MedElevator Войти в исследования
← Поиск публикаций

DOI 10.3389/fonc.2025.1543858

Медицинская библиотека · Frontiers in oncology · 2025

Case Report: A case report of the diagnosis of renal inflammatory myofibroblastic tumor.

Wu Wenjie, Liang Tiantian, Zhang Hui

Клинический случайСтатьяПеревод в очереди

Аннотация

Renal inflammatory myofibroblastic tumor is a very rare disease that primarily occurs in the renal parenchyma and may even involve the renal pelvis. This study presents a case of renal inflammatory myofibroblastic tumor with exophytic growth, whose imaging appearance resembles that of a solitary perirenal mass. A 75-year-old male patient was referred to our hospital for further treatment after a retroperitoneal lesion was discovered and suspected at another hospital. Imaging examination revealed multiple cysts in both kidneys and a lesion located anterior to a cyst at the lower pole of the left kidney. Due to the presence of the cysts, the relationship between the lesion and the kidneys was unclear. We performed multiplanar reconstruction of the tumor images and generated a temporal signal curve. Based on these imaging findings, we determined that the lesion was a benign tumor of renal origin and could be surgically removed. Finally, pathological examination confirmed the diagnosis of a renal inflammatory myofibroblastic tumor. Postoperative telephone follow-up revealed that the patient was alive, and a follow-up abdominal CT performed at the local hospital showed no recurrence.

Для цитирования: Wu Wenjie, Liang Tiantian, Zhang Hui. Case Report: A case report of the diagnosis of renal inflammatory myofibroblastic tumor.. Frontiers in oncology. 2025. DOI: 10.3389/fonc.2025.1543858.
Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.