Révillon Y, Daher P, Jan D, Buisson C, Bonnerot V, Martelli H, Nihoul-Fékété C
Hôpital des Enfants Malades, Paris, France.
J Pediatr Surg. 1992 Jul;27(7):910-1. doi: 10.1016/0022-3468(92)90396-o.
Pheochromocytoma is an uncommon tumor in childhood; nevertheless, 20% of all pheochromocytomas are found in the pediatric population. Fifteen children have been treated in our institution from 1962 to 1990. One percent of patients referred over the same period for investigation of high blood pressure were found to have a pheochromocytoma. The majority of patients have hypertension. It varies in intensity and is paroxysmal in about half the patients. Many pediatric cases of unilateral, bilateral, extra-adrenal, familial, and recurrent pheochromocytomas have been reported. We reviewed our 28 years experience with this tumor and concentrated on the diagnosis, the preoperative and operative management, and the occurrence of the multiple endocrine neoplasia syndromes.
嗜铬细胞瘤在儿童期是一种罕见肿瘤;然而,所有嗜铬细胞瘤中有20%见于儿科患者。1962年至1990年期间,我院共治疗了15名儿童。同期因高血压前来我院检查的患者中,有1%被发现患有嗜铬细胞瘤。大多数患者患有高血压。高血压强度各异,约半数患者为阵发性。已有许多关于单侧、双侧、肾上腺外、家族性和复发性嗜铬细胞瘤的儿科病例报道。我们回顾了28年来对该肿瘤的治疗经验,并重点关注其诊断、术前及手术管理以及多发性内分泌肿瘤综合征的发生情况。