter is a rare disease with less than 25 cases reported in the literature. Despite being rare, it remains an important entity as it is typically confused with a primary neoplastic process of the urinary system. We report a case of a 68-year-old male with a history of cutaneous amyloid with late presentation of bilateral ureteral involvement.
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