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Jae Ho Choi  (Choi JH) 2 Articles
A Case of Primary Adrenal Insufficiency in a Patient with Acquired Immunodeficiency Syndrome.
Jae Ho Choi, Suk Chon, Yu Chul Hwang, Jun Seong Son, Seung Joon Oh, Kyu Jeung Ahn, Ho Yeon Chung, Jeong Taek Woo, Sung Woon Kim, Jin Woo Kim, Young Seol Kim, In Kyung Jeong
Endocrinol Metab. 2011;26(3):253-257.   Published online September 1, 2011
DOI: https://doi.org/10.3803/EnM.2011.26.3.253
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  • 1 Crossref
AbstractAbstract PDF
The adrenal gland is the most commonly involved endocrine organ in patients infected with the human immunodeficiency virus (HIV). Adrenal function abnormality is more common in HIV patients than in the general population. It is important to recognize the condition of adrenal insufficiency, as this adrenal disorder may prove fatal if left untreated. Herein, we report a case of primary adrenal insufficiency in a 37-year-old male patient with acquired immunodeficiency syndrome. The patient complained of fever, general weakness, and fatigue. Impaired adrenal function was noted in the rapid ACTH stimulation test. After steroid supplementation, the patient's symptoms were improved. Therefore, HIV care physicians should ascertain adrenal dysfunction in HIV patients when they complain of fever and general weakness.

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  • A Case Report of Adrenal Insufficiency Treated with Korean Medicine
    Young-ji Kim, Jung-yeon Kwon, Ho-yeon Go, Kyung-hwan Kong
    The Journal of Internal Korean Medicine.2017; 38(5): 583.     CrossRef
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A Case of Adrenocortical Carcinoma Secreting Cortisol, Androgen and Aldosterone.
Jae Ho Choi, Ye Ri So, Yu Chul Hwang, In Kyung Jeong, Kyu Jeung Ahn, Ho Yeon Chung, Seung Ae Yang
Endocrinol Metab. 2011;26(3):239-242.   Published online September 1, 2011
DOI: https://doi.org/10.3803/EnM.2011.26.3.239
  • 2,315 View
  • 34 Download
  • 1 Crossref
AbstractAbstract PDF
Primary adrenocortical carcinoma is a rare tumor, and is characterized by a peri-tumor mass effect and hormone excess signs. Adrenocortical carcinoma most commonly secretes cortisol, but tumors that secrete other adrenal hormones (aldosterone, androgen) are rare. Herein, we report the case of a 70-year-old woman with cortisol, androgen, and aldosterone-secreting adrenal carcinoma. The patient complained of generalized weakness, moon face, and central obesity. On laboratory examination, hypokalemia and metabolic alkalosis was detected. On the hormone test, cortisol, DHEA-S, and aldosterone were all increased. Abdominal CT showed a large right adrenal mass. She underwent right adrenalectomy and the histology revealed the presence of an adrenocortical carcinoma. After adrenalectomy, the patient was treated with hydrocortisone and mitotane.

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  • A Case of Adrenocortical Carcinoma Secreting Cortisol and Aldosterone
    Jiyoon Ha, Min Kyung Kim, Yoon Jin Cha, Seung Kyu Kim, Gi Young Yun, Kwangwon Rhee, Joon Seong Park, Eun-Suk Cho, Chul Woo Ahn, Jong Suk Park
    Yeungnam University Journal of Medicine.2012; 29(2): 132.     CrossRef
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