1.A Case of Cushing's Syndrome Presenting as Endometrial Hyperplasia.
Sang Min LEE ; Jong Ryeal HAHM ; Tae Sik JUNG ; Jung Hwa JUNG ; Mi Yeon KANG ; Sun Joo KIM ; Soon Il CHUNG
The Korean Journal of Internal Medicine 2008;23(1):49-52
We describe here the case of a 39-year-old woman with a cortisol-producing adrenal adenoma and she presented with endometrial hyperplasia and hypertension without the specific characteristics of Cushing's syndrome. The patient had consulted a gynecologist for menometrorrhagia 2 years prior to her referral and she was diagnosed with endometrial hyperplasia and hypertension. Her blood pressure and the endometrial lesion were refractory despite taking multiple antihypertensives and repetitive dilation and curettage and progestin treatment. On admission, the clinical examination revealed mild central obesity (a body mass index of 22.9 kg/m2, a waist circumference of 85 cm and a hip circumference of 94cm), but there was no hirsutism and myopathy. She showed impaired glucose tolerance on an oral glucose tolerance test. The biochemical hypercortisolemia together with the prolactin and androgen levels were evaluated to explore the cause of her anovulation. Adrenal Cushing's syndrome was confirmed on the basis of the elevated urinary free cortisol (454 microgram/24h, normal range: 20-70) with a suppressed ACTH level (2.0 pg/mL, normal range: 6.0-76.0) and the loss of circadian cortisol secretion. A CT scan revealed a 3.1 cm, hyperechoic, well-marginated mass in the left adrenal gland. Ten months post-adrenalectomy, the patient had unintentionally lost 9 kg of body weight, had regained a regular menstrual cycle and had normal thickness of her endometrium.
Adrenal Cortex Neoplasms/complications/*diagnosis/surgery
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Adrenalectomy
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Adrenocortical Adenoma/complications/*diagnosis/surgery
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Adrenocorticotropic Hormone/blood
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Adult
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Circadian Rhythm
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Cushing Syndrome/*diagnosis/etiology/physiopathology
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Diagnosis, Differential
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Endometrial Hyperplasia/*diagnosis
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Female
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Humans
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Hydrocortisone/secretion/urine
2.Massive Thoracoabdominal Aortic Thrombosis in a Patient with Iatrogenic Cushing Syndrome.
Dong Hun KIM ; Dong Hyun CHOI ; Young Min LEE ; Joon Tae KANG ; Seung Seok CHAE ; Bo Bae KIM ; Young Jae KI ; Jin Hwa KIM ; Joong Wha CHUNG ; Young Youp KOH
Korean Journal of Radiology 2014;15(5):637-640
Massive thoracoabdominal aortic thrombosis is a rare finding in patients with iatrogenic Cushing syndrome in the absence of any coagulation abnormality. It frequently represents an urgent surgical situation. We report the case of an 82-year-old woman with massive aortic thrombosis secondary to iatrogenic Cushing syndrome. A follow-up computed tomography scan showed a decreased amount of thrombus in the aorta after anticoagulation therapy alone.
Aged, 80 and over
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Anticoagulants/therapeutic use
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Aorta, Abdominal/ultrasonography
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Cushing Syndrome/*complications/*diagnosis
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Electrocardiography
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Female
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Humans
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Iatrogenic Disease
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Thrombosis/*diagnosis/drug therapy/*etiology
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Tomography, X-Ray Computed
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Treatment Outcome
3.Subclinical Cushing's syndrome:analysis of diagnosis and surgical effect.
Chao FENG ; Han-Zhong LI ; He XIAO ; Wei-Gang YAN ; Yong-Qiang LI ; Wei-Feng XU
Chinese Journal of Surgery 2007;45(24):1691-1693
OBJECTIVETo improve the diagnostic and therapeutic ability on subclinical Cushing's syndrome.
METHODSRetrospective analysis for the clinical data of 24 cases of subclinical Cushing's syndrome, the clinical and biological characters pre and post operation were compared.
RESULTSNone of the 24 cases of subclinical Cushing's syndrome had the classic symptoms and signs of Cushing's syndrome. The common symptoms of these patients were hypertension in 17 cases, diabetes mellitus in 11 cases, hyperlipidemia in 9 cases, high plasma cortisol value in 13 cases and high 24 h UFC value in 9 cases. None of patients did respond to low dose dexamethasone suppression test, but 16 cases of them did not respond to high dose dexamethasone suppression test. All the cases were found adrenal tumors by CT scan, 10 cases in left adrenal and 14 cases in right adrenal. All the patients underwent retroperitoneal laparoscopic operation and were pathologic diagnosed to adrenal adenomas. During follow-up, the symptoms of 20 cases (83.3%) were cured after surgery, and hormone supplement was required in 8 cases.
CONCLUSIONSSubclinical Cushing's syndrome may be incidentally detected on clinical manifestations, laboratory findings and imaging examinations. CT scan, assays of plasma cortisol, urinary free cortisol and dexamethasone suppression test are most useful in the diagnosis. The potential benefit of surgery should be considered in those who have a definite diagnosis of subclinical Cushing's syndrome. Hormone supplement is required in some patients. It is safe and practical to perform retroperitoneal laparoscopic surgery on the patients with subclinical Cushing's syndrome.
Adrenal Cortex Neoplasms ; complications ; surgery ; Adrenalectomy ; methods ; Adrenocortical Adenoma ; complications ; surgery ; Adult ; Cushing Syndrome ; diagnosis ; etiology ; surgery ; Female ; Follow-Up Studies ; Humans ; Laparoscopy ; Male ; Middle Aged ; Retrospective Studies ; Treatment Outcome
4.A functioning adrenal adenoma and pheochromocytoma in the same adrenal gland: two discrete adrenal incidentalomas.
Ga Eun PARK ; Yoon Young CHO ; Yun Soo HONG ; Su Hoon KANG ; Kyung Ho LEE ; Hyun Woo LEE ; Jae Hyeon KIM
The Korean Journal of Internal Medicine 2015;30(1):114-117
No abstract available.
Adrenal Cortex Function Tests
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*Adrenal Cortex Neoplasms/complications/diagnosis/metabolism/surgery
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*Adrenal Gland Neoplasms/complications/diagnosis/metabolism/surgery
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Adrenalectomy
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*Adrenocortical Adenoma/complications/diagnosis/metabolism/surgery
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Biopsy
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Cushing Syndrome/diagnosis/etiology
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Female
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Humans
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Immunohistochemistry
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*Incidental Findings
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Middle Aged
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*Neoplasms, Multiple Primary/complications/diagnosis/metabolism/surgery
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*Pheochromocytoma/complications/diagnosis/metabolism/surgery
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Predictive Value of Tests
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Tomography, X-Ray Computed
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Treatment Outcome
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Tumor Markers, Biological/metabolism