Pheochromocytoma: A three-decade clinical experience in a multicenter study


Por: Iglesias, P, Santacruz, E, Garcia-Sancho, P, Marengo, A, Guerrero-Perez, F, Pian, H, Fajardo, C, Villabona, C and Diez, J

Publicada: 1 ene 2021
Categoría: Medicine (miscellaneous)

Resumen:
Objective: To analyze the clinical and analytical features, diagnostic tests, therapies, and outcomes of pheochromocytoma (PCC). Design and methods: A multicenter retrospective study in surgically treated patients with PCC followed in 3 Spanish tertiary referral hospitals. Results: A total of 106 patients (61 [57.5%] women, mean age 52.3 +/- 14.8 years) were evaluated. At diagnosis, PCC was symptomatic in 62% and sporadic in 83%. Patients with familial PCC were significantly younger than those with sporadic disease (40.8 +/- 14.2 years vs. 54.5 +/- 13.9 years, p<.001). Familial PCCs were more frequently associated with MEN2A (n=8). Levels of 24-h urinary fractionated metanephrines were positively related to tumor size. The maximum tumor diameter was 4.3 cm (3-6cm); 27.7% of the patients had tumors >= 6 cm. Incidental PCCs were significantly smaller than symptomatic PCCs (3.4 cm [2.4-5.0 cm] vs. 5.6cm [4.0-7.0cm], p<.001). Scintigraphy by I-123-metaiodobenzylguanidine showed a high sensitivity (81.9%). Preoperative alpha blockade with phenoxybenzamine was used in 93.6% and doxazosin in the rest. Laparoscopic surgery was used in 2/3 of the patients, with a low conversion (1.9%) to open surgery. Perioperative complications appeared in approximately 20% of patients, mainly hypertensive crisis (9.4%). Recurrent disease appeared in 10%, and malignant PCC was uncommon (6.3%). Conclusions: PCCs surgically treated in Spain are usually large, symptomatic, and sporadic tumors diagnosed around the sixth decade of life. Hereditary PCC is usually associated with MEN2A. The main type of surgical technique used is laparoscopic surgery, and the prevalence of metastatic PCC is low. (C) 2020 Elsevier Espana, S.L.U. and Sociedad Espanola de Medicina Interna (SEMI). All rights reserved.

Filiaciones:
Iglesias, P:
 Hosp Univ Ramon Y Cajal, Serv Endocrinol, Madrid, Spain

 Hosp Univ Puerta Hierro, Serv Endocrinol, Madrid, Spain

Santacruz, E:
 Hosp Univ Ramon Y Cajal, Serv Endocrinol, Madrid, Spain

Garcia-Sancho, P:
 Hosp Univ Bellvitge, Serv Endocrinol, Barcelona, Spain

Marengo, A:
 Hosp Univ Bellvitge, Serv Endocrinol, Barcelona, Spain

Guerrero-Perez, F:
 Hosp Univ Bellvitge, Serv Endocrinol, Barcelona, Spain

Pian, H:
 Hosp Univ Ramon Y Cajal, Serv Anat Patol, Madrid, Spain

:
 Hosp Univ La Ribera, Serv Endocrinol, Valencia, Spain

Villabona, C:
 Hosp Univ Bellvitge, Serv Endocrinol, Barcelona, Spain

Diez, J:
 Hosp Univ Ramon Y Cajal, Serv Endocrinol, Madrid, Spain

 Hosp Univ Puerta Hierro, Serv Endocrinol, Madrid, Spain
ISSN: 00142565





REVISTA CLINICA ESPANOLA
Editorial
EDICIONES DOYMA S A, TRAV DE GRACIA 17-21, 08021 BARCELONA, SPAIN, España
Tipo de documento: Article
Volumen: 221 Número: 1
Páginas: 18-25
WOS Id: 000604431800003
ID de PubMed: 32646754

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