Massive bilateral renal angiomyolipomatosis and multifocal micronodular pneumocytes hyperplasia associated with tuberous sclerosis: A case report

Abstract

Tuberous sclerosis (TS) is an autosomal-dominant disorder characterized by a variety of hamartomatous lesions in various organs. Various organ involvements can be detected with radiology: neurologic involvement (cortical tubers, subependymal nodules and white matter abnormalities), renal involvement (angiomyolipoma) and pulmonary involvement (pulmonary lymphangioleiomyomatosis, multifocal micronodular pneumocyte hyperplasia). Here, we are reporting a case of tuberous sclerosis with multiple organ involvement and massive bilateral AMLs in a 49-year-old female patient.

Imaging of Renal Angiomyolipomatosis

“…Several studies have described the radiological features of angiomyolipomatosis; for this review, we analyzed the radiological features described in several clinical cases. Imaging features of the cases of renal angiomyolipomatosis described in the literature are listed in Table 1 (40)(41)(42)(43)(44)(45)(46)(47)(48)(49).…”