A Rare Case of Renal Angiomyolipoma and Polycystic Kidney Disease in a Patient with Tuberous Sclerosis.

Shah, Rohan; Venkata Renuka, Inuganti; Gundapaneni, Tejasri; Shah, Haritha

Shah, Rohan; Venkata Renuka, Inuganti; Gundapaneni, Tejasri; Shah, Haritha.

Afiliación

Shah R; Pathology, NRI Medical College, Guntur, IND.
Venkata Renuka I; Pathology, NRI Medical College, Guntur, IND.
Gundapaneni T; Pathology, NRI Medical College, Guntur, IND.
Shah H; Pathology, NRI Medical College, Guntur, IND.

Cureus ; 16(6): e63031, 2024 Jun.

Article en En | MEDLINE | ID: mdl-39050299

ABSTRACT

ABSTRACT

Renal angiomyolipoma (AML) is a rare benign tumor that follows an autosomal dominant inheritance pattern. Its association with polycystic kidney disease is uncommon, with only a handful of cases documented in the literature. The growth of lesions to a significant size may lead to life-threatening complications. We report a case of a 32-year-old female who presented with a palpable mass and bilateral flank pain. Following clinical assessment and CT examination, the patient underwent a left radical nephrectomy. The resected mass measured 9.3 x 8.2 x 7.5 cm, and the subsequent histopathological examination confirmed the diagnosis as renal AML.

Palabras clave

kidney disease; multicystic renal mass; polycystic kidney disease (pkd); renal angiomyolipoma; s: tuberous sclerosis

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cureus Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

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