1.A case of Addison's disease.
Kwang Suk KANG ; Chull Wan IHM
Korean Journal of Dermatology 1991;29(4):538-543
No abstract available.
Addison Disease*
2.A case of Addison's disease.
Baek Gil LEE ; Hyang Sook LEE ; Il Kyung KIM ; Ho SEONG ; Chang Hee CHOI
Journal of the Korean Pediatric Society 1992;35(7):989-994
No abstract available.
Addison Disease*
3.A Case of Addison's Disease.
In Hoon LEE ; Yung Tak LIM ; Hee Ju JEON ; Chan Yung KIM
Journal of the Korean Pediatric Society 1988;31(12):1689-1695
No abstract available.
Addison Disease*
4.Tuberculous Addison's disease.
Hyun Joo BYUN ; Sai Hyun PAIK ; dong Seop CHOI
Journal of Korean Society of Endocrinology 1991;6(1):100-103
No abstract available.
Addison Disease*
5.A case of Addison's disease with hyperkalemic neuromyopathy.
Kyoung Tae BAE ; Seung Guel LEE ; Young Sung KIM ; Yi Kyoung SUNG ; Houng Gun PARK ; Yong Gu OH ; Se Gil KI
Journal of Korean Society of Endocrinology 1991;6(1):82-87
No abstract available.
Addison Disease*
6.A case of Addison's disease.
Cheol Hee HWANG ; Dong Kui LEE ; Myung Sug NAM ; Mun Ki CHO
Journal of the Korean Pediatric Society 1991;34(8):1169-1174
No abstract available.
Addison Disease*
7.Acute adrenal insufficiency as the primary manifestation of extrapulmonary tuberculosis: A case report
Herman Trianto ; Nurria Betty ; Laksmi Sasiarini ; Rulli Rosandi ; Putu Arsana ; Djoko Soeatmadji ; Achmad Rudijanto
Journal of the ASEAN Federation of Endocrine Societies 2016;31(1):59-64
Acute adrenal insufficiency (AI) is a life-threatening condition. While Addison’s disease (AD) is rare, in developing countries, tuberculosis (TB) still remains as the primary cause in 7 to 20% of cases. Urinary TB is also the third most common form of extrapulmonary disease. We report a case of 37-year-old male who presented with weakness, anorexia, weight loss, dysuria, flank pain and low grade fever. Examination revealed hypotension, hyperpigmentation, hyponatremia, hypoglycemia and low serum cortisol. He was diagnosed to have adrenal crisis due to Addison’s disease and extrapulmonary TB manifesting as urinary tract infection (UTI). He was treated with corticosteroids and anti-TB medications. Urologic reconstructive surgery was subsequently planned.
Addison Disease
;
Tuberculosis
8.A Case of Addison's Disease: Partial Recovery of Adrenocortical Function Following Antituberculous Medication.
Kang Seo PARK ; Jong Il JUN ; Kyung Keun CHO ; Mi Sook KIM ; Jin Man HUH ; Man Soon BAEK ; Moon Jun NA
Journal of Korean Society of Endocrinology 1997;12(4):642-646
Addisons disease is relatively rare than secondary adrenal insufficiency and result from progressive adrenocortical destruction. The common causes are idiopathic autoimmune atrophy and tuberculosis of adrenal glands. It is generally regarded as incurable in the sense that substitution therapy is required for the rest of the patients life. We report a case of tuberculous primary adrenal insufficiency which was confirmed by biopsy. This case was treated with antituberculous medication and showen to have improved adrenocortical function after six months.
Addison Disease*
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Adrenal Glands
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Adrenal Insufficiency
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Atrophy
;
Biopsy
;
Humans
;
Tuberculosis
9.A case of Addison's disease due to tuberculosis: pathologic confirmation by laparoscopic biopsy.
Ja Young LEE ; Jee Hee KIM ; Dong Joon LIM ; Sung Dae MOON ; Je Ho HAN
Korean Journal of Medicine 2008;75(6):704-708
Addison's disease is a rare disorder that is characterized by primary adrenal hypofunction and the underlying causes are various according to geographic regions. In order to establish an appropriate therapeutic regimen to treat adrenal insufficiency associated with Addison's disease, knowledge of the underlying adrenal abnormality is essential. We report a case of a 37-year-old man who showed biochemical evidence of adrenocortical insufficiency without signs of tuberculosis. Computed tomography showed bilateral adrenal enlargement and definitive diagnosis of adrenal tuberculosis was established by laparoscopic biopsy.
Addison Disease
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Adrenal Insufficiency
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Adult
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Biopsy
;
Humans
;
Tuberculosis
10.A Case of Isolated ACTH Deficiency
Sang Jin KIM ; Kyung Mook CHOI ; Sei Hyun BAIK ; Dong Seop CHOI
Journal of Korean Society of Endocrinology 1995;10(4):445-450
solated ACTH deficiency is a very uncommon cause of hypoadrenocorticism, with less than 200 cases reported in the literatures. The clinical presentation can be similar to that of primary adrenal insufficiency, but there is a greater tendency for hypoglycemia and absence of hyperpigmentation. The diagnosis is established by demonstrating hypocortisolism with undetectable serum levels of ACTH, normal adrenal responsiveness to prolonged ACTH infusion, and an absent ACTH response to insulin-induced hypoglycemia. Other endocrine function is normal.We experienced a case of isolated ACTH deficiency in 34 years old female who was admitted due to fever and drowsy mentality.So we present this case with a review of literatures.
Addison Disease
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Adrenocorticotropic Hormone
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Diagnosis
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Female
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Fever
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Humans
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Hyperpigmentation
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Hypoglycemia