From the year 1989 to December 1994, 59 patients with Cushing syndrome (12 males, 47 females aged 15-46) were investigated. Clinical symptoms: central obesis, round face, weakness, high blood pressure, cracked skin, mental disorder, acnea, hirsulism. Laboratory examinations: high level of urine 17OHCS, cortisol secretion increasing in 8 and 20 o’clock and loss of secretion. Morphological examinations: X-ray radiography of hypophysal hole, ultrasound of surrenal gland, CT scan of hypophysal hole. Causes: 79.7% is Cushing disease, 11.8% adenoma od surrenal gland, 8.5% surrenal cancer
Cushing Syndrome ; diagnosis ; epidemiology

No abstract available.
Cushing Syndrome* ; Diagnosis* ; Diagnosis, Differential*

A 28-year old female was diagnosed preoperatively to have a pheochromocytoma producing ACTH at other hospital. However the operation was delayed due to poor general condition and abnormal liver function. She revealed severe hypercortisolism, hypokalemic metabolic alkalosis, glucose intolerance and showed rapid downhill course. She was transferred to our hospital for operation but septic complications were strarted already. She was not recovered in spite of desperate operation and died just after moribund discharge. ACTH producing pheochromocytoma is uncommon and literature review indicated high mortality rates due to improper preoperative diagnosis. Proper preoperative recognition and early surgical management is mandatory for better results.
ACTH Syndrome, Ectopic* ; Adrenocorticotropic Hormone ; Alkalosis ; Cushing Syndrome ; Diagnosis ; Female ; Glucose Intolerance ; Humans ; Liver ; Mortality ; Pheochromocytoma*

Neuroendocrine tumors of the gallbladder are rare, and typically found incidentally after a cholecystectomy. Few data are available on adrenocorticotrophic hormone (ACTH)-producing neuroendocrine tumors originating specifically from the gallbladder. We experienced the case of a patient with a gallbladder mass who presented with Cushing's syndrome, who was subsequently diagnosed as an ACTH-producing neuroendocrine carcinoma of the gallbladder. Despite being rare, hormone-producing neuroendocrine tumors should be part of the differential diagnosis in patients with Cushing's syndrome.
ACTH Syndrome, Ectopic ; Adrenocorticotropic Hormone ; Carcinoma, Neuroendocrine* ; Cholecystectomy ; Cushing Syndrome* ; Diagnosis, Differential ; Gallbladder* ; Humans ; Neuroendocrine Tumors

Myxoid variant of adrenal cortical carcinoma is extremely rare and there have been only 16 such cases reported in the medical literature. Here we report on a case of 43-year-old woman with a left adrenal mass that was detected during the evaluation for Cushing's syndrome. Left adrenalectomy was performed and the tumor weighed 347 g. The cut surface was predominantly myxoid and gelatinous with central hemorrhage and necrosis. Histologically, the tumor cells were rather small, uniform and polygonal with mild pleomorphism. It showed diverse morphologic patterns according to the amount of the myxoid stromal component. Making the diagnosis was not easy because the tumor was without areas of conventional adrenocortical carcinoma. Immunohistochemically, the tumor cells were positive for alpha-inhibin, synaptophysin and vimentin, but the tumor cells were negative for pan-cytokeratin and CAM 5.2. The immunophenotypes were identical to those of conventional adrenal cortical neoplasms. During the evaluation of a cytokeratin-negative and vimentin-positive retroperitoneal neoplasm with a myxoid component, the possibility of adrenal cortical tumor should be considered in spite that this is a very rare entity.
Adrenalectomy ; Adrenocortical Carcinoma* ; Adult ; Cushing Syndrome ; Diagnosis ; Female ; Gelatin ; Hemorrhage ; Humans ; Necrosis ; Retroperitoneal Neoplasms ; Synaptophysin ; Vimentin

Diagnostic accuracy in localizing tumors by means of computed tomography (CT), adrenal scintigraphy, ultrasonography (US) and IVP was compared in 12 cases of adrenal tumors which were experienced during last 6 years. The following results were obtained : 1. The patient group consists of 8 pheochromocytomas, 3 primary aldosteronism, and 1 Cushing syndrome. 2. For the initial diagnosis of adrenal cortical tumor (primary aldosteronism, Cushing syndrome) CT and adrenal scintigraphy are reliable and noninvasive modalities with high diagnostic accuracy, whereas in pheochromocytoma, US, CT and adrenal scintigraphy was useful. 3. Invasive diagnostic modalities such as aortography, venous sampling of adrenal gland and venography should be restricted to localizing adrenal tumors cannot be diagnosed by previous non -invasive diagnostic modalities.
Adrenal Glands ; Aortography ; Cushing Syndrome ; Diagnosis ; Humans ; Hyperaldosteronism ; Pheochromocytoma ; Phlebography ; Radionuclide Imaging ; Ultrasonography

