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首页> 外文期刊>Japanese heart journal >Familial Bilateral Pheochromocytoma with Medullary Carcinoma of the ThyroidThe Second Kindred of Familial Pheochromocytoma in Japan
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Familial Bilateral Pheochromocytoma with Medullary Carcinoma of the ThyroidThe Second Kindred of Familial Pheochromocytoma in Japan

机译:家族性双性嗜铬细胞瘤与甲状腺髓样癌日本的第二类家族性嗜铬细胞瘤

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The second kindred of familial pheochromocytoma in Japan was reported. Bilateral pheochromocytomas were found in the elder and the youngest sister. In the other members of this family, no pheochromocytoma and thyroid tumor was found. Medullary thyroid carcinoma was removed before adrenalectomy in both patients. Diagnostic and therapeutic problems in these cases were discussed. It was our conclusion that once pheochromocytoma, especially in bilateral, or thyroid tumor has been found in either normotensive or hypertensive patients, other members of the family as well as the patient should be examined carefully for similar tumors. Tyramine test was less valuable for screening of paroxysmal type of pheochromocytoma.
机译:据报道日本有第二类家族性嗜铬细胞瘤。在姐姐和姐姐中发现了双边嗜铬细胞瘤。在该家族的其他成员中,未发现嗜铬细胞瘤和甲状腺肿瘤。两名患者均在肾上腺切除术前去除了甲状腺髓样癌。讨论了这些情况下的诊断和治疗问题。我们的结论是,一旦在血压正常或高血压的患者中发现了嗜铬细胞瘤,尤其是在双侧或甲状腺肿瘤中,则应仔细检查该家族的其他成员以及该患者是否患有类似的肿瘤。酪胺试验对阵发性嗜铬细胞瘤类型筛查的价值较小。

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