Kwon Hyuk-Sang, Kim Sang-Il, Yoo Soon-Jib, Yoon Kun-Ho, Lee Kwang-Woo, Kang Moon-Won, Son Ho-Young, Kang Sung-Koo, Cha Bong-Yun
Department of Internal Medicine, College of Medicine, The Catholic University of Korea.
Endocr J. 2006 Apr;53(2):219-23. doi: 10.1507/endocrj.53.219.
Cushing's disease is a disorder of hypercortisolism caused by a pituitary micro- or macro-adenoma. Most patients with Cushing's disease have a bilateral adrenal enlargement, which depends on the duration of the disease, as a result of the long standing ACTH stimulation of both adrenal glands. However, in macronodular adrenocortical hyperplasia (MNH) that is caused by Cushing's disease, if the MNH gains autonomy, a bilateral adrenalectomy, as well as the removal of pituitary adenoma, is often essential. We encountered a patient diagnosed with Cushing's disease with bilateral adrenal tuberculosis simulating MNH. She had taken anti-tuberculosis medications one year prior to admission due to spinal tuberculosis. Sellar MRI revealed a pituitary macroadenoma, but adrenal CT showed enlargement in both adrenal glands that appeared to be MNH. A hormonal study and bilateral inferior petrosal sinus sampling revealed Cushing's disease. Therefore, she underwent trans-sphenoidal surgery of the pituitary mass. The pituitary surgery was successful and the serum cortisol returned to normal range. However, the adrenal mass rapidly enlarged after removing the pituitary tumor without showing evidence of a recurrence or adrenal autonomy of hypercortisolism. Accordingly, a laparoscopic left adrenalectomy was performed to examine the nature of the mass. The resected left adrenal gland was pathologically determined to have a lesion of tuberculosis with some part of the intact cortex. So we assumed that the cause of rapid adrenal enlargement might be due to adrenal tuberculosis. In summary, to the best of our knowledge, this is the first case of Cushing's disease coexisting with both adrenal tuberculosis simulating a bilateral MNH.
库欣病是一种由垂体微腺瘤或大腺瘤引起的皮质醇增多症。大多数库欣病患者双侧肾上腺增大,这取决于疾病的持续时间,是由于双侧肾上腺长期受到促肾上腺皮质激素(ACTH)刺激的结果。然而,在由库欣病引起的大结节性肾上腺皮质增生(MNH)中,如果MNH获得自主性,双侧肾上腺切除术以及垂体腺瘤切除术通常是必要的。我们遇到一名被诊断为库欣病的患者,其双侧肾上腺结核模拟MNH。她因脊柱结核在入院前一年服用了抗结核药物。蝶鞍磁共振成像(MRI)显示垂体大腺瘤,但肾上腺CT显示双侧肾上腺增大,看似MNH。激素研究和双侧岩下窦取样显示为库欣病。因此,她接受了垂体肿块的经蝶窦手术。垂体手术成功,血清皮质醇恢复到正常范围。然而,切除垂体肿瘤后肾上腺肿块迅速增大,未显示高皮质醇血症复发或肾上腺自主性的证据。因此,进行了腹腔镜左肾上腺切除术以检查肿块的性质。切除的左肾上腺经病理检查确定有结核病变,部分皮质完整。所以我们推测肾上腺迅速增大的原因可能是肾上腺结核。总之,据我们所知,这是首例库欣病与双侧肾上腺结核并存并模拟双侧MNH的病例。