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Adrenal pheochromocytoma: Keys to radiologic diagnosis.
Corral de la Calle, M A; Encinas de la Iglesia, J; Fernández-Pérez, G C; Repollés Cobaleda, M; Fraino, A.
Afiliación
  • Corral de la Calle MA; Servicio de Radiodiagnóstico, Complejo Asistencial de Ávila, Ávila, Spain. Electronic address: migcorral@gmail.com.
  • Encinas de la Iglesia J; Servicio de Radiodiagnóstico, Complejo Asistencial de Salamanca, Salamanca, Spain.
  • Fernández-Pérez GC; Centro Radiológico Grupo Recoletas, Valladolid, Spain.
  • Repollés Cobaleda M; Servicio de Radiodiagnóstico, Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
  • Fraino A; Servicio de Radiodiagnóstico, Complejo Asistencial de Ávila, Ávila, Spain.
Radiologia (Engl Ed) ; 64(4): 348-367, 2022.
Article en En | MEDLINE | ID: mdl-36030082
Pheochromocytomas are adrenal paragangliomas. Potentially malignant, these tumors have a low incidence but clear importance. They can appear in various hereditary syndromes, especially in von Hippel-Lindau syndrome, multiple endocrine neoplasia-2 (MEN2), and familial paraganglioma syndromes. In sporadic cases, underlying genetic alterations are often found, and these findings are changing our understanding of the disease. Although these tumors can manifest with a characteristic clinical presentation, in 13.1%-57.6% of cases, it is the radiologist who first suggests the diagnosis, indicating analyses for catecholamines or nuclear medicine examinations. Radiologists should suspect a pheochromocytoma on detection of a well-delimited adrenal mass with rapid, intense enhancement that typically shows cystic and hemorrhagic phenomena, high T2 signal intensity, and the absence of macroscopic or microscopic lipids. The behavior in diffusion-weighted imaging usually does not provide very useful information. Approximately one-third of lesions show late washout similar to that seen with adenomas on CT. Percutaneous puncture should be avoided to avoid the risk of unleashing a severe hypertensive crisis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Paraganglioma / Feocromocitoma / Neoplasias de las Glándulas Suprarrenales / Enfermedad de von Hippel-Lindau Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Radiologia (Engl Ed) Año: 2022 Tipo del documento: Article Pais de publicación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Paraganglioma / Feocromocitoma / Neoplasias de las Glándulas Suprarrenales / Enfermedad de von Hippel-Lindau Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Radiologia (Engl Ed) Año: 2022 Tipo del documento: Article Pais de publicación: España