Djema A I, Mahmoud M D, Collin P, Heymann M F
Service de néphrologie, Centre hospitalier de Cholet.
Nephrologie. 1998;19(3):121-3.
Parathyroid cancer is very rare in chronic renal failure. Only twelve cases have been described, but the actual incidence might be under estimated. Monoclonal proliferation have been demonstrated in hyperplasic parathyroid glands of uremic patients and the diagnosis between benign or malignant tumor may be difficult. Evidence for a deletion of the "Retinoblastoma Tumor Suppressor gene" (RB gene) is helpful for the diagnosis of parathyroid cancer, especially in the absence of dissemination. A 46-years old male patient on dialysis since 1989 for polycystic kidney disease developed a refractory and persistent hyperparathyroidism after parathyroidectomy with vascular and osteoarticular complications. Liver nodules were localised by sestaultrasonography. MIBI radionucleid scan and were confirmed by CT-scan, and ultrasonography. Diagnosis of parathyroid cancer was confirmed by the immuno-histochemical study of the biopsied liver nodules and the histopathological review of the removed parathyroid glands.
甲状旁腺癌在慢性肾衰竭中非常罕见。仅报道过12例,但实际发病率可能被低估。在尿毒症患者增生的甲状旁腺中已证实有单克隆增殖,良性或恶性肿瘤的诊断可能很困难。“视网膜母细胞瘤抑癌基因”(RB基因)缺失的证据有助于甲状旁腺癌的诊断,尤其是在无播散的情况下。一名46岁男性患者自1989年起因多囊肾病接受透析治疗,甲状旁腺切除术后出现难治性持续性甲状旁腺功能亢进,并伴有血管和骨关节并发症。通过 sestaultrasonography定位肝脏结节。MIBI放射性核素扫描,并经CT扫描和超声检查证实。通过对活检的肝脏结节进行免疫组织化学研究以及对切除的甲状旁腺进行组织病理学检查,确诊为甲状旁腺癌。