Moretti A, Minuto M, Berti P, Bernini G P, Mannelli M, Miccoli P
Department of Internal Medicine, University of Pisa, 56100 Pisa, Italy.
J Endocrinol Invest. 2006 Sep;29(8):738-41. doi: 10.1007/BF03344185.
The association of pheochromocytoma (PHEO) and pregnancy is uncommon and life threatening for both the fetus and the mother. Early diagnosis and treatment is essential to decrease maternal and fetal mortality and to differentiate the disease from the more common pre-eclampsia. While medical treatment should be started immediately after diagnosis, the timing of surgical treatment is still debated. We describe the case of a 27-yr-old woman in the 18th week of pregnancy who showed a biochemical pattern typical of PHEO and, by imaging studies, 2 tumors with the same characteristics: the first localized on the right adrenal gland, the second at the right renal hilum. The patient underwent surgery because of suspicion of malignant PHEO with local metastasis, while histology revealed a rare association of a solitary PHEO and para-aortic neurofibroma, both tumors embryologically deriving from a common cell precursor.
嗜铬细胞瘤(PHEO)与妊娠相关的情况并不常见,且对胎儿和母亲均有生命威胁。早期诊断和治疗对于降低母婴死亡率以及将该疾病与更常见的先兆子痫相鉴别至关重要。虽然诊断后应立即开始药物治疗,但手术治疗的时机仍存在争议。我们描述了一名27岁妊娠18周女性的病例,该患者呈现出典型的PHEO生化模式,经影像学检查发现有2个具有相同特征的肿瘤:第一个位于右肾上腺,第二个位于右肾门。由于怀疑为伴有局部转移的恶性PHEO,该患者接受了手术,而组织学检查显示为罕见的孤立性PHEO与主动脉旁神经纤维瘤并存,这两种肿瘤在胚胎学上均源自共同的细胞前体。