Between 1980 and 1989, our experience of surgical management with 21 adrenal diseases was presented. There were 3 cases of Cushing's syndrome, 3 of primary aldosteronism, 6 of pheochromo cytoma, 5 of neuroblastoma, 2 of extraadrenal paraganglioma, 1 of adrenocortical carcinoma and 1 of adrenal cyst. The use of advanced radiographic and laboratory procedures resulted in the refinement of diagnosis and localization of tumors, enabling better surgical management of adrenal disorders. Among those, 19 cases underwent unilateral adrenalectomy and 2 cases of Cushing's disease underwent bilateral adrenalectomy. Surgical approaches to the adrenal gland were transperitoneal in 16 cases and extraperitoneal in 5 cases. Operative complications occurred in 11 cases. The incidence, however, of complications related to the operative approach was not significant except in 2 cases of postoperative ileus.
Adrenal Glands ; Adrenalectomy ; Adrenocortical Carcinoma ; Cushing Syndrome ; Diagnosis ; Hyperaldosteronism ; Ileus ; Incidence ; Neuroblastoma ; Paraganglioma

PURPOSE: To examine and compare the perioperative outcomes of laparoscopic adrenalectomy (LA) and to determine its efficacy in patients with nonfunctioning adrenal adenomas (NFA) and subclinical Cushing syndrome (SCS). MATERIALS AND METHODS: We retrospectively analyzed the clinical data obtained from 79 consecutive patients who underwent LA for the treatment of either NFA (n=35) or SCS (n=44) between 2011 and 2016. All patients had undergone computed tomography, as well as endocrinological tests to confirm the diagnosis prior to the adrenalectomy. The primary endpoint was improved metabolic parameters relating to diabetes, hypertension, dyslipidemia, and obesity. RESULTS: Patients with SCS compared to those with NFA showed a higher occurrence of diabetes (29.5% vs. 11.4%), hypertension (59.1% vs. 34.3%), and dyslipidemia (43.2% vs. 14.3%). Patients with SCS showed a smaller median tumor size compared to those with NFA (2.5 cm vs. 5 cm). No significant perioperative complications ≥ Clavien-Dindo classification grade III were observed in any patient (SCS or NFA group). In terms of their metabolic profile, patients with SCS showed a significant postoperative improvement in hypertension (50.0%), diabetes (53.9%), dyslipidemia (31.6%), and obesity (29.2%). However, patients with NFA showed a postoperative improvement only in dyslipidemia (40.0%) and obesity (4.8%). CONCLUSIONS: Owing to absence of significant perioperative complications and the marked postoperative improvement in metabolic impairment, LA is a useful treatment strategy in patients diagnosed with SCS. In contrast, LA was not observed to show beneficial effects in correcting/improving the metabolic profile in patients presenting with NFA.
Adenoma* ; Adrenalectomy* ; Classification ; Cushing Syndrome* ; Diagnosis ; Dyslipidemias ; Humans ; Hypertension ; Metabolome ; Obesity ; Retrospective Studies

Cryptococcosis is a disease caused by Cryptococcus neoformans, that most commonly affects immunosuppressed patients. Cutaneous cyptococcosis occurs in 10-15% of disseminated cases and its clinical manifestation is variable. We have presented an unusual manifestation of cutaneous cryptococcosis in a patient with iatrogenic Cushing syndrome. Clinically, the ulcers were considered to be pyoderma gangrenosum but the tissue biopsy and culture revealed cryptococcosis. This case illustrates that in making the diagnosis of pyoderma gangrenosum, one must exclude deep fungal infection.
Biopsy ; Cryptococcosis* ; Cryptococcus neoformans ; Cushing Syndrome ; Diagnosis ; Humans ; Pyoderma Gangrenosum* ; Pyoderma* ; Ulcer

In order to differentiate the causes of Cushing's syndrome; whether it is pituitary or adrenal-dependent, a high dose dexamethasone suppression test is usually performed but this does not always correlated with the imaging diagnosis. We report a case of bilateral macronodular adrenal hyperplasia, which was thought to be independent to adrenocorticotrophin (ACTH) stimulation. At first we thought it was pituitary-dependent Cushing's syndrome, due to its suppression by high dose dexamethasone. However, we found no abnormal findings on the brain sella magnetic resonance image (MRI). A significant finding, however, we found bilateral adrenal masses on the abdominal computed tomography (CT). We performed percutaneous selective adrenal venous sampling (PSAVS), and confirmed hypercortisolism of the left adrenal mass only. Therefore, we decided to remove the left adrenal gland to preserve the residual function of the right adrenal gland. After the left adrenalectomy, the patient became normotensive, and their buffalo hump disappeared, and her 24 hour urinary free cortisol level returned to normal.
Adrenal Glands ; Adrenalectomy* ; Brain ; Buffaloes ; Cushing Syndrome* ; Dexamethasone ; Diagnosis ; Humans ; Hydrocortisone ; Hyperplasia*