| Autor: |
Gora, Bhoopendra Singh, Singh, Suresh, Babu, Agil, Lakhera, Kamal Kishor, Patel, Pinakin, Singhal, Pranav M., Kumar, Naina, Diama, Mahesh |
| Zdroj: |
Indian Journal of Surgical Oncology; 2024 Suppl 3, Vol. 15, p456-459, 4p |
| Abstrakt: |
Renal angiomyolipoma (AML), also referred to as renal hamartoma, is a rare solid tumor without malignant characteristics. The inheritance pattern of renal AML is autosomal dominant. If the lesion grows to a large size, a series of clinical manifestations and serious complications may occur. We herein present a case of giant renal AML in a 49-year-old female patient, who presented with left-sided abdominal bloating for 1 month. Following abdominal ultrasound and computed tomography examination, the patient underwent total left nephrectomy. The resected mass was sized 18 × 15 × 11 cm. Postoperative histopathological examination confirmed the lesion as a giant renal AML. There are only few cases of giant renal AML (> 10 cm) reported in the literature to date. Due to the large size of the tumor, it is crucial to report similar cases, their diagnosis, and treatment. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